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. 2,572 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,572 in last 12 months

Showing 99419960 of 27,833 recalls

Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SYSTEM. Item Number: 5479084...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: DEXCOM G6 SENSOR 3 PACK Item Number: 5447552 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: VAPORIZER VICKS 1.5GAL Item Number: 2354942 Recalled by Cardinal Health Inc....

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: BD UF PEN 32GX4MM 100 NANO Item Number: 4292272 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRA TEST STRIPS 25 COUNT Item Number: 3510443 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033 Recalled by Cardinal...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: FREESTYLE LANCETS 28G 100CT Item Number:2975670 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port Recalled by...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 60mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Due to...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.3 mL Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/60" (152 cm) Appx 2.2 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/Spiros¿ Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 5 IN (13cm) APPX 0.57 ml Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.2 ml Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 6.1 ml Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Spiros" Closed Male Luer - Product Usage: provides Recalled by ICU Medical,...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing