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. 963 recalls have been distributed to Indiana in the last 12 months.
Showing 47181–47200 of 53,528 recalls
Recalled Item: Self-Rising White Cornmeal Mix sold under the Aunt Jemima brand Recalled by...
The Issue: Some Aunt Jemima and Quaker brand Self-Rising Corn Meal Mix, Buttermilk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: White quick grits and grits packaged in a paper bag Recalled by Quaker Foods...
The Issue: Some Aunt Jemima and Quaker brand Self-Rising Corn Meal Mix, Buttermilk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Azure Anterior Cervical Plate System Recalled by Orthofix, Inc Due to There...
The Issue: There is a possibility that the locking mechanism of the Azure Anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS Urinalysis Control Level 1 Recalled by Thermofisher Scientive Due to Via...
The Issue: Via one (1) consumer complaint and in-house testing has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia E is a multi-purpose SPECT system ideal for hospitals Recalled by...
The Issue: Reports of loose bolts in the detector support structure of Symbia and E.CAM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott i-STAT PT/INR cartridges Abbott Point of Care Inc. Recalled by Abbott...
The Issue: Abbott Point of Care Inc (APOC) has determined that i-Stat PT/INR cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam line of gamma camera systems Used to detect or Recalled by Siemens...
The Issue: Reports of loose bolts in the detector support structure of Symbia and e.cam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Nephros SafeShower FH - 15 filters per box Recalled by Nephros Inc Due to...
The Issue: Promotional materials for non-medical water filtration products were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 3T MRI System Recalled by Toshiba American Medical Systems Inc Due to...
The Issue: Toshiba America Medical Systems, Inc. is recalling due to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...
The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nephros Dual Stage Ultra Filter (DSU) Brochure Document 60-3003 Revisions: 0...
The Issue: Promotional materials for non-medical water filtration products were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Disposable Recalled by Integra LifeSciences Corp. d.b.a. Integra...
The Issue: Integra LifeSciences Corporation is recalling certain lots of Integra Kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nephros SafeSpout Manufacturer: Nephros Inc. 41 Grand Avenue Recalled by...
The Issue: Promotional materials for non-medical water filtration products were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dura Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...
The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acyclovir Oral Suspension Recalled by Hi-Tech Pharmacal Co., Inc. Due to...
The Issue: Failed Stability Specification; product viscosity and or pH are below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACCU-CHEK Aviva Combo Blood Glucose Meter (as a part of Recalled by Roche...
The Issue: There is a software synchronization issue with the ACCU-CHEK Combo system....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) List number 126970465 labeled in part: 12697-65 LifeShield Recalled...
The Issue: Several lots of the LifeShield Latex-Free HEMA Y-Type Blood Set IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery NMCT 670 Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Security (TM) Enclosed Carpal Tunnel System Blade ( Recalled by Biomet, Inc....
The Issue: Security Blades were manufactured oversized and potentially won't advance or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Civco Belly Board MRI Recalled by Civco Medical Instruments Inc Due to...
The Issue: Scales adhered to the product may be misaligned from the zero such that one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.