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. 2,471 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,471 in last 12 months

Showing 3750137520 of 51,434 recalls

Medical DeviceSeptember 15, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Medical Device Identification Card for SureScan pacemaker...

The Issue: Some Medical Device Identification Cards provided to SureScan pacemaker...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Biochemical Diagnostics Inc

Recalled Item: CONSULT(TM) diagnostics hCG CONTROLS Kit Recalled by Biochemical Diagnostics...

The Issue: CONSULT diagnostics hCG Controls have discrepant storage temperatures listed...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2015· Medtronic Navigation, Inc.

Recalled Item: P/N: 9735023 Recalled by Medtronic Navigation, Inc. Due to Specific use...

The Issue: Specific use conditions can increase the possibility of a screwdriver tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Smiths Medical ASD, Inc.

Recalled Item: PORT-A-CATH Plastic Hub Needles Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: The label on the lid stock of the individual needle packages for a portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore (Oncology & Radiology) Computed Tomography X-ray...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Encore Medical, Lp

Recalled Item: Turon Shoulder Impaction Fixture The Turon and RSP Recalled by Encore...

The Issue: During the Turon assembly, the impaction forces caused the polymer, black...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Medtronic Navigation, Inc.

Recalled Item: P/N: 9734856 Recalled by Medtronic Navigation, Inc. Due to Specific use...

The Issue: Specific use conditions can increase the possibility of a screwdriver tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16-Slice (Air) Computed Tomography X-ray systems. Intended to...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· CooperSurgical, Inc.

Recalled Item: MILEX PESSARY KIT Recalled by CooperSurgical, Inc. Due to The products have...

The Issue: The products have been identified to have incorrect size prints on the MILEX...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2015· Encore Medical, Lp

Recalled Item: Reverse Shoulder Prosthesis Stem Impaction Fixture The Turon Recalled by...

The Issue: During the assembly, the impaction forces caused the polymer, black acetal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Valeant Pharmaceuticals North America LLC

Recalled Item: Valeant Pharmaceuticals North America Model No. Spag-2 Small Particle Size...

The Issue: SPAG-2 6000 Lot J3522070 was released to commerce without being tested for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Flex Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2015· US Compounding Inc

Recalled Item: Prednisolone Sodium Phosphate PF Solution (1%) in 15 mL dropper bottle...

The Issue: Lack of Assurance of Sterility; The firm is recalling all sterile...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2015· US Compounding Inc

Recalled Item: Betamethasone SP PF (12 mg/mL) Recalled by US Compounding Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility; The firm is recalling all sterile...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2015· US Compounding Inc

Recalled Item: Omnipaque 300 (600 mg/2 mL) Recalled by US Compounding Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility; The firm is recalling all sterile...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2015· US Compounding Inc

Recalled Item: Tropicamide 1%/Phenylephrine 2.5% (tropicamide USP 10 mg/ phenylephrine HCL...

The Issue: Lack of Assurance of Sterility; The firm is recalling all sterile...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2015· US Compounding Inc

Recalled Item: Phenylephrine (1 mg/mL) Recalled by US Compounding Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility; The firm is recalling all sterile...

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

Class II — Potential Health HazardOngoing
Refund