Product Recalls in Colorado
Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,432 recalls have been distributed to Colorado in the last 12 months.
Showing 40981–41000 of 51,434 recalls
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: 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: 4" Microbore Double Lumen Set with Bionector 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: 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: 7" High Pressure Set with Bionector 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: 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: Bifurcated set with check vales and Bionectors 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: 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: 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: N Latex IgM Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Complaints have been confirmed on failed proficiency testing due to serum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TDX 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: 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: 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: 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: Culinary Masters Recalled by Gourmet Foods International Due to Undeclared...
The Issue: Products were manufactured with cumin found to contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Culinary Masters Recalled by Gourmet Foods International Due to Undeclared...
The Issue: Products were manufactured with cumin found to contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Culinary Masters Recalled by Gourmet Foods International Due to Undeclared...
The Issue: Products were manufactured with cumin found to contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Culinary Masters Recalled by Gourmet Foods International Due to Undeclared...
The Issue: Products were manufactured with cumin found to contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Culinary Masters Recalled by Gourmet Foods International Due to Undeclared...
The Issue: Products were manufactured with cumin found to contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Culinary Masters Recalled by Gourmet Foods International Due to Undeclared...
The Issue: Products were manufactured with cumin found to contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.