Recall database

All Product Recalls

Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
Active recalls
4,434
Current page
139
Health & Personal Care
HIGH
FDA DEVICE

Zimmer Recalls Affixus Femoral Nails Over Fatigue Fracture Risk

Zimmer, Inc. recalled 23 Affixus Antegrade Femoral Nails on December 2, 2025. These implants may have an undersized distal diameter that could lead to fatigue fractures. Patients should stop using the device immediately and contact their healthcare provider.

Zimmer
Affected implants
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Health & Personal Care
HIGH
FDA DEVICE

Zimmer Recalls Affixus Femoral Nails Due to Fracture Risk

Zimmer, Inc. recalled 11 units of the Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may have an undersized distal diameter, posing a risk of fatigue fracture. This defect could cause adverse reactions requiring surgical intervention.

Zimmer
Affected implants
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Health & Personal Care
HIGH
FDA DEVICE

Zimmer Recalls Affixus Femoral Nails Due to Fracture Risk

Zimmer recalled 11 Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may fracture, leading to serious health risks. Patients should stop using the device immediately and follow manufacturer instructions.

Zimmer
Affected implants
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Health & Personal Care
HIGH
FDA DEVICE

Affixus Antegrade Femoral Nails Recalled Over Fracture Risk

Zimmer Inc. recalled 24 Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may have undersized distal diameters, leading to potential fractures. Users should stop using the product immediately and contact their healthcare provider.

Zimmer
Affected implants
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Health & Personal Care
HIGH
FDA DEVICE

Zimmer Recalls Affixus Femoral Nails Due to Fracture Risk

Zimmer Inc. recalled 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have undersized distal diameters, risking implant fatigue fractures. Consumers should stop using the device immediately and follow manufacturer instructions.

Zimmer
Affected implants
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Food & Beverages
HIGH
FDA FOOD

Fazt & Loud Energy Drink Recalled Over Caffeine Misprint

Fazt & Loud LLC recalled its Sour Gummy Bear energy drinks on December 2, 2025. The product contains 300 mg of caffeine instead of the labeled 150 mg. Consumers should stop using the product and seek a refund or replacement.

Fazt & Loud
Recall is
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