Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 967 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
967 in last 12 months

Showing 31921–31940 of 48,215 recalls

Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: SafeSet Kit with 30 mL Flush Device Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: 5 Port OFF Manifold with Transpac IV Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Monitoring Kit with TP4 Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet 84" Arterial Pressure Tubing...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Bifurcated Kit with SafeSet Reservoir Recalled by ICU Medical,...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 03 ml Squeeze Flush Recalled by ICU Medical,...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with SafeSet 84" Arterial Pressure Tubing...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Trifurcated Monitoring Kit with 84" SafeSet Reservoir Recalled...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Bifurcated SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Triple Line SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir and 2 Recalled...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet Reservoir and 2 Blood Sampling...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Single Monitoring Kit with 30mL Flush Device Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: TP4 Kit with 10cc SafeSet Reservoir Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· Blackrock Microsystems, LLC

Recalled Item: Neural Signal Amplifier. Part Numbers: 4208 Recalled by Blackrock...

The Issue: Blackrock Microsystems, LLC announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· Blackrock Microsystems, LLC

Recalled Item: Patient Cable. Part Numbers: 4460 Recalled by Blackrock Microsystems, LLC...

The Issue: Blackrock Microsystems, LLC announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
DrugAugust 10, 2016· Allergy Laboratories, Inc.

Recalled Item: Ephedrine Sulfate Injection Recalled by Allergy Laboratories, Inc. Due to...

The Issue: Lack of Assurance of Sterility: An FDA inspection at the facility raised...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue Recalled by...

The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Zimmer Biomet, Inc.

Recalled Item: Phoenix Recon Targeting Arm Guide Recalled by Zimmer Biomet, Inc. Due to Old...

The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...

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

Class II — Potential Health HazardOngoing