Author: Marianne Halterman

  • Kids Preferred Recalls “My First” Disney-Character Figurines Due to Choking Hazard

    Recall Date: February 16, 2023

    Recall number: 23-127

    Recall Summary

    Name of Product: “My First” Mickey Mouse, Minnie Mouse, Buzz Lightyear, and Stitch Figurines

    Hazard: The arms or legs on the figurines can detach, posing a small part choking hazard to children.

    Remedy: Refund

    Consumer Contact: Kids Preferred toll-free at 888-968-9268 from 8:30 a.m. to 5 p.m. ET Monday through Friday, email at recall@kidspreferred.com or online at https://kidspreferred.com/pages/recall-safety-announcements or www.kidspreferred.com and click “Recall Information” on the bottom of the page for more information.

    Recall Details

    Units: About 16,140 (in addition, about 600 were sold in Canada)

    Description: This recall involves soft vinyl figurines of the following Disney characters: Mickey Mouse, Minnie Mouse, Buzz Lightyear, and Stitch. Some of the figurines have a bead rattle. They measure about 4.25 to 5.25 inches high.

    Remedy: Consumers should immediately take the recalled toys away from children and contact Kids Preferred for instructions on receiving a full refund.  Consumers who register for the recall will receive a pre-paid shipping label to return the product to the Firm for a full refund. 

    Incidents/Injuries: The firm has received 10 reports of small parts detaching from the figurines. No injuries have been reported.

    Sold At: BuyBuy Baby and other toy, gift, and bookstores nationwide and online at amazon.com from May 2022 through December 2022 for between $15 and $19.

    Importer(s): Kids Preferred, of East Windsor, New Jersey

    Manufactured In: China

    Note: Individual Commissioners may have statements related to this topic.  Please visit www.cpsc.gov/commissioners to search for statements related to this or other topics.

  • Rear Facing Infant Seat Webbing May Fail

    Recall Date: February 10, 2023

    Recall number: NHTSA Campaign Number 23C001000

    Recall Summary

    Name of Product: CHILD SEAT

    Hazard: 

    An infant seat belt with insufficient strength many not properly restrain the occupant, increasing the risk of injury in a crash.

    Remedy: 

    CTP/CYBEX will mail owners a replacement central seat belt adjuster strap assembly and installation instructions, free of charge. Owner notification letters are expected to be mailed March 13, 2023.

    Consumer Contact: Owners may contact CTP’s customer service at 1-937-415-3215.

    Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.nhtsa.gov.

    Recall Details

    Units: 31,080

    Description: 

    Columbus Trading-Partners USA, Inc. (CTP) is recalling certain Cybex models Aton, Aton Q, Aton M, Aton 2, and Cloud Q rear facing infant seats. Please refer to CTP’s recall report for specific model details. The design of the webbing for the central seat belt adjuster allows it to fray, which can reduce the strength of the seat belt. As such, these infant seats fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 213, “Child Restraint Systems” and 209, “Seatbelt Assemblies.”

    Affected Products (5) – CHILD SEAT

    CYBEXATON9999
    CYBEXATON 29999
    CYBEXATON M9999
    CYBEXATON Q9999
    CYBEXCLOUD Q9999

    Manufacturer: Columbus Trading-Partners USA, Inc.

    Associated Documents (3)

    Recall Acknowledgement
    RCAK-23C001-9644.pdf 647.149KB
    https://static.nhtsa.gov/odi/rcl/2023/RCAK-23C001-9644.pdf

    Recall 573 Report – February 15, 2023
    RCLRPT-23C001-3876.PDF 221.053KB
    https://static.nhtsa.gov/odi/rcl/2023/RCLRPT-23C001-3876.PDF

    Noncompliance Notice 573 Report
    RCLRPT-23C001-5162.PDF 220.836KB
    https://static.nhtsa.gov/odi/rcl/2023/RCLRPT-23C001-5162.PDF

  • CPSC and Baby Trend Warn Consumers About Entrapment Hazard with the Detachable Canopy on Baby Trend Sit N’ Stand Strollers; One Death Reported

    WASHINGTON, D.C. – The U.S. Consumer Product Safety Commission (CPSC) and Baby Trend are warning consumers about a risk of head or neck entrapment between the pivoting front canopy and the arm rest or seat back of Baby Trend’s Sit N’ Stand Double and Ultra strollers with model numbers beginning with “SS76” or “SS66”. 

    The space in front of and behind the strollers’ pivoting front canopy can entrap a child’s head or neck if a non-occupant child climbs on the exterior of the stroller or when a child in the front seat of the stroller is not securely restrained in the seat using all five points of the harness. Entrapment could lead to a loss of consciousness, serious injury, or death.

    Baby Trend has received one report of neck entrapment in the space between the front of the canopy tube and arm rest of a Baby Trend Sit N’ Stand double stroller, resulting in the asphyxiation death of a non-occupant 14-month-old whose father was nearby but unable to see the child. Baby Trend has also received one report of entrapment in the space between the back of the canopy tube and the seat back of the front seat, resulting in neck bruises to a 17-month-old child, who was partially secured. 

    Consumers can mitigate the hazard by removing and separately storing the canopy when not in use, not allowing children to play on the strollers, and always fully securing children in the strollers with the built-in five-point harness. 

    The Sit N’ Stand Double and Ultra strollers, model numbers beginning SS76 or SS66, have a black or silver frame and a black tray at the front with oval cutouts on the sides. “Sit N’ Stand” is printed in white on the sides of the frame. “Baby Trend” is printed on the side of the mesh basket under the seat. The model number is printed on a sticker located on the left inside rear of the frame, near the left rear axle. The Sit N’ Stand strollers have been sold nationwide since 2009.

    These strollers have been and are sold online at www.babytrend.comAmazon.combedbathandbeyond.com and other online retailers, and in stores including Walmart, Target, Kohl’s, and buybuy BABY.

    Instructions on how to remove the detachable canopy for Sit N’ Stand Double or Ultra strollers with model numbers beginning SS76 or SS66 are provided in the product manual and images accompanying this release.

    Consumers are encouraged to report incidents or injuries associated with the Baby Trend Sit N’ Stand Double or Ultra strollers or with any product to CPSC at www.SaferProducts.gov. Consumers are also encouraged to report incidents and direct questions regarding Baby Trend products to Baby Trend at 800-328-7363 from 9 a.m. to 4:30 p.m. Pacific Time Monday through Friday or by email at info@babytrend.com.

    Trend Sit N’ Stand Stroller
  • Multiple Children’s Clothing Recalls due to violation of Federal Flammability Standards

    These recalls were all issued on January 20, 2023, please click the titles for details and photographs. Additional information about recalls can be found at cpsc.gov.

  • Kids2 Reannounces Recall of 694,000 Rocking Sleepers; Four Additional Deaths After Recall

    Recall Date: January 09, 2023 (The original recall was announced in April 2019).

    Recall number: 23-089

    Recall Summary

    Name of Product: All models of Kids2 Rocking Sleepers

    Hazard: Infant fatalities have occurred in the Rocking Sleepers, after the infants rolled from their back to their stomach or side while unrestrained, or under other circumstances.

    Remedy: Refund

    Consumer Contact: Kids2 toll-free at 866-869-7954 from 8 a.m.to 5 p.m. ET Monday through Friday or visit Rocking Sleeper recall or www.kids2.com and click on “Recalls” for more information.

    Recall Details

    Units: About 694,000

    Description: All models of Kids2 Rocking Sleepers are included in this recall.

    Remedy: Consumers should stop using the rocking sleeper immediately and contact Kids2 for a refund. It is illegal to sell or distribute the recalled sleepers.

    Incidents/Injuries: A total of 15 infant fatalities were reported to have occurred in the Kids2 Rocking Sleepers, after the infants rolled from their back to their stomach or side while unrestrained, or under other circumstances. Eleven deaths were reported to have occurred before the recall, (including five deaths previously reported by CPSC and Kids2 at the time of the original recall). Four fatalities were reported to have occurred after the recall was announced. Kids2 notes that in some of the reports, it has been unable to confirm the circumstances of the incidents or that the product was a Rocking Sleeper.

    Sold At: Major retailers nationwide, including Walmart, Target and Toys “R” Us and online from March 2012 through April 2019 for between $40 and $80.

    Importer(s): Kids2, Inc. of Atlanta, Georgia

    Manufactured In: China

    Note: Individual Commissioners may have statements related to this topic.  Please visit www.cpsc.gov/commissioners to search for statements related to this or other topics.

  • Fisher-Price Reannounces Recall of 4.7 Million Rock ‘n Play Sleepers; At Least Eight Deaths Occurred After Recall

    Recall Date: January 09, 2023 (The original recall was announced on April 12, 2019.)

    Recall number: 23-088

    Recall Summary

    Name of Product: All models of Rock ‘n Play Sleepers

    Hazard: Infant fatalities have occurred in the Rock ‘n Play Sleepers, after the infants rolled from their back to their stomach or side while unrestrained, or under other circumstances.

    Remedy:  Refund

    Consumer Contact: Fisher-Price online at Rock ‘n Play Recall or www.mattel.com and click on “Recall & Safety” or toll-free at 866-812-6518 from 9 a.m. to 6 p.m. ET Monday through Friday for more information.

