Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,781 recalls have been distributed to Indiana in the last 12 months.
Showing 48861–48880 of 53,528 recalls
Recalled Item: 00597001303 Femur CR PRC FEM COMP SIZE CML Rx Recalled by Zimmer, Inc. Due...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597206126 Patella ALL POLY PAT COMP MICRO 26DIA Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597001131 Femur CR PRC SURF HDN FEM CO-NID AML Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Infusor SV and LV Elastomeric Infusion Devices. Indicated...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Multiday lnfusor Recalled by Baxter Healthcare Corp. Due to Due...
The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Basal/Bolus Infusor. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VECURONIUM Bromide for Injection Recalled by Sagent Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: product was not manufactured under current good...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Excedrin Extra Strength (Acetaminophen 250 mg Recalled by Novartis Consumer...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Parsel Plus ( US product: Excedrin Tension Headache) (Acetaminophen 500...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Excedrin Migraine (Acetaminophen 250 mg Recalled by Novartis Consumer Health...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The product has the potential for solution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: No Doz Recalled by Novartis Consumer Health Due to Defective container:...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD BBL Vancomycin Screen Agar Recalled by Becton Dickinson & Co. Due to...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Schaedler K-V Agar with 5% Sheep Blood Recalled by Becton Dickinson &...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL BBE // CDC Anaerobe Laked Sheep Blood Agar with KV Recalled by Becton...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Campylobacter CSM Agar (Charcoal-Based Selective Medium) Recalled by...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AOA Mini RPE Screw Assembly Recalled by Sybron Dental Specialties Due to The...
The Issue: The firm initiated the recall of AOA Mini RPE Screw Assembly, because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoGastric Solutions EsophyX2 Device with Serosa Fastener and Accessories....
The Issue: Endogastric Solutions, Inc. has received a limited number of reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.