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. 1,039 recalls have been distributed to Colorado in the last 12 months.
Showing 27841–27860 of 51,434 recalls
Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echosight Jansen-Anderson Intratubal Transfer Set Recalled by Cook Inc. Due...
The Issue: Certain lots of in vitro fertilization (IVF) products were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmunoCAP Allergen c6 Recalled by Phadia US Inc Due to The stability...
The Issue: The stability specifications of ImmunoCAP Allergen c6, Amoxicilloyl were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular E 170 Analyzer: Immunoassay Chemistry Analyzer Recalled by Roche...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: c6000 Recalled by Roche Diagnostics Corporation Due to Complaints have been...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmunoCAP Allergen c5 Recalled by Phadia US Inc Due to The stability...
The Issue: The stability specifications of ImmunoCAP Allergen c5, Ampicilloyl were not met.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....
The Issue: Package integrity failure observed during routine shift package integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...
The Issue: if the cables of the Monica IF24 System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor - Monica Novii Wireless Patch System...
The Issue: if the cables of the Monica Novii System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Model 882482 Product Usage: BrightView XCT is a Recalled by...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW ENDURANCE" Extended Dwell Peripheral Catheter System Recalled by Arrow...
The Issue: Certain lots of peripheral catheter systems may be missing the safety latch,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.