Product Recalls in Michigan
Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,532 recalls have been distributed to Michigan in the last 12 months.
Showing 28201–28220 of 53,342 recalls
Recalled Item: Nicolet¿ Ambulatory EEG Recalled by Natus Neurology Inc Due to Potential to...
The Issue: Potential to be able to import an ambulatory exam for a patient for which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Spirit(Model 10045692 ) Recalled by Siemens Medical Solutions USA,...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective (Model 10495568) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daisho Kimchi Hot Pot Soup Base Recalled by J F C International Inc Due to...
The Issue: Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: StoneBreaker C02 Cartridge Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Probe Cap Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Pneumatic Lithotripter Recalled by Cook Inc. Due to The...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Exhaust Line Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Sterilization Cap Recalled by Cook Inc. Due to The interior of...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Single Use Probe Recalled by Cook Inc. Due to The interior of...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Exhaust Cap Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Calcium Flex¿ reagent cartridge Recalled by Siemens...
The Issue: May produce erroneously low results from specific well sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee...
The Issue: Customers may receive the incorrect size implant from what is labeled on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: Broken or missing screws and retaining clips. This may be due to screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VELCADE (bortezomib) for injection Recalled by Millennium Pharmaceuticals...
The Issue: Defective Container: Confirmed reports of loose vial crimps.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets 20 mg Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System. 75 mcg/h Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets 40 mg Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets 10 mg Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.