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. 1,801 recalls have been distributed to Colorado in the last 12 months.
Showing 39181–39200 of 51,434 recalls
Recalled Item: Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triglycerides/Glycerol Blanked. In vitro test for the quantitative...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uric Acid plus ver.2 In vitro test for the quantitative Recalled by Roche...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LDL-Cholesterol gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol Gen.2. The cassette COBAS Integra Cholesterol Gen.2 (CHOL2)...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDL-Cholesterol plus gen.3. Recalled by Roche Diagnostics Operations, Inc....
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine Plus ver. 2. Intended for use on COBAS INTEGRA systems Recalled...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QVAR (beclomethasone dipropionate HFA 40 mcg) Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: syngo Workflow SLR Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential exists for order transactions from interfaced HIS (Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapidlab 1265 system is a blood gas analyzer used Recalled by Siemens...
The Issue: D50 and D51 diagnostic error codes are not functional.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapidlab 1260 system is a blood gas analyzer used Recalled by Siemens...
The Issue: D50 and D51 Diagnostic error codes are not functional.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.