cpsc regulated Recalls

2,142 recalls tagged with “cpsc regulated”.

Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Syringe Recalled Globally Over Rotation Adaptor Risk (2026)

Medline Industries, LP recalled 149,439 NAMIC Angiographic Syringes worldwide, including the US and several international markets. The post-market signal shows a potential rotation adaptor unwinding during use, which can cause a loose or complete disconnect with the manifold. Health care providers and patients should stop using the devices and follow Medline's recall instructions.

Medline Industries, LP
Medline Industries,
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Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Syringes Recalled Globally for Rotating Adaptor Unwinding Risk (Class I)

Medline Industries recalled 2,630,369 NAMIC Angiographic Syringes worldwide after post-market surveillance found a potential risk that the syringe rotating adaptor could unwind during use, causing a loose connection or disconnection with the manifold. Healthcare providers must stop using the device and follow recall instructions. Contact Medline or a healthcare provider for guidance.

Medline Industries, LP
Medline Industries,
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Convenience Kits Recalled Worldwide Over Rotating Adaptor Unwinding

Medline Industries, LP recalls 20 kits worldwide after post-market surveillance found a risk the syringe rotating adaptor may unwind during use, causing a loose connection or full disconnection with the manifold. The recall affects three Medline SKUs and includes UDI details and lot numbers. Healthcare providers and patients should stop using the device immediately and follow Medline's recall plan

Medline Industries, LP
Medline Industries,
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Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic RA Syringe Recall Expands to 966 Kits Worldwide (2026)

Medline Industries, LP recalls 966 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers kits labeled DELIVERY PACK with SKUs DYNJ42892F and DYNJ42892G distributed worldwide, including the US and PR. The defect is a rotating adaptor that may unwind, creating a loose connection or disconnection between syringe and manifold. Stop using the device and use

Medline Industries, LP
Medline Industries,
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Health & Personal Care
HIGH
FDA DRUG

Macleods Pharma USA Recalls 1,315 Levothyroxine 150 mcg Tablets (2026)

Macleods Pharma USA, Inc. recalls 1,315 bottles of Levothyroxine Sodium Tablets USP 150 mcg distributed nationwide. The drug is subpotent, which may not provide the full therapeutic dose. Stop using and contact your healthcare provider or Macleods Pharma USA, Inc. for guidance.

LEVOTHYROXINE SODIUM
Subpotent Drug
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Pepsin Powder Recall 468 kg Over Salmonella Contamination (2026)

American Laboratories recalled 468 kg of Pepsin 1:3000 Powder distributed through 11 wholesale accounts in the United States and one in Australia. The powder is potentially contaminated with Salmonella and could cause illness if used. Consumers who purchased this product should not consume it and should contact American Laboratories by email for refund or replacement.

American Laboratories
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Recalls 370 kg Pepsin 1:10,000 Powder Over Salmonella Risk (2026)

American Laboratories recalled 370 kg of Pepsin 1:10,000 Powder sold through 11 wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one account in Australia after a potential Salmonella contamination. The product carries a possible Salmonella contamination risk. Consumers should not consume the product and should contact American Laboratories for refund or replacement via email.

American Laboratories
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Pepsin Full Strength Powder Recalled for Salmonella Contamination (400 kg, 202

American Laboratories recalled 400 kg of Pepsin Full Strength Powder sold to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one wholesale account in Australia after a recall cited potential Salmonella contamination. The product is Item #5000545 and packed in double poly-lined drums or boxes. Consumers should not consume this product and should contact American Laboratories,

American Laboratories
Potential Salmonella
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Recalled TheKiddoSpace LED Soccer Hover Ball
HIGH
CPSC

TheKiddoSpace Recalls LED Soccer Hover Balls Over Burn Risk

TheKiddoSpace recalled LED soccer hover balls on February 26, 2026, due to a burn hazard. The balls exceed the allowable surface temperature for batteries, posing serious injury risks. Consumers should stop using these toys immediately and seek a replacement.

TheKiddoSpace
The surface
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Recalled Zelbuck "Magnetism ball game" – box
HIGH
CPSC

Zelbuck Children's Chess Games Recalled Over Magnet Ingestion Risk

Zelbuck recalled children's chess games on February 26, 2026, due to a serious ingestion hazard. The games contain loose magnets that can lead to serious injury or death if swallowed. Consumers should stop using the games immediately and seek a full refund.

Zelbuck Children's Chess Games
The recalled
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Recalled window opening control device installed on 100 Series casement windows
MEDIUM
CPSC

Andersen Windows Recalls Control Devices Over Fall Hazards

Andersen Windows recalled window opening control devices on February 26, 2026. The recall affects devices sold individually or installed on 100 Series casement windows manufactured before November 19, 2025. These devices pose fall and serious injury hazards due to the potential for detachment.

Andersen Windows
The window
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Recalled Dupray Neat Steam Cleaner
HIGH
CPSC

Dupray Recalls Neat Steam Cleaners Over Burn Hazard Risk

Dupray USA recalled portable Neat Steam Cleaners on February 26, 2026, due to burn hazards. The model number is DUP020WNA, with batch codes from 0118-01 to 0425-05. Consumers should stop using the product immediately and follow safety instructions for a free replacement part.

Dupray USA
The steam
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Recalled Royal Oak Flame Saber Lighter
HIGH
CPSC

Royal Oak Recalls Lighters Over Serious Fire and Burn Hazards

Royal Oak Enterprises recalled flame saber lighters on February 26, 2026, due to serious fire and burn hazards. The lighters lack child-resistant mechanisms and violate labeling requirements. Consumers should stop using these lighters immediately and seek a refund.

Royal Oak Enterprises
The recalled
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Recalled TheKiddoSpace Toy - Peg Dolls in Cups
HIGH
CPSC

TheKiddoSpace Recalls Peg Doll Toys Due to Choking Hazard

TheKiddoSpace recalled peg doll toys on February 26, 2026, due to a choking hazard. The toys can block a child's airway, posing a risk of serious injury or death. Consumers should stop using the toys immediately and return them for a full refund.

TheKiddoSpace
The recalled
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Recalled Somgem Lightweight Tiny Pinky Pig Lighter
HIGH
CPSC

Somgem and Yomin Toilet Lighters Recalled for Fire Hazard

Somgem and Yomin recalled pig and toilet lighters on February 26, 2026. The lighters lack child-resistant features, posing serious burn risks. Consumers should stop using these products immediately and seek refunds.

Somgem Pig and Yomin Toilet Lighters
The recalled
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Tag Statistics

Total Recalls
2,142

Related Tags

electrical hazardchemical hazardinfant productadult productworkplaceplasticmetalimmediate actionstop use immediatelyreturn for refundfda regulatedreplacement available