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. 2,551 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,551 in last 12 months

Showing 2020120220 of 28,964 recalls

Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· C.R. Bard, Inc.

Recalled Item: SureStep Tray Recalled by C.R. Bard, Inc. Due to Labeling problem

The Issue: Labeling problem

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

Class III — Low RiskOngoing
Medical DeviceJune 28, 2016· CHG Hospital Beds Inc

Recalled Item: Spirit Plus Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical is...

The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Medtronic Xomed, Inc.

Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to Wire in...

The Issue: Wire in tubing can become exposed, posing potential harm to the intubated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· CHG Hospital Beds Inc

Recalled Item: Spirit Select Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical...

The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes 2.4mm Titanium Locking Screws Self-Tapping with Stardrive Recess...

The Issue: It was reported that the specified lots of the 2.4mm Titanium Locking Screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Trumpet Handpiece only Recalled by ConMed Corporation Due to The...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece Y-Tubing set Recalled by ConMed...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· Zimmer Gmbh

Recalled Item: TWIST DR 25X95MM Cann 12MM Thd 30MM AO Recalled by Zimmer Gmbh Due to Zimmer...

The Issue: Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· Zimmer Gmbh

Recalled Item: TWIST D 28X150MM CBS 45 Cann 14 MM AO Recalled by Zimmer Gmbh Due to Zimmer...

The Issue: Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· Cardinal Health

Recalled Item: The 9025TRU Arterial Blood Gas (ABG) Kit is used to Recalled by Cardinal...

The Issue: Arterial Blood Gas (ABG) Kit- Missing Safety Component. The ABG Kit(s) have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· Zimmer Gmbh

Recalled Item: V-TEK TWIST D 40X90MM 30MM Cann 12MM Rnd Recalled by Zimmer Gmbh Due to...

The Issue: Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· Zimmer Gmbh

Recalled Item: V-TEK TWIST D 3.5X90MM 30MM Can 12MM Rnd Recalled by Zimmer Gmbh Due to...

The Issue: Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist...

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

Class II — Potential Health HazardOngoing