immediate action Recalls
2,756 recalls tagged with “immediate action”.
Zimmer Recalls Affixus Antegrade Femoral Nails Due to Fatigue Fracture Risk
Zimmer recalled 23 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized distal diameter, leading to potential fatigue fractures. Health risks include pain, tissue damage, and the need for surgical intervention.
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 Recalls Affixus Antegrade Femoral Nails Over Fracture Risk
Zimmer issued a recall for 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized diameter, risking fatigue fractures. This defect could lead to severe health complications for patients.
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.
Affixus Antegrade Femoral Nailing System Recalled Over Fracture Risk
Microbiologics Recalls LYFO DISK Due to Testing Failure Risk
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
Volkswagen Recalls 2025 Atlas and Atlas Cross Sport for Transmission Issue
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2025 Atlas and Atlas Cross Sport vehicles. The transmission may have been manufactured incorrectly, which can result in a loss of drive power.
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 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 Recalls Affixus Antegrade Femoral Nails Due to Fracture Risk
Affixus Antegrade Femoral Nailing System Recalled Over Fatigue Risk
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.
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.