choking hazard Recalls

233 recalls tagged with “choking hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalling 10 GEM Premier 5000 PAK Cartridges for PCSND Error During Warm‑

Instrumentation Laboratory recalled 10 GEM Premier 5000 PAK cartridges sold worldwide after reports of increased PCSND errors during warm‑up. The issue can cause GEM PAK ejections and delays in results. Clinicians and labs should follow the manufacturer’s recall instructions and seek guidance from their healthcare provider.

Instrumentation Laboratory
Confirmed customer
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Food & Beverages
HIGH
FDA FOOD

Frederik's by Meijer Focaccia Bread Recalled for Metal Fragments (2026)

Frederik's by Meijer Slow-Roasted Tomato & Parmesan Focaccia Bread recalled after metal fragments were found in 23,459 cases. The recalls spans Frederik's by Meijer, Fresh & Simple, HT Traders and Trader Joe's focaccia products. The metal fragments were traced to roasted tomatoes from an ingredient supplier. Stop using the product and contact the supplier for refunds or replacements.

Bakkavor
Metal fragments
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Recalled Greatale Self-Feeding Pillow
HIGH
CPSC

Greatale Recalls Self-Feeding Pillows Due to Suffocation Risk

Greatale recalled self-feeding pillows on January 15, 2026, due to a serious risk of aspiration and suffocation in infants. The pillows can hold a bottle at an unsafe angle, preventing infants from pulling away. Consumers must stop using the pillows immediately and return them for a full refund.

Greatale
The recalled
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Recalled Kori Gey Water Elf Toy Kit
HIGH
CPSC

Kori Gey Water Toy Kits Recalled Over Battery Ingestion Risk

Kori Gey recalled water elf toy kits on January 8, 2026, due to a severe risk of battery ingestion. The toy kits can expose children to dangerous button cell batteries. Consumers should stop using the kits immediately and seek a refund.

Kori Gey Water Toy Kits
The recalled
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Recalled Multifunction Pounding Game Packaging
HIGH
CPSC

Lterfear Pounding Game Recalled Due to Magnet Ingestion Risk

Lterfear recalled the Multifunction Pounding Game model D888 on January 8, 2026. The toy poses a serious ingestion hazard due to high-powered magnets that can detach. Consumers should stop using the toy immediately and seek a refund.

Pounding Toys
The recalled
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Food & Beverages
HIGH
FDA FOOD

Karison Foods Recalls Punjabi Pinni Over Undeclared Milk Hazard

Karison Foods & Snacks Inc. recalled 3,120 units of Punjabi Pinni on January 6, 2026, due to undeclared milk. Consumers with milk allergies risk serious health issues. The product was distributed in New York, New Jersey, and Virginia.

Karison Foods & Snacks
Product contains
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Health & Personal Care
HIGH
FDA DEVICE

Raz Design Raz-AT Mobile Shower Commode Chair Recall for 66 Units Over Bracket Engagement Hazard (Z-

Raz Design Inc recalled 66 Raz Mobile Shower Commode Chairs nationwide, citing a modification that may allow the seat to detach if outside rear brackets are not properly engaged. The recall covers multiple catalog numbers and serial ranges. Patients and healthcare providers should stop using the device immediately and contact Raz Design for instructions.

Raz Design
Due to
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Health & Personal Care
HIGH
FDA DRUG

Carmex Lip Balm Recalled by Gold Star Distribution for 12-Count Jars and Tubes (2026)

Gold Star Distribution Inc. is recalling Carmex lip balm in 12-count jars and 12-count tubes distributed nationwide in the United States. The recall cites CGMP deviations and insanitary conditions at the distribution center, including rodent exposure. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution for guidance.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Philips North America Issues Recall for Patient Information Center Software

Philips North America recalled 146 units of Patient Information Center software on December 22, 2025. A software patch modifies Mobile Event Notification filter settings without notifying users. The recall affects units distributed worldwide, including 41 in the U.S.

Philips North America
A recent
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Recalled Meaicezli Play Purse Set Packaging
HIGH
CPSC

Meaicezli Play Purse Sets Recalled Over Battery Ingestion Risk

Meaicezli recalled Play Purse Sets on December 18, 2025, due to a risk of serious injury from battery ingestion. The toys contain button cell and lithium coin batteries accessible to children. Consumers must stop using the products and return them for a full refund.

Meaicezli
The children's
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Recalled TopHomer Pool Drain Cover
MEDIUM
CPSC

TopHomer Pool Drain Covers Recalled Over Drowning Hazards

TopHomer recalled pool drain covers on December 18, 2025, due to serious entrapment and drowning hazards. The recall affects 8-inch drain covers sold on Amazon. Consumers should immediately stop using the products and seek refunds.

TopHomer Pool Drain Covers
The recalled
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Food & Beverages
HIGH
FDA FOOD

Prima Vera Nueva Recalls Tamales Due to Listeria Risk

Prima Vera Nueva recalled 30,327 packages of Butternut Squash Tamales on December 12, 2025. The product poses a high risk of contamination with Listeria monocytogenes. Consumers should not consume these tamales and should seek a refund or replacement.

Prima Vera Nueva
Potential contamination
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Recalled Uuoeebb Infant Walker in gray
HIGH
CPSC

BaoD Recalls Uuoeebb Infant Walkers Sold on Amazon for Fall and Entrapment Hazards (2025)

BaoD recalled Uuoeebb Infant Walkers sold on Amazon after safety hazards were identified. The walker can fit through a standard doorway and does not stop at a step edge, creating a fall hazard. The leg openings can allow a child to slip down until the head becomes entrapped. Consumers should stop using the recalled walker immediately and contact BaoD for a full refund.

Uuoeebb
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Intuitive Surgical da Vinci S/Si Monopolar Curved Scissors Recall for 86,904 Units Worldwide (2025)

Intuitive Surgical recalled 86,904 da Vinci S and Si Monopolar Curved Scissors instruments sold worldwide to hospitals and surgical centers. The recall cites increased complaints of broken or frayed grip cables on reusable instruments. Healthcare facilities should stop using the device immediately and follow the manufacturer’s recall instructions.

Intuitive Surgical
Due to
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