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. 2,492 recalls have been distributed to Michigan in the last 12 months.
Showing 39021–39040 of 53,342 recalls
Recalled Item: PenBlade Safety Scalpel Recalled by Zien Medical Technologies, Inc Due to...
The Issue: Cracks were discovered in the PET tray of a small population of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid...
The Issue: Some devices exhibit backup VVI operation due to a backup reset.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC PERFUSION TUBING PACKS (with potentially affected...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIVATORS HEMOCOR HPH700 Recalled by Medtronic Perfusion Systems Due to...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cevimeline Hydrochloride Capsules Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Stability Specifications: product may not meet specification limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution Recalled by Bausch & Lomb, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CIOS ALPHA Recalled by Siemens Medical Solutions USA, Inc Due to patient...
The Issue: patient procedure interruption due to a potential system failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System P4 software Recalled by Intuitive Surgical, Inc....
The Issue: Complaints regarding the Exposed Knife Blade recoverable fault for the Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturipe Foods Frozen Blueberries Recalled by MBG Marketing Due to Potential...
The Issue: MBG Marketing is recalling select pallets of Naturipe IQF Blueberries due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caravelle ABC Cookies Banh Chu NET WT: 7oz (200gr) Product of Vietnam...
The Issue: Anhing Corporation is recalling Caravelle ABC Cookies because recent...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems Recalled by...
The Issue: When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMR Shoulder/Spalla Trial Heads ECC .4 mm Adaptor Recalled by Limacorporate...
The Issue: The dimensions of the mating features of the recalled products are out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMR Shoulder/Spalla Trial Humeral Head diameter .42 mm Recalled by...
The Issue: The dimensions of the mating features of the recalled products are out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bactroban Ointment (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due...
The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...
The Issue: Subpotent Drug: Subpotent atorvastatin.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...
The Issue: Subpotent Drug: Subpotent atorvastatin.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bactroban Cream (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due to...
The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.