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. 2,560 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,560 in last 12 months

Showing 2500125020 of 53,528 recalls

FoodOctober 15, 2018· Request Foods Incorporated

Recalled Item: Kashi Recalled by Request Foods Incorporated Due to Potential Salmonella...

The Issue: The firm was notified by their supplier that ingredients used in their...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 15, 2018· Request Foods Incorporated

Recalled Item: Beecher's Enchilada Bowl Blanco 9oz. Frozen 8 Recalled by Request Foods...

The Issue: The firm was notified by their supplier that ingredients used in their...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2018· Baxter Healthcare Corporation

Recalled Item: Metoprolol Tartrate Injection Recalled by Baxter Healthcare Corporation Due...

The Issue: Failed pH Specifications: Upward shift in the pH of the solution within the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2018· Heritage Pharmaceuticals, Inc.

Recalled Item: Cidofovir injection 375 mg/mL (75 mg/mL) vial Injection Recalled by Heritage...

The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2018· Zero Xtreme USA

Recalled Item: Zero Xtreme Dietary Supplement 30-count capsules. By:Zero Xtreme Registro...

The Issue: Marketed Without an Approved NDA/ANDA: Undeclared Sibutramine

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 12, 2018· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...

The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Compress Devices and Instruments: Item Number/Item Description 178350...

The Issue: Correction to update the surgical technique for the Compress System. To make...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Total T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...

The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Atrium Medical Corporation

Recalled Item: Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE Recalled by Atrium Medical...

The Issue: This recall has been initiated in response to a seal defect found in certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2018· St. Jude Medical, Inc.

Recalled Item: St. Jude Medical InfinityTM DBS System 8CH Directional Lead Recalled by St....

The Issue: The most proximal unsegmented electrode of the Deep Brain Stimulation leads,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed that Dimension Vista Lactate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 11, 2018· Lannett Company, Inc.

Recalled Item: HydrOXYzine HYDROCHLORIDE SYRUP (HydrOXYzine Hydrochloride Oral Solution...

The Issue: CGMP Deviations: cleaning procedures during manufacturing caused out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 11, 2018· FOODSTIRS

Recalled Item: Foodstirs Modern Baking Recalled by FOODSTIRS Due to Individual pouches of...

The Issue: Individual pouches of Organic Minute Mug Cake Mix Celebration Confetti...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 11, 2018· Feel Good Foods Inc

Recalled Item: feel good foods VEGETABLE FRIED RICE NET WT 9 OZ (255G) Recalled by Feel...

The Issue: Product contains undeclared egg.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 10, 2018· Quest Nutrition, LLC

Recalled Item: Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# - Recalled by Quest...

The Issue: Undeclared allergen; tree nut (almonds)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 10, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Naera Hospital Bassinet Recalled by Stryker Medical Division of Stryker...

The Issue: It was identified that the volume of air inside the mattress may expand in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: A problem has been detected in the Philips IntelliVue MX4O that, if it were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Zimmer Biomet, Inc.

Recalled Item: Comprehensive Mini Stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet is conducting a lot specific medical device recall for two...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Porous Stem Recalled by Zimmer Biomet, Inc....

The Issue: Zimmer Biomet is conducting a lot specific medical device recall for two...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart FR3 Defibrillator Recalled by Philips Electronics North...

The Issue: Automated external defibrillators may not fully meet IPx5 water ingress...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing