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. 2,596 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,596 in last 12 months

Showing 1768117700 of 28,964 recalls

Medical DeviceJune 27, 2017· Cardinal Health 200, LLC

Recalled Item: Converters(R) Under Buttocks Drape with Fluid Control Pouch II Recalled by...

The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Cardinal Health 200, LLC

Recalled Item: Converters(R) Tiburon(R) Arthroscopy Drape Recalled by Cardinal Health 200,...

The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Certified Safety Mfg Inc

Recalled Item: Burn Sheet Recalled by Certified Safety Mfg Inc Due to Burn Sheet has...

The Issue: Burn Sheet has possibility of being shredded.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Beckman Coulter Inc.

Recalled Item: Coulter LH 750 Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 6 x 25 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Beckman Coulter Inc.

Recalled Item: Coulter HmX CP and Coulter HmX AL Analyzers The purpose Recalled by Beckman...

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Spectra-System/Legacy Guided Surgery Handle Kit Recalled by Implant Direct...

The Issue: The inside diameter of the 2.3mm small drill guide inserts have a smaller...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Ameditech Inc

Recalled Item: Alere iScreen Dx Urine Drug Screen Card Recalled by Ameditech Inc Due to The...

The Issue: The kit box label incorrectly identifies PCP (instead of TCA) as one of the...

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

Class III — Low RiskOngoing
Medical DeviceJune 26, 2017· Encore Medical, Lp

Recalled Item: Cobalt MV with Gentamicin Recalled by Encore Medical, Lp Due to Loss of the...

The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Encore Medical, Lp

Recalled Item: Cobalt HV Bone Cement 40GM Recalled by Encore Medical, Lp Due to Loss of the...

The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Encore Medical, Lp

Recalled Item: Cobalt MV Bone Cement 40GM Recalled by Encore Medical, Lp Due to Loss of the...

The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Encore Medical, Lp

Recalled Item: Cobalt HV with Gentamicin Recalled by Encore Medical, Lp Due to Loss of the...

The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· Exactech, Inc.

Recalled Item: Truliant Tibial Trial Handle. To assist the surgeon in the Recalled by...

The Issue: The Truliant Tibial Trial Handle's pin may disassociate from the main body.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing