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. 2,547 recalls have been distributed to Indiana in the last 12 months.
Showing 29961–29980 of 53,528 recalls
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Latanoprost PF Solution Recalled by ImprimisRx CA, Inc., dba ImprimisRx Due...
The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curcumin Emulsion 10mg/ml Injection Recalled by ImprimisRx CA, Inc., dba...
The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic...
The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol-Latanoprost PF Solution (0.5-0.005)% Recalled by ImprimisRx CA,...
The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Extended-Release Tablets USP Recalled by Lupin Pharmaceuticals...
The Issue: Failed Dissolution Specifications: out of specification observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUELICIN (Succinylcholine Chloride) Injection Recalled by Advanced Pharma...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.