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. 1,129 recalls have been distributed to Indiana in the last 12 months.
Showing 10121–10140 of 53,528 recalls
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcitonin Salmon Nasal Spray Recalled by Endo Pharmaceuticals, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications and Subpotent Drug: High Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobazam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Ophthalmic Solution 0.15% Recalled by Apotex Corp. Due...
The Issue: Lack of sterility assurance: Cracks have developed in some of the units caps...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium Recalled by B. Braun Medical Inc Due to Subpotent Drug: low...
The Issue: Subpotent Drug: low Anti-Factor IIa potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DG Health brand Sugar Free Daily Fiber in 10 oz. Recalled by Dollar General...
The Issue: Product is missing warning declaration that it contains phenylalanine.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Color Cuff Single Port Recalled by Stryker Sustainability Solutions Due to...
The Issue: Increased incidence of disposable tourniquet cuffs "not able to achieve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Step Bladeless Trocars Recalled by Covidien, LP Due to Medtronic was made...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Scro Zero Ang 20cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan NB Infra Zero Ang 16cm Recalled by Coloplast Manufacturing US, LLC Due...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Pump Recalled by Coloplast Manufacturing US, LLC Due to A...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Scrot Zero 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Scrotal 18 Cm Recalled by Coloplast Manufacturing US, LLC Due to...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Pump Assembly Recalled by Coloplast Manufacturing US, LLC Due to A...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Infr Zero 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mild Chromic Gut Absorbable Sutures Recalled by Covidien, LP Due to...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Scrotal 22 Cm Recalled by Coloplast Manufacturing US, LLC Due to...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Infr Zero Ang 22cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.