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. 2,527 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,527 in last 12 months

Showing 2330123320 of 28,964 recalls

Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 10x40 Airway Stent System Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 3.5mm Threaded Cerclage Pin Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Endo Catch 10mm Recalled by EXP Pharmaceutical...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange Insufflation Needle Recalled by EXP Pharmaceutical...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Mayfield Disposable Skull Pin Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange Round Diamond Bur Extra Coarse Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange SECURESTRAP 5mm Absorbable Strap Fixation Device...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange ETS FLEX 45 ENDOSCOPIC ARTICULATING LINEAR CUTTER...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange -Suction Coagulator Recalled by EXP Pharmaceutical...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 2.15MMX22MM Fluted Spiral Router for CRANI-A...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Sybron Dental Specialties

Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...

The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange PT WIRE 300 Recalled by EXP Pharmaceutical Services...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2015· Tosoh Bioscience, Inc.

Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...

The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 9, 2015· CooperSurgical, Inc.

Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...

The Issue: Incorrect size printed on the Milex Pessary Kit packaging label

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare DigitalDiagnost System X-Ray Recalled by Philips Medical...

The Issue: The system is designed to emit a beep upon termination of an exposure....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...

The Issue: The system is designed to emit a beep upon termination of an exposure....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 Recalled...

The Issue: Possibility of image artifacts during data acquisition when using Adaptive...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo HX2 Temperature Management System provides temperature control of two...

The Issue: Malfunctioning mixing valve and loss of cooling and/or heating capability....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 8i Surgical Skin Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Brilliance iCT SP. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing