children product Recalls

266 recalls tagged with “children product”.

Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific NephroMax Kit Recall Covers 458 Units Over Foreign Material Migration Risk

Boston Scientific Corp. recalls 458 NephroMax Kit units using Encore 26 Inflation Devices after an internal review found foreign material particles could migrate from the inflation device into balloon dilatation catheters. The recall affects UPNs M0062101180 and M0062101600 worldwide. Healthcare providers should stop using the device immediately and follow manufacturer recall instructions.

Boston Scientific
The Encore
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Health & Personal Care
HIGH
FDA DEVICE

AVID Medical JACK421-04 ENT PACK Recalled for Sterility Risk (2025)

AVID Medical recalled 57 JACK421-04 ENT PACK convenience kits nationwide in Florida. The open header bag seals could compromise sterility. Consumers should stop using the device and follow manufacturer instructions for recall resolution.

AVID Medical
Potential for
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Health & Personal Care
HIGH
FDA DRUG

Hospira Epinephrine Injection Vials Recalled for Lack of Sterility Assurance (2025)

Hospira recalls 49,620 vials of Epinephrine Injection, distributed nationwide in the United States. The recall, active since August 4, 2025, targets vials with NDC 0409-4933-05 and case NDC 0409-4933-10. The hazard is lack of assurance of sterility. Health professionals should stop using the product and contact Pfizer or a healthcare provider for guidance.

Epinephrine
Lack of
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Recalled Baby Loren Children's Joy Loungewear
HIGH
CPSC

Baby Loren Recalls 4 Morning Loungewear Styles for Burn Risk (2025)

Baby Loren recalls four Morning children’s 100% cotton loungewear dresses in 2025 for fire safety violations. The recall involves dresses with neck labels listing October 2022 or October 2023 and batch numbers ending in 3465, 3585, 3599 or 3569. Consumers should stop using the dresses and contact Baby Loren for a full refund.

Baby Loren
The recalled
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Recalled KidKraft Farm to Table Play Kitchen
CRITICAL
CPSC

KidKraft Backyard Kids Farm to Table Play Kitchen Recall 2025 After Strangulation Hazard

Backyard Kids recalled KidKraft Farm to Table Play Kitchens in 2025 after one death was reported at multiple retailers. The hazard arises from hooks that hold toy accessories where clothing can snag during climbing or crawling through the back opening. Stop using the play kitchen immediately and contact Backyard Kids for free replacement hooks or repair.

KidKraft
If young
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Recalled Minecraft Light-Up Slap Ruler Bracelet, Model 718508MCR - Front
HIGH
CPSC

Innovative Designs Recalls Minecraft Light-Up Slap Ruler Bracelets (2025)

Innovative Designs recalled Minecraft Light-Up Slap Ruler Bracelets sold at retailers due to a button cell battery ingestion hazard. The recall covers models 718508MCR and 718075MCR. Consumers should stop using the recalled bracelets immediately and email disposal photos to info@innovativenyc.com to receive a full refund.

Innovative Designs
The battery
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Recalled Aiho Five-Drawer Dresser (front)
HIGH
CPSC

Aiho Five-Drawer Dresser Recalled for Tip-Over Hazard at Walmart in 2025

Aiho recalled its five-drawer dressers sold on Walmart.com after safety concerns over tip-over and entrapment hazards. The white dressers measure about 16 inches deep, 28 inches wide, and 37 inches tall. Model AP23-W is printed on the packaging. Consumers should stop using the dresser if it is not wall-anchored and contact Aiho for a full refund and disposal instructions.

Aiho
The recalled
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Example of child using the compression strap to stand on above-ground pool, illustrating the hazard involved
CRITICAL
CPSC

Bestway, Intex and Polygroup Recall 48-Inch+ Above-Ground Pools Over Drowning Hazard (2025)

Bestway, Intex and Polygroup recall 5 million above-ground pools taller than 48 inches after nine deaths. The recall covers pools whose model numbers are printed on the liner outside the pool. The hazard stems from a compression strap around the pool legs that can create a foothold for a child, enabling access to the water. Stop using the pools immediately and contact the respective brands for a维修

Bestway
The compression
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Health & Personal Care
HIGH
FDA DRUG

DermaSarra External Analgesic Recalled for Burkholderia Cepecia Contamination (DermaRite Industries)

DermaRite Industries recalled 249 bottles of DermaSarra External Analgesic on July 17, 2025 due to microbial contamination. The product, sold nationwide, carries NDC 61924-189-08 and Lot 40187.2 with an expiration date of February 2026. Consumers should stop using the product immediately and contact DermaRite for guidance.

DERMASARRA
Microbial Contamination
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