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. 2,604 recalls have been distributed to Indiana in the last 12 months.
Showing 18381–18400 of 53,528 recalls
Recalled Item: MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere iCup Drug Detection (AMT Item Number/ AMT Description): I-DXA-10/...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fastect¿ II Drug Screen Dipstick Test Single Drug Detection (AMT Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Check 1 Panel Drug Cup: (THC) Recalled by Ameditech Inc Due to Various...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLIA Waived Rapid Drug Test (AMT Item Number/ AMT Description): Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Goldenseal Root Powder Organic Recalled by Maison Terre, LLC Due to...
The Issue: Microbial Contamination of Non-Sterile Products: FDA laboratory analysis...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tranexamic Acid Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amiodarone Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Speed Stitch Needle Cassette Recalled by ArthroCare Corporation Due to Due...
The Issue: Due to a supplier error where a portion of the raw material was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...
The Issue: Chemical Contamination: FDA analysis found the product contains methanol,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...
The Issue: CGMP Deviations: All other lots are being recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump Recalled...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine HCl Injection Recalled by Hikma Pharmaceuticals USA Inc. Due...
The Issue: Sub-potent Drug: Out-of-Specification assay results found at 3 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dual Mobility Vivacit-E Bearing Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The outer package is labeled as a Size C 38 mm, however, the implant inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...
The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Innovations ROM Plus Collection Kit IFU: ROM Plus Rupture Recalled...
The Issue: Possible false negative or false positive results. The incorrect sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Decontamination System (CCDS) Compatible N95 respirators -...
The Issue: Masks processed at one site were not maintained at levels of condensation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.