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. 2,627 recalls have been distributed to Michigan in the last 12 months.
Showing 20101–20120 of 53,342 recalls
Recalled Item: BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Diacetate Injectable Suspension Recalled by Fusion IV...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylcobalamin Injection Recalled by Fusion IV Pharmaceuticals, Inc. dba...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotinamide Adenine Dinucleotide (PF) Injection Recalled by Fusion IV...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hungry Root Dairy free Garlic Parm sauce Recalled by The Honest Stand Due to...
The Issue: Undeclared Allergen: Product contains both cashews and almonds, but only...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth...
The Issue: The catheter locks for the lot may contain an 8Fr catheter lock instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 Recalled by...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 3mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 Recalled by...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Bluntfill with Filter Recalled by Cardinal Health 200, LLC Due to...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG4+ cartridge (blue) Recalled by Abbott Point Of Care Inc. Due to...
The Issue: The I-STAT BLUE CHEM8+ and CG4+ cartridges are not FDA cleared and do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CHEM8+ cartridges (blue) Recalled by Abbott Point Of Care Inc. Due to...
The Issue: The I-STAT BLUE CHEM8+ and CG4+ cartridges are not FDA cleared and do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural Catheterization Kit with FlexTip Plus Recalled by Arrow...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Set for Pediatric Lumbar Placement...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraCath Epidural Catheterization Kit Recalled by Arrow International Inc...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.