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. 2,489 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,489 in last 12 months

Showing 3362133640 of 51,434 recalls

Medical DeviceAugust 9, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...

The Issue: Communication provided to emphasize that the PSA values should be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 Recalled by Mentor...

The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 Recalled by Mentor...

The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Diocto Syrup (docusate sodium) Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Sennazon (sennosides) Syrup Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Aller-Chlor (chlorpheniramine maleate) Syrup Recalled by Pharmatech LLC Due...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof (chlophedianol HCl and pyrilamine maleate) Liquid Recalled by...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Senexon Liquid (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof-A (acetaminophen Recalled by Pharmatech LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Senna Syrup (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2016· Becton Dickinson & Company

Recalled Item: BD 23 G x .75 in. BD Vacutainer¿ Push Button Recalled by Becton Dickinson &...

The Issue: BD has received multiple reports of units associated with the 23 G x .75 in....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Permits access...

The Issue: Shipping carton labeling error.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Calibrator U Recalled by Siemens Healthcare...

The Issue: Failure of analytical sensitivity with Calibrator U kit lots ending in 63...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Module Model 8110 with software version 9.15 The Recalled by...

The Issue: A software anomaly with the Alaris Syringe module software version 9.15 may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Arrow International Inc

Recalled Item: Arterial Line Catheterization Kit with Sharps Safety Features Permits access...

The Issue: Shipping carton labeling error.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 5, 2016· Teva North America

Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America Due to...

The Issue: Failed Impurities/Degradation Specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 5, 2016· Medtronic Inc.

Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...

The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Riverpoint Medical, LLC

Recalled Item: Nylon Surgical Suture for human use and vet use Recalled by Riverpoint...

The Issue: Nylon Surgical Sutures are recalled because the seals may become open during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing