infant product Recalls

794 recalls tagged with “infant product”.

Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC RA Syringe Recall: 108 Units Worldwide for Unwinding Adaptor (High Risk)

Medline Industries, LP recalls 108 NAMIC Angiographic Rotating Adaptor Syringes sold worldwide, including the United States, PR and several international markets. The rotating adaptor may unwind during use, creating a loose connection or disconnection with the manifold. Healthcare providers must stop using the device and follow recall instructions.

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

Medline NAMIC Angiographic Adaptor Syringe Recall Expands Worldwide in 240 Kits (Class I)

Medline Industries, LP recalled 240 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers worldwide distribution including the US, Puerto Rico, and multiple international markets. The potential issue is the adaptor unwinding during use, risking a loose connection or disconnection with the manifold.

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

Medline NAMIC Angiographic Syringe Recall for 2,154 Kits Worldwide

Medline Industries, LP recalls 2,154 medical convenience kits worldwide after post-market surveillance found a risk that the NAMIC Angiographic Rotating Adaptor may unwind. A loose connection or disconnection between the syringe and manifold could occur. Stop using immediately and follow manufacturer recall instructions.

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

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in 82 Kits Worldwide

Medline Industries, LP recalled 82 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers two Medline SKUs and spans worldwide distribution, including the US, Puerto Rico and several countries. The defect is a rotating adaptor that may unwind, causing loose connections or disconnections between syringe and manifold.

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

Medline NAMIC Angiographic Syringe Recall for 1.75 Million Kits Over Adaptor Unwinding Risk (2026)

Medline Industries, LP recalls 1,752,096 NAMIC Angiographic Syringe kits worldwide, including the US and Canada. The recall stems from a post-market signal about the rotating adaptor unwinding during use. This may cause a loose connection or disconnection between the syringe and manifold. Health care providers and patients should stop using the devices and follow recall instructions.

Medline Industries, LP
Medline Industries,
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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 Rotating Adaptor Syringes Recalled in 2,980 Kits Worldwide

Medline Industries, LP recalls 2,980 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans the United States, Puerto Rico and multiple international countries. The rotatable adaptor may unwind during use, risking a loose connection or disconnection between syringe and manifold. Patients and healthcare providers should stop using the device and followMed

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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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 Bicystar High Chair - model TB-HC6900
HIGH
CPSC

Bicystar High Chairs Recalled Due to Fall and Entrapment Risks

Bicystar recalled children's high chairs on February 26, 2026, due to serious fall and entrapment hazards. The affected high chairs lack required crotch restraints, putting children at risk. Consumers should stop using these chairs immediately and seek a refund.

Bicystar High Chairs
The high
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Recalled Babysense Max View 5.5" Baby Monitor display/parent unit
HIGH
CPSC

Babysense Max View Baby Monitors Recalled Due to Fire Hazard

Hisense recalled Babysense Max View baby monitors on February 26 after reports of overheating display units. The recall affects model VBM55, with incidents of sparking during charging. Consumers should stop using the device immediately and contact Hisense for a replacement.

Hisense Ltd., of Israel
The display
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Tag Statistics

Total Recalls
794

Related Tags

fire hazardelectrical hazardchemical hazardsuffocation risktoddler productadult productelderly productimmediate actionstop use immediatelyreturn for refundreplacement availablefederal law violation