fabric Recalls

62 recalls tagged with “fabric”.

Recalled Bellabu Bear Children's Robe - Batman
HIGH
CPSC

Bellabu Bear Recalls Bamboo Sherpa Children's Robes for Burn Hazard (2025)

Bellabu Bear recalls its bamboo sherpa children's robes sold at Saks Fifth Avenue stores and online retailers from January 2024 through July 2025 for about $60. The robes do not meet mandatory flammability standards for children's sleepwear and pose a burn risk. Stop using the recalled robes and contact Bellabu Bear for a full refund or store credit.

Bellabu Bear
The recalled
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Recalled Persilux Zebra Blinds
HIGH
CPSC

Persilux Zebra Blinds Recalled for Strangulation Risk, Sold on Amazon

Persilux recalled zebra blinds sold on Amazon after safety hazards were found. The recall cites long operating cords that can cause strangulation and entanglement. The company offers a free repair kit and instructions to remove cords. Consumers should stop using the product immediately and contact Persilux for remedy information.

Persilux
The recalled
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Vehicles & Parts
HIGH
NHTSA

Audi S5 Front Seat Belt Retractor Recall Affects 2025 VW Group Vehicles

Audi and Volkswagen Group of America recall 2025 GTI, Golf R, Audi A5, A6 Sportback E-Tron, S5, S6 Sportback E-Tron, 2026 Q4 Sportback E-Tron and Q4 E-Tron vehicles. The torsion bar in the front seat belt retractors may be damaged during production. Dealers will replace one or both front seat belts at no charge. VIN lookups begin Sept 26, 2025 and owner letters go out Nov 21, 2025.

Audi
In a
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Health & Personal Care
HIGH
FDA DEVICE

BD BACTEC Blood Culture System Recall 1,086 Units Worldwide Over Unauthorized Access Risk (2025)

BD recalled 1,086 BD BACTEC Blood Culture System units worldwide after unauthorized access to product service credentials. The breach could compromise confidentiality, integrity and availability of affected devices and data. Hospitals and healthcare providers should stop using the device immediately and follow BD’s recall instructions.

BD
Product service
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Recalled In My Jammers Button Up Flare Set – Victoria print
HIGH
CPSC

In My Jammers Recalls Button Flare Pajama Sets for Burn Hazard in 2025

In My Jammers recalls children's button-up flare pajama sets sold online after the company violated mandatory flammability standards. The recall, active as of Sept. 11, 2025, involves sets in multiple prints and sizes. Parents should stop using them and seek a full refund or store credit.

In My Jammers
The recalled
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Recalled URMYWO Baby Lounger – Grey Feather
HIGH
CPSC

URMYWO Baby Loungers Recalled for Suffocation and Fall Hazards; 2025 Recall Active

URMYWO recalled its baby loungers on 2025-09-04 after reports of suffocation and fall hazards. The recall targets URMYWO loungers style grey feather sold via Amazon by Pomona. The devices fail to meet infant sleep standards due to short side walls and excessive pad thickness. Consumers should stop using the loungers and request a full refund.

URMYWO
The baby
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Health & Personal Care
HIGH
FDA DEVICE

ConvaTec DuoDERM Extra Thin Dressings Recalled in 2025 for Foreign Matter

ConvaTec recalled 80,980 DuoDERM Extra Thin wound dressings distributed nationwide in the United States. The dressings may contain foreign matter, which could compromise wound care. Healthcare providers and patients should stop using the dressings and follow recall instructions.

ConvaTec
Wound dressing
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Recalled Lulive 12-Drawer Dresser (front)
HIGH
CPSC

Lulive 12-Drawer Dressers Recalled for Tip-Over Risk in 2025

Lulive recalled 12-drawer dressers sold on Amazon after identifying a risk of serious injury or death from tip-over and entrapment. The dressers are white with a metal frame, a wooden top, 12 collapsing fabric drawers, four side pockets and two hooks. They measure about 12 inches by 39 inches by 45 inches and weigh 30 pounds. Consumers should stop using unanchored dressers immediately and contactL

Lulive
The recalled
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Food & Beverages
HIGH
FDA FOOD

Baker's Authority Recalls 78 Units of Three Seed Mix for Sesame Allergen (2025)

Baker's Authority LLC recalls 78 units of Three Seed Mix, 5 lb bags, distributed to multiple states. The recall follows labeling errors that fail to list sesame as an ingredient. Consumers who purchased this product should not consume it and should email Baker's Authority LLC for refund or replacement information.

Baker's Authority
Product label
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Food & Beverages
HIGH
FDA FOOD

H & N Group Frozen Shrimp Recalled for Cs-137 Contamination (2025)

H & N Group recalled 17,214 cases of frozen shrimp distributed to East Coast retailers after potential Cs-137 contamination. The product was manufactured under insanitary conditions. Consumers should not eat this product and should contact H & N Group for refund or replacement by telephone.

H & N Group
Product manufactured
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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 WLIVE Fabric 15-Drawer Dresser in Rustic Brown
HIGH
CPSC

WLIVE Fabric 15-Drawer Dressers Recalled for Tip-Over Risk Sold on Amazon (2025)

WLIVE recalled its Fabric 15-Drawer Dressers sold on Amazon after reports of tip-over and entrapment hazards. The dressers can tip when not anchored to a wall, posing serious injury or death risk to children and violating the STURDY standard. Consumers should stop using unanchored dressers and contact WLIVE for a full refund.

WLIVE
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

BioFire Defense FilmArray NGDS Warrior Panel NGDS-ASY-0007 Recall 130 Kits in 2025

BioFire Defense recalled 130 FilmArray NGDS Warrior Panel NGDS-ASY-0007 kits distributed nationwide in the United States. The recall cites an increased risk of internal control failures when testing positive blood cultures. Clinicians should stop using the device immediately and follow recall instructions provided by BioFire Defense. Notification is by letter to affected facilities.

BioFire Defense
FilmArray NGDS
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