    Recall Details

    Units: About 4.7 million

    Description: All Rock ‘n Play Sleepers

    Remedy: Consumers should stop using the Rock ‘n Play immediately and contact Fisher-Price for a refund or voucher. It is illegal to sell or distribute the recalled sleepers.

    Incidents/Injuries: On April 12, 2019, at the time the original recall was announced, over 30 fatalities were reported to have occurred in the Rock ‘n Play Sleepers after the infants rolled from their back to their stomach or side while unrestrained, or under other circumstances. Since the recall, approximately 70 additional fatalities have been reported, which includes at least 8 fatalities that were reported to have occurred after the initial recall announcement. Approximately 100 deaths have reportedly occurred while infants were in the products. Fisher-Price notes that in some of the reports, it has been unable to confirm the circumstances of the incidents or that the product was a Rock ‘n Play Sleeper.

    Sold At: Major stores nationwide including Walmart, Target, and online at Amazon from September 2009 through April 2019 for between $40 and $149.

    Importer(s): Fisher-Price, of East Aurora, New York

    Manufactured In:  China

    Note: Individual Commissioners may have statements related to this topic.  Please visit www.cpsc.gov/commissioners to search for statements related to this or other topics.

  • Pacific Cycle Recalls Pacific Kids’ Igniter and Pacific Bubble Pop 20-Inch Bicycles Due to Fall Hazard; Sold Exclusively at Target

    Recall Date: December 22, 2022

    Recall number: 23-077

    Recall Summary

    Name of Product: Pacific Igniter and Pacific Bubble Pop 20″ kids’ bicycles

    Hazard: The bicycle’s handlebar can become loose during use, posing a fall hazard.

    Remedy: Repair

    Consumer Contact: Pacific Cycle toll-free at 877-564-2261 from 7 a.m. and 6 p.m. CT Monday through Friday, email at customerservice@pacific-cycle.com or online at www.pacific-cycle.com/safety-notices-recalls/ or www.pacific-cycle.com and click on “Safety Notices and Recalls” for more information.

    Recall Details

    Units: About 147,000

    Description: This recall involves two models of 20” Pacific Kids’ Bicycles. The Pacific Igniter has red with white and black accent colors and the word “Igniter” on the downtube and the Pacific Bubble Pop has pink with blue and black accent colors and the words “Bubble Pop” on the downtube. The model numbers 201230TG, 201231TG are located on the seat tube where it meets the bottom bracket.

    Remedy: Consumers should immediately stop riding the recalled bicycles and contact Pacific Cycle to receive a free repair kit, which will contain a bolt, nut, washer and grease packet with instructions to apply grease to the bolt.

    Incidents/Injuries: The firm has received 23 reports of incidents of the bicycle’s handlebars becoming loose during use. Ten injuries involving bruising and abrasions have been reported.

    Sold At: Target stores nationwide and online at www.target.com from July 2020 through September 2022 for about $140.

    Importer(s): Pacific Cycle Inc., of Madison, Wisconsin

    Manufactured In: China

    Note: Individual Commissioners may have statements related to this topic.  Please visit www.cpsc.gov/commissioners to search for statements related to this or other topics.

  • Target Recalls Children’s Pillowfort Weighted Blankets Due to Asphyxiation Hazard; Two Fatalities Reported

    Recall Date: December 22, 2022

    Recall number: 23-078

    Recall Summary

    Name of Product: Pillowfort™ Weighted Blankets

    Hazard: A young child can become entrapped by unzipping and entering the blanket, posing a risk of death by asphyxiation.

    Remedy: Refund

    Consumer Contact: Target at 800-440-0680 from 7 a.m. to 10 p.m. CT daily, or online at www.target.com and click on “Recall Information”, then on “Home Goods” for more information. Consumers can also click the “Products Recalls” tab on Target’s Facebook page for more information.

    Recall Details

    Units: About 204,000

    Description: This recall involves Pillowfort Weighted Blankets. The blankets weigh 6 pounds, measure 60 inches long and 40 inches wide and have a removable, waterproof, washable cover. The blankets come in eight prints or colors including unicorn white, space navy, pink, blue, gray, buffalo plaid red, blue constellation, and unicorn pink. Item numbers 097-02-0140 (Unicorn – White), 097-02-0148 (Space Navy), 097-02-0361(Pink), 097-02-0363 (Blue), 097-02-0364 (Gray), 097-02-1603 (Buffalo Plaid – Red), 097-02-3904 (Blue Constellation) and 097-02-3905 (Unicorn – Pink) are printed on the fabric tag attached to the removable covers of the blankets.

    Remedy: CPSC and Target are urging consumers to stop using the recalled weighted blankets immediately and contact Target for a refund.

    Incidents/Injuries: Target has received four reports of children becoming entrapped in these weighted blankets, including the two fatalities.

