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. 2,551 recalls have been distributed to Colorado in the last 12 months.
Showing 19481–19500 of 28,964 recalls
Recalled Item: Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS system Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Hardware issue that may expose the User to a potential risk for serious...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS Lyse Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the AQUIOS Lyse Reagent Kit because it may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes....
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 Assay (50 test kit)-for use Recalled by Siemens...
The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...
The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Sterile Disposable Probes sold individually Recalled by Ultroid...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...
The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash system Recalled by Siemens Medical Solutions USA,...
The Issue: Hardware issue that may expose the user to a potential risk for serious...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConforMIS iTotal Cruciate Retaining (CR) Knee Replacement System Recalled by...
The Issue: Mislabeled: incorrect serial number on the F4 A/P cut guide iJig.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheridan/CF Recalled by Teleflex Medical Due to Labeling inconsistency -...
The Issue: Labeling inconsistency - units labeled with a 7mm tube may contain a size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...
The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...
The Issue: Sterility of the outer surface of the container compromised due to packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.