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. 2,522 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,522 in last 12 months

Showing 2368123700 of 51,434 recalls

DrugFebruary 15, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Etomidate Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Subpotent Drug.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 14, 2019· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Dimercaptopropanesulfonate Sodium (DMPS) Recalled by McGuff Compounding...

The Issue: Presence of Particulate Matter: Particulates observed in vials release for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS with Option syngo DE Scan for Single Recalled by...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Bard Peripheral Vascular Inc

Recalled Item: PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane...

The Issue: Complaints received that products packaged with the incorrect introducer...

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

Class II — Potential Health HazardOngoing
DrugFebruary 13, 2019· Perrigo New York, Inc.

Recalled Item: Ciclopirox shampoo 1% Recalled by Perrigo New York, Inc. Due to Failed...

The Issue: Failed Degradation/Impurities Specifications: Out of specification related...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 13, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lovastatin Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 13, 2019· Schwan's Global Supply Chain, Inc., Specialy Foods Plant

Recalled Item: Big Daddy s Bold Cheese Pizza Recalled by Schwan's Global Supply Chain,...

The Issue: Cheese pizza may contain plastic pieces.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 13, 2019· Bioventus, LLC

Recalled Item: BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device...

The Issue: The firm became aware of the potential for the products' sterile pouch to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· O-Two Medical Technologies, Inc.

Recalled Item: e700 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...

The Issue: There is a potential for the unit to catch fire due to one of the screen...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2019· O-Two Medical Technologies, Inc.

Recalled Item: e500 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...

The Issue: There is a potential for the unit to catch fire due to one of the screen...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2019· O-Two Medical Technologies, Inc.

Recalled Item: e600 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...

The Issue: There is a potential for the unit to catch fire due to one of the screen...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 610 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml Product Usage: The systems are intended for head Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml DR Product Usage: The systems are intended for Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 710 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing