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. 1,101 recalls have been distributed to Indiana in the last 12 months.
Showing 13281–13300 of 53,528 recalls
Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinici X da Vinci Xi Sureform 45 Recalled by Intuitive Surgical, Inc. Due...
The Issue: As a result of complaint data review, it identified tissue pushout events...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glycopyrrolate Tablets Recalled by Aurolife Pharma, LLC Due to Presence of...
The Issue: Presence of Foreign Substance: Complaint for pieces of glass discovered in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvstatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LetsGetChecked Blood Sample Collection kit-In vitro diagnostic medical...
The Issue: Users received sample collection kits that were assigned to another user....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Separation Technology Creamatocrit Plus Recalled by Stanbio Laboratory, LP...
The Issue: The device was being marketed as an IVD without a 510(k). Therefore,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.