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. 2,537 recalls have been distributed to Michigan in the last 12 months.
Showing 20341–20360 of 29,286 recalls
Recalled Item: Large QWIX Compression screw Recalled by Integra LifeSciences Corp. Due to...
The Issue: Labeling on the Qwix Screw product states that it is a "compression screw"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enzymatic Cholesterol (Trinder/COD-CEH) for IN VITRO DIAGNOSTIC USE in the...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Power Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Brain 3.0.0 Usage: The device is intended for the Recalled by Zimmer...
The Issue: Communication errors between ROSANNA BRAIN software, MARIO software and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLUE IMPERVIOUS GOWN WITH THUMBHOOKS Recalled by Cardinal Health Due to Blue...
The Issue: Blue Impervious Gown with thumbhooks, X-large. All lots do not meet design...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urea Nitrogen/Color BUN (Enzymatic Berthelot) for IN VITRO DIAGNOSTIC USE...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Radiology CT Model number 728244 Product Usage: Computed...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
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: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for IN VITRO DIAGNOSTIC...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry XPT Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens identified an issue with the ratio equation provided on the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Recalled by...
The Issue: Incorrect drill protocol in the Instructions for Use (IFU)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.