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. 2,619 recalls have been distributed to Colorado in the last 12 months.
Showing 15201–15220 of 51,434 recalls
Recalled Item: OUTLOOK PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook¿ Pump 15 Drop 0.2 Micron Filtered IV Set with Recalled by B. Braun...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Pump Sets w/3 CARESITE Needle-Free Injection Sites: single-use for...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUMATCH CT CUT GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUMATCH CT PIN GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUMATCH CT FEM CUT TIB PIN R- TruMatch Patient Specific Recalled by DePuy...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUMATCH CT PIN GUIDE FEM R- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUMATCH CT CUT GUIDE FEM L- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUMATCH CT CUT GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Uncuffed Wire Endotracheal Tubes Recalled by Smiths Medical ASD Inc....
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access hsTnI High Sensitivity Troponin I Recalled by Beckman Coulter Inc....
The Issue: Through customer feedback, testing a sample with cardiac troponin I...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flourless Chocolate Torte Recalled by Gem City Fine Foods, LLC Due to...
The Issue: Frozen desserts are mislabeled. Flourless Chocolate Torte mislabeled with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Triple Berry Streusel Cheesecake Recalled by Gem City Fine Foods, LLC Due to...
The Issue: Frozen desserts are mislabeled. Flourless Chocolate Torte mislabeled with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...
The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...
The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.