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. 2,517 recalls have been distributed to Michigan in the last 12 months.
Showing 34401–34420 of 53,342 recalls
Recalled Item: SIEMENS IMMULITE/IMMULITE 1000 Systems Rubella IgM (RUM) Recalled by Siemens...
The Issue: Siemens received multiple customer complaints indicating an increase in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.2 Micron Filter Recalled by Baxter Corporation Englewood Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kits Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences has been notified of a medical device recall by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK¿ Horizon" Manual-Load Ligating Clip Applier Recalled by Teleflex...
The Issue: Misbranded: Incorrect etching on the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integral Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ventricular Catheter Accessory Kit Recalled by Integra LifeSciences...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Drainage Accessory Kits Recalled by Integra LifeSciences Corp. Due...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Straight Ventricular Catheter F8 Recalled by Integra LifeSciences...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSA Dissectron Fingertip Laparoscopic Cannula Recalled by Integra...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The EKOS cart has the catalog number 700-60101. The EKOS Recalled by EKOS...
The Issue: Casters on the EKOS carts may be missing washers which can cause premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera Biopsy Device Recalled by Hologic, Inc Due to Incorrect label on the...
The Issue: Incorrect label on the Sertera Biopsy Kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamotrigine Orally Disintegrating Tablets (ODT) Recalled by Impax...
The Issue: Labeling; Label Mixup; box labeled to contain 200 mg blister packs but...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.