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. 2,509 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,509 in last 12 months

Showing 2666126680 of 28,964 recalls

Medical DeviceMay 20, 2013· Steris Corporation

Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...

The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2013· Olympus America Inc.

Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...

The Issue: There is a possibility that the pump head was not shipped in the locked...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2013· RF Technologies, Inc.

Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....

The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2013· SpineFrontier, Inc.

Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...

The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS System (HCP) The CoaguChek XS System is intended Recalled by...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Plus System The CoaguChek XS Plus system for Recalled by Roche...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS System (PST) The CoaguChek XS PT test strips Recalled by Roche...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Pro System The CoaguChek XS Pro System (CoaguChek Recalled by...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· The Standing Company

Recalled Item: Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device...

The Issue: Power Superstand Standing Wheel chair, flex shaft (the flexible wand which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Cincinnati Sub-Zero Products Inc

Recalled Item: Blanketrol III Data Export Software Version 1.10 The Blanketrol III Recalled...

The Issue: During a customer inquiry regarding a beta version of the Bill Data Export...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Tosoh Smd Inc

Recalled Item: AIA Analyzer Pipette Tips used on Tosoh AIA-2000 Recalled by Tosoh Smd Inc...

The Issue: Visual inspection of the pipette tips indicated that some of the tips were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Two Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp. Due...

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Four Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp....

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing