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. 2,480 recalls have been distributed to Michigan in the last 12 months.
Showing 41721–41740 of 53,342 recalls
Recalled Item: 6" Trifurcated Extension Set Recalled by Churchill Medical Systems, Inc. Due...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Si Surgical System Recalled by Intuitive Surgical, Inc. Due to The...
The Issue: The Wall chart has been updated because it was noted that Wall Chart (PN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Trifurcated set with Bionectors and check valves Recalled by Churchill...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Standard Bore High Pressure Ext Set Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Storm Series Electric Wheelchair. Invacare FDX Recalled by Invacare...
The Issue: If the slack in the wires is not routed and secured correctly, flexing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" Trifurcated set with Bionectors Recalled by Churchill Medical Systems,...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore T-Port Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FDX Electric Wheelchair. Invacare FDX Recalled by Invacare Corporation Due...
The Issue: If the slack in the wires is not routed and secured correctly, flexing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bifircated Extension Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8" Standard Bore Ext Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely-depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI¿ Humidifier Adaptor Recalled by Teleflex Medical Due to Foreign...
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUA 540 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.