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. 2,742 recalls have been distributed to Michigan in the last 12 months.
Showing 1121–1140 of 29,286 recalls
Recalled Item: GORE ACUSEAL Vascular Graft Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Reports of vascular graft delamination, which may lead to reduced access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAC VU360 Acquisition Trunk Cable and Module Holder Recalled by GE Medical...
The Issue: If a user incorrectly places the Acquisition Module into the Acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyDay Toric Recalled by CooperVision, Inc. Due to One lot manufactured with...
The Issue: One lot manufactured with an invalid sterilization cycle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyant 1-Day Premium Toric Recalled by CooperVision, Inc. Due to One lot...
The Issue: One lot manufactured with an invalid sterilization cycle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofmed Breathables Recalled by CooperVision, Inc. Due to One lot...
The Issue: One lot manufactured with an invalid sterilization cycle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits: 1) VALVE PACK-LF Recalled by Medline Industries, LP Due to The...
The Issue: The kits contain certain lots of cannula products where the catheter may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venclose digiRF Generators Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Software version 3.35 of the Venclose digiRF Generator incorporates a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG6+ cartridge. List Number: 03P77-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG4+ cartridge (white). List Number: 03P85-25. Recalled by Abbott...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG7+ cartridge. List Number: 03P76-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MST ArcDUO 9mm Recalled by MicroSurgical Technology Inc Due to An ophthalmic...
The Issue: An ophthalmic knife has a suction set (not direct patient-contacting), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) with the below brands and product...
The Issue: Specific Automated Impella Controllers (AICs) that have a Pump Driver...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Recalled by...
The Issue: Some of the Vacuette¿ CAT Serum Separator Clot Activator tubes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.