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. 1,124 recalls have been distributed to Colorado in the last 12 months.
Showing 13461–13480 of 28,964 recalls
Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 410 Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 133 Tissue Expanders (also named style 133 BIOSPAN Tissue Recalled...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc. Due to...
The Issue: Potential for Hemospray device to be unable to spray powder due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 510 Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGhan BioDIMENSIONAL silicone-Filled Breast Implants Recalled by Allergan...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle Recalled by Allergan PLC Due to The action was initiated following...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Komuro Recalled by Allergan PLC Due to The action was initiated following...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 150 Full Height and Short Height Implants Recalled by Allergan PLC...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan 410 TruForm 2 (Soft Touch) BIOCELL breast implant...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle Inspira Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implants Recalled by Allergan PLC...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGhan Croissant-Shaped Tissue Expanders Recalled by Allergan PLC Due to The...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RITZ PRINCESS Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle133 Plus Tissue Expander With/Without Suture Tabs Recalled by...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Online TDM Vancomycin Gen.3 ( 200 tests) Catalog # 06779344190 Recalled by...
The Issue: Inaccurately Low Sample Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190...
The Issue: Inaccurately Low Sample Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.