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. 2,532 recalls have been distributed to Michigan in the last 12 months.
Showing 22821–22840 of 29,286 recalls
Recalled Item: GE Healthcare Innova IGS 630. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph. The ELI 380 is intended to be a high-performance...
The Issue: Mortara Instrument, Inc. has recently become aware of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 530. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System software RayStation is a...
The Issue: An error caused by a floating point precision problem tends to cause a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon PS X3 Tibial Insert Recalled by Stryker Howmedica Osteonics Corp....
The Issue: Stryker Orthopaedics received a report that 5537-G-319 No 3. Triathlon TS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima IGS 320. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite F500 Recalled by Tecan US, Inc. Due to A firmware bug causes...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite 200 PRO in vitro diagnostic. Product Usage: The Tecan Recalled by...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Cleaver Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 200¿M Lithotripsy Fiber- Reusable Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.