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. 1,057 recalls have been distributed to Michigan in the last 12 months.
Showing 17301–17320 of 53,342 recalls
Recalled Item: SD-240U-25 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-200H-8022 22G EZSHOT ASPIRATION NEEDLE Recalled by Aomori Olympus Co.,...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-204 GUIDE SHEATH KIT 2.6MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B5-2Q BALLOON CATHETER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-202 GUIDE SHEATH Kit 2.0MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B7-2Q BALLOON CATHETER 13MM DIA 3.2 Recalled by Aomori Olympus Co., Ltd. Due...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 25G 6MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KD-650L ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life...
The Issue: A gluten free claim was inadvertently used on the lid of the container....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorhexidine Gluconate Oral Rinse USP 0.12% Recalled by Precision Dose Inc....
The Issue: cGMP deviations: The firm was notified of the manufacturer's expanded recall.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz Recalled by...
The Issue: Labeling: Missing instructions for use insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Injection 1 Recalled by AuroMedics Pharma LLC Due to...
The Issue: Discoloration and failed pH specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG - Product Recalled by Beckman...
The Issue: The Quality Control (QC) card has a label error for the standard deviation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tourni-Cot - Universal Recalled by Mar-Med Co Due to A failure can occur if...
The Issue: A failure can occur if the user attempts to remove the device by partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm...
The Issue: Potential for the battery to lose its ability to be recharged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paroex (Chlorhexidine Gluconate) Oral Rinse Recalled by Sunstar Americas,...
The Issue: cGMP Deviations; FDA inspection of manufacturing facility observed potential...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam Oral Solution Recalled by Akorn, Inc. Due to Defective...
The Issue: Defective container: Customer complaints for oral solution leaking from bottles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc...
The Issue: Control panel arm assembly could have missing or loose screws where undue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHILIPS Incisive Computed tomography X-ray system Incisive CT Software...
The Issue: Patient tabletop moved out to the home position during scan initialization,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.