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 21241–21260 of 29,286 recalls
Recalled Item: Medica ISE Module Calibrant A Recalled by AMS Diagnostics, LLC Due to Lot...
The Issue: Lot was not functioning properly and not exhibiting the correct physical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOSCOPE BRUSH- KARL STORZ Flexible Cleaning Brush single-use Recalled by...
The Issue: Endoscope cleaning brush 11276CL may not fit resulting in an inability to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gomco Style Circumcision Clamp Trays is an instrument used to Recalled by...
The Issue: Two lots of Gomco Style Circumcision Clamp Trays, SSI-0034 and 10-1100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Vesa 75/100 adaptation with rotation is an accessory to Recalled by...
The Issue: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...
The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbia gamma camera system Product Usage: The Symbia gamma Recalled by...
The Issue: We received a customer complaint that Siemens reported via the MedWatch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...
The Issue: Dialyzer header leak due to possible improper torque
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...
The Issue: The firm has received one report of values for patient height and weight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...
The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...
The Issue: We received a customer complaint that Siemens reported via the MedWatch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.6 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 110" (279 cm) Appx 13.8 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TeleSentry Battery Recalled by Scottcare Corporation Due to The firm...
The Issue: The firm received a complaint of the battery exploding while recharging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx. 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 31" (79 cm) Appx. 3.4 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 74" (188cm) approximately 9.0ml Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rebound Cartilage Product Usage: Rebound Cartilage is an external knee...
The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.