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. 2,768 recalls have been distributed to Indiana in the last 12 months.
Showing 3361–3380 of 53,528 recalls
Recalled Item: ASIN B084PZ7K98 Recalled by Amazon Retail LLC Due to Undeclared Egg
The Issue: Undeclared egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid...
The Issue: Devices were distributed in the U.S. market without obtaining the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device...
The Issue: Devices were distributed in the U.S. market without obtaining the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Module The BD Alaris System Recalled by CareFusion 303, Inc....
The Issue: Due to User Manual/Direction for Use incorrectly instructing user to leave...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedFlex 2.0 Bio-ID Spare Parts by CareFusion 303, Inc. Due to Due...
The Issue: Due to fingerprint scanner failing resulting in the scanner heating up.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned Recalled by La Fiesta...
The Issue: Firm distributed a Seasoned Bread Crumb product with undeclared allergen...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: La Fiesta PAN RAYADO Bread Crumbs Recalled by La Fiesta Food Products Due to...
The Issue: Firm distributed a Bread Crumb product with undeclared allergen (Sesame) not...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...
The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Provepharm Inc. Due to Presence of...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...
The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...
The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP Recalled by AvKARE Due to Out of Specification for...
The Issue: Out of Specification for Dissolution
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate Recalled by...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 6H LT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.