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. 2,577 recalls have been distributed to Indiana in the last 12 months.
Showing 21781–21800 of 53,528 recalls
Recalled Item: AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg Recalled...
The Issue: Failed Stability Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C....
The Issue: Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamivudine Tablets Recalled by American Health Packaging Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Karl Storz NEURO-FIBERSCOPE Recalled by Karl Storz Endoscopy Due to During a...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE Recalled by Karl Storz Endoscopy...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz Recalled by Karl Storz Endoscopy Due to During a complaint...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix Recalled by...
The Issue: Product tested positive for gluten but is labeled as Gluten free
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PediaSmart Organic Soy Vanilla Beverage Mix Recalled by Natures One Inc Due...
The Issue: Undeclared milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Control Panel 60-02-15: LivaNova SCP Pump Control Panel. Recalled by...
The Issue: The SCP control Panel rotary knob used to control rotary speed of the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Control Panel 60-02-50: LivaNova SCP Pump Control Panel Recalled by LivaNova...
The Issue: The SCP control Panel rotary knob used to control rotary speed of the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...
The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entropic Labs SARM RAD-140 Recalled by Tuscano and Delucia Group (DBA...
The Issue: Marketed Without An Approved NDA/ANDA: product contains Selective Androgen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fexofenadine hydrochloride tablets USP Recalled by Aurolife Pharma, LLC Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Fex (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.