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. 2,647 recalls have been distributed to Michigan in the last 12 months.
Showing 16441–16460 of 53,342 recalls
Recalled Item: For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Recalled by INNOVA...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT CHEST TUBE TRAY. Medical convenience kit Recalled by Avid Medical,...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit Recalled by Avid...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 7T Recalled by INNOVA MEDICAL GROUP,...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: LVAD Dres Chg. MAI Kit Part Number: 79544B Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420 Recalled by...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Blood Culture. MAI Kit Part Number: 80315D Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Midline Insertion DA. MAI Kit Part Number: 77981B Recalled by Medical...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Injection REVIEW MAI Kit Part Number: 74736 Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Blood Culture MAI Kit Part Number: 80076 Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ginseng Power 5000 capsule Recalled by NSNY Distributor Inc Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Premium OrgaZEN 7000 capsule Recalled by NSNY Distributor Inc Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natrol Melatonin 3 mg Recalled by Natrol, LLC Due to One lot of ALA 300 mg...
The Issue: One lot of ALA 300 mg Cap-50 were labeled at Melatonin 3 mg Tab-60.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: J-Basket Premium Korean Seaweed Snack - Wasabi flavor on outer Recalled by J...
The Issue: Wasabi Flavor Seaweed snack is incorrectly packaged in Original Seaweed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene SARS-CoV-2 Catalog Number: 410700 IVD for real-time Reverse...
The Issue: Emergency Use Application (EUA) application withdrawn as false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene RNA Software Upgrade Kit Revogene RNA Software Upgrade USBs...
The Issue: Emergency Use Application (EUA) application withdrawn as false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Recalled by Smith...
The Issue: Mislabeled box contained a 6mm x 20mm screw instead of 6mm x 30mm screw
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.