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. 2,455 recalls have been distributed to Indiana in the last 12 months.
Showing 47561–47580 of 53,528 recalls
Recalled Item: HGE Healthcare Patient Monitor B30 Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 ultrasound system. GE Vivid E9 is a Recalled by GE Healthcare,...
The Issue: GE became aware of a potential safety issue due to a system slow down and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-Ray System Recalled by Philips Medical...
The Issue: If the couch, with the footrest extension attached, is positioned where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude Medical...
The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules Recalled by Pure...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules Recalled...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules Recalled by Pure...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi BTrim MAX Dietary Supplement capsules Recalled by Pure Edge...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi INSANE Bee Pollen Dietary Supplement Capsules Recalled by Pure Edge...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi INSANE AMP'D Dietary Supplement capsules Recalled by Pure Edge...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Total Enzyme Recalled by Nutrition Center, Inc. dba Nutri-West Due to...
The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Total Probiotics Recalled by Nutrition Center, Inc. dba Nutri-West Due to...
The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Drill (Fluted-Hard Bone) Recalled by Cayenne Medical Inc. Due to A review of...
The Issue: A review of complaints identified a trend for drills breaking.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariAx Compression Plating System Recalled by Stryker Howmedica Osteonics...
The Issue: Stryker received two reports indicating that during screw insertion under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Respiratory Virus Plus Nucleic Acid Test (RV+) on Recalled by...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Recalled...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-UP) performed...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Mixing Cup Arrays utilized on VITROS 250 Recalled...
The Issue: Ortho Clinical Diagnostics issued a product correction notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.