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. 1,077 recalls have been distributed to Indiana in the last 12 months.
Showing 16341–16360 of 53,528 recalls
Recalled Item: Goose Creek Hand Sanitizer aloe Watermelon Lemonade Recalled by...
The Issue: Chemical contamination: product found to be contaminated with methanol (wood...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Goose Creek Hand Sanitizer aloe Melon Picnic Recalled by Scentsational Soaps...
The Issue: Chemical contamination: product found to be contaminated with methanol (wood...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Goose Creek Hand Sanitizer aloe Grape Soda Recalled by Scentsational Soaps &...
The Issue: Chemical contamination: product found to be contaminated with methanol (wood...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coconut Stand CoCo TKO Hand Sanitizer Recalled by Scentsational Soaps &...
The Issue: Chemical contamination: product found to be contaminated with methanol (wood...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Goose Creek Hand Sanitizer aloe Marshmallows Recalled by Scentsational Soaps...
The Issue: Chemical contamination: product found to be contaminated with methanol (wood...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olympus Sterile Optical Laser Fiber Recalled by Quanta System, S.p.A. Due to...
The Issue: Product sterility is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quanta System Sterile Optical Laser Fiber Recalled by Quanta System, S.p.A....
The Issue: Product sterility is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quanta System Sterile Optical Laser Fiber Recalled by Quanta System, S.p.A....
The Issue: Product sterility is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent Recalled by...
The Issue: In rare situations patients infected with high viral load of SARS CoV 2 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Better-Bladder (BB) Recalled by Circulatory Technology Inc. Due to The...
The Issue: The device is used as part of extracorporeal membrane oxygenation (ECMO)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.