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. 2,535 recalls have been distributed to Indiana in the last 12 months.
Showing 32141–32160 of 53,528 recalls
Recalled Item: Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm) Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Item Code: 91650 The sterile eye Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Item Code: 03201 The sterile eye Recalled by...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Eye Pad Oval Recalled by Covidien LLC Due to Product...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kerlix Super Sponge Saline Dressing Recalled by Covidien LLC Due to...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Curity Sodium Chloride Dressing Recalled by Covidien LLC Due to...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Intelligent Lab System and Dimension Vista 1500 Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed that in isolated cases when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panta Nail Recalled by Integra LifeSciences Corp. Due to Voluntary...
The Issue: Voluntary recall/Removal of Panta and Panta XI Nails because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desonide Ointment Recalled by Fougera Pharmaceuticals Inc. Due to Labeling:...
The Issue: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: Ortho Kinematics notified customers that errors were contained in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eCare Coordinator Product Usage: is software intended for use in Recalled by...
The Issue: eCareCoordinator (eCC) is intended for use in data aggregation, patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Hyaluronic 1000 Recalled by Signature Club A Ltd Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: odor complaint of product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Parmesan Truffle Salt. The product is packaged in glass taster Recalled by...
The Issue: Parmigiano Reggiano (Parmesan) cheese is declared, but milk is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cobas 8100 bi-directional (BRF) module with Software Version 02-xx Recalled...
The Issue: "Roche Diagnostics Corp. initiated a voluntary correction because a rack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas 8100 uni-directional (BRF) module with Software Version 02-xx Recalled...
The Issue: Roche Diagnostics Corp. initiated a voluntary correction because a rack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by G & W Laboratories,...
The Issue: CGMP Deviations: an expired active ingredient was used in the manufacture of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Por fullct fem st 17x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 14mmdx48cm left Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx38cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.