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 44801–44820 of 53,528 recalls
Recalled Item: PROMETHAZINE HYDROCHLORIDE Tablets Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: Presence of Foreign Tablets: Presence of atenolol 25 mg tablet mixed into...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Devon Supine Recalled by Covidien LLC Due to Straps may separate from the...
The Issue: Straps may separate from the foam pad.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach Pneumatic and Electric Motor Systems. Intended for cutting and...
The Issue: Several attachments and handpieces failed to meet the expected sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACROLYTE Premie Dispersive Electrode Recalled by ConMed Corporation Due to...
The Issue: ConMed Corporation has received complaints regarding sparking, no output and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Post Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Rod Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luxurian. These include all products labeled as UltraSlim Recalled by...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraslim. These include all products labeled as UltraSlim Recalled by...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Photonica Light Modulator. These include all products labeled as UltraSlim...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS System Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a potential risk when using LANTIS OIS System client software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visitec Anterior Chamber Cannula Recalled by Beaver-Visitec International...
The Issue: Contains a sharp tip needle when the product should contain a blunt tip cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFRICAN BLACK ANT Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MOJO RISEN Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Black Ant Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hemo-Stat Solution Recalled by Axcentria Pharmaceuticals, LLC Due to...
The Issue: Marketed without an Approved NDA/ANDA; product is being manufactured and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Good Herbs Recalled by Good Herbs, Inc. Due to Products not manufactured...
The Issue: Products not manufactured under GMP's
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Good Herbs Recalled by Good Herbs, Inc. Due to Products not manufactured...
The Issue: Products not manufactured under GMP's
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Good Herbs Recalled by Good Herbs, Inc. Due to Products not manufactured...
The Issue: Products not manufactured under GMP's
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Good Herbs Recalled by Good Herbs, Inc. Due to Products not manufactured...
The Issue: Products not manufactured under GMP's
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Good Herbs Recalled by Good Herbs, Inc. Due to Products not manufactured...
The Issue: Products not manufactured under GMP's
Recommended Action: Do not consume. Return to store for a refund or discard.