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. 2,418 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,418 in last 12 months

Showing 4618146200 of 51,434 recalls

Medical DeviceAugust 29, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...

The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Steris Corporation

Recalled Item: Reliance Endoscope Processing System (REPS) Recalled by Steris Corporation...

The Issue: The air pipe that delivers unfiltered ambient air from the procedure room...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens RAD Fluoro Uro System (Ysio Recalled by Siemens Medical Solutions...

The Issue: When using systems operating with software versions VD10A/G during a RAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· SpineFrontier, Inc.

Recalled Item: S-LIFT Extension Shims Extension shims are manufactured from grade 5...

The Issue: Fit variation among all lots of S-LIFT extension shims with corresponding...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Zimmer, Inc.

Recalled Item: VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys...

The Issue: Based on a review of historic packaging validations, it was determined that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Globus Medical, Inc.

Recalled Item: Globus Medical MicroFuse Putty Recalled by Globus Medical, Inc. Due to The...

The Issue: The sterility of this product to a Sterility Assurance Level (SAL) of 10(-6)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2013· Camlog Usa

Recalled Item: C2244.4308 CONELOG Titanium Base CC ¿4.3GH2 0.8 inkl HS Product Recalled by...

The Issue: Product not cleared for sale/use in the United States.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Camlog Usa

Recalled Item: C2244.5008 CONELOG Titanbasis CAD/CAM Conelog Titanium Base CAD/CAM Rx only...

The Issue: Product not cleared for sale/use in the United States.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Camlog Usa

Recalled Item: C2244.3820 Recalled by Camlog Usa Due to Product not cleared for sale/use in...

The Issue: Product not cleared for sale/use in the United States.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Camlog Usa

Recalled Item: C2244.3808 Recalled by Camlog Usa Due to Product not cleared for sale/use in...

The Issue: Product not cleared for sale/use in the United States.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Carefusion 2200 Inc

Recalled Item: *** 1) Cat. 4341B Recalled by Carefusion 2200 Inc Due to Catheters included...

The Issue: Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray -...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· Siemens Healthcare Diagnostics

Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· Siemens Healthcare Diagnostics

Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Captia Syphilis-G Test Kit Product Usage: This is an enzyme Recalled by...

The Issue: Trinity Biotech recalled Trinity Biotech Captia Syphilis IgG kits due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· H & H Associates

Recalled Item: H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01 Recalled by H &...

The Issue: Medical device tubing used for endotracheal airway application may become...

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

Class I — Serious Health HazardOngoing
DrugAugust 26, 2013· Leiter's Pharmacy

Recalled Item: Lidocaine/Phenylephrine PF 1%/1.5% Injectible vials Recalled by Leiter's...

The Issue: Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2013· Leiter's Pharmacy

Recalled Item: Dextrose 50% Preservative Free SDV Injection Solution Recalled by Leiter's...

The Issue: Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2013· Leiter's Pharmacy

Recalled Item: Hyaluron (hyaluronidase) 150 units/mL Preserved Solution Recalled by...

The Issue: Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2013· Leiter's Pharmacy

Recalled Item: Bevacizumab (Avastin) 2.5mg/0.1mL PF Inj. Recalled by Leiter's Pharmacy Due...

The Issue: Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial...

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

Class II — Potential Health HazardOngoing
Refund