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. 1,097 recalls have been distributed to Indiana in the last 12 months.
Showing 15021–15040 of 53,528 recalls
Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methocarbamol 500mg Tablet Recalled by Bryant Ranch Prepack, Inc. dba BRP...
The Issue: Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: CGMP Deviations: Lots recalled because they were manufactured at the same...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147...
The Issue: Due to an increased risk of false positive Acinetobacter calcoaceticus-...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affected components are limited to the Monoprice charging cable (Product...
The Issue: Warning Added: Using damaged cables or chargers, or charging when moisture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant 3.5x10 Recalled by Jjgc Industria E Comercio De...
The Issue: 3.5x11.5mm implants were mislabeled as 3.5x10mm implants. In borderline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transseptal Needle with Catheter. RPN TSN-17-75.0-ENDRYS. GPN G19261....
The Issue: Transseptal needles may contain rust on the interior and/or exterior of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Xstar Crescent Knife Recalled by Beaver Visitec International, Inc....
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transseptal Needle Recalled by Cook Inc. Due to Transseptal needles may...
The Issue: Transseptal needles may contain rust on the interior and/or exterior of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-AMO Germany GmbH Katarakt-set - Dr. Wagner: CustomEyes...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.