    Sold Exclusively At: Target stores nationwide and online at www.target.com. The blankets were sold from December 2018 through September 2022 for $40.

    Importer(s): 

    Manufactured In: China

    Note: Individual Commissioners may have statements related to this topic.  Please visit www.cpsc.gov/commissioners to search for statements related to this or other topics.

  • ByHeart Issues Voluntary Recall of Five Batches of Its Infant Formula Because of Possible Health Risk

    Summary

    Company Announcement Date: December 11, 2022

    FDA Publish Date: December 11, 2022

    Product Type: Food & Beverages

    Reason for Announcement: Potential for cross-contamination with Cronobacter sakazakii

    Company Name: ByHeart

    Brand Name: ByHeart

    Product Description: Whole Nutrition Infant Formula, Milk Based Powder with Iron for 0-12months

    Company Announcement

    None of the distributed ByHeart product has tested positive for any contaminants.

    No consumer complaints received, to date, that would indicate any illness.

    Recall is not related to ByHeart’s own manufacturing facility in Reading, PA in any way; facility continues to run 24/7; re-stock expected in January.

    ByHeartExternal Link Disclaimer, a next-generation baby nutrition company, announced today that, out of an abundance of caution, it has chosen to voluntarily recall five batches of ByHeart Whole Nutrition Infant Formula due to the potential for cross-contamination with Cronobacter sakazakii. No distributed ByHeart product has tested positive for the bacteria.

    The product being recalled is ByHeart Whole Nutrition Infant Formula, Milk Based Powder with Iron for 0-12 Months in 24 oz containers. The formula under voluntary recall was distributed directly to consumers in the U.S. and can be identified by the number on the bottom of the can. Recalled product batches are 22273 C1, 22276 C1, 22277 C1, 22278 C1, and 22280 C1 printed with use by 01 JAN 24 or 01JUL 24.

    Cronobacter bacteria can cause severe, life-threatening infections (sepsis) or meningitis (an inflammation of the membranes that protect the brain and spine). Symptoms of sepsis and meningitis may include poor feeding, irritability, temperature changes, jaundice (yellow skin and whites of the eyes), grunting breaths and abnormal movements. Cronobacter infection may also cause bowel damage and may spread through the blood to other parts of the body.

    It is important to note that this recall is not related to ByHeart’s own manufacturing in any way. In addition, the company has not received any consumer complaints that would indicate any illness, to date; illness complaints are an early detection of safety concerns. If a baby has already consumed all of the formula, there is no reason for concern, and no additional action is needed. If parents have any questions, they should consult with their pediatrician.

    ByHeart owns its entire manufacturing supply chain with the exception of final canning, which is conducted by a reputable third-party packager. ByHeart is taking this precautionary measure because one test sample collected from the third-party packaging facility tested positive for Cronobacter sakazakii. All product packaged that day, and the first production on the next day, was isolated for destruction and not distributed. Out of an abundance of caution, we are now recalling all product produced during the entire production run.

    As a company committed to parents, ByHeart holds itself to the highest standards when it comes to safety and applauds the FDA’s efforts to oversee the safe manufacturing of infant formula. Parents can remain confident in the safety of ByHeart’s products as the company continues to expand its investments in infant formula innovation, clinical studies, and industry-leading quality standards. ByHeart’s manufacturing facility in Reading, PA, continues to operate 24/7, and the company is committed to providing customers formula in January.

    What ByHeart Customers Should Do

    Customers who purchased ByHeart product should check the bottom of the can and dispose of product from batches 22273 C1, 22276 C1, 22277 C1, 22278 C1, and 22280 C1. ByHeart is setting up a webpage at https://byheart.com/noticesExternal Link Disclaimer with additional information about its measures. Should customers have any other questions or want to find out if the product they have is included in the voluntary recall, please email notices@byheart.com or text ByHeart at 1-909-506-2354. The company will also be reaching out directly to all customers via email who purchased orders from these identified batches.

    ByHeart knows that formula is critical to a baby’s health and growth and wants to make sure that all customers have what they need to keep their baby fed and healthy, no matter what brand of formula they use. While ByHeart works 24/7 to meet the demand for formula, the fastest way the company can replace the formula customers purchased is to cover the cost of two cans of alternate formula. Additionally, affected customers will receive two cans of their next order of ByHeart Whole Nutrition Formula for free.

    If your infant is experiencing symptoms related to Cronobacter infection, contact your health care provider to report their symptoms and receive immediate care. To report an illness or adverse event, you can


    Company Contact Information

    Consumers: ByHeart 1-909-506-2354 notices@byheart.com

    Product Photos are available at: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/byheart-issues-voluntary-recall-five-batches-its-infant-formula-because-possible-health-risk?utm_medium=email&utm_source=govdelivery#recall-photos