Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,023 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,023 in last 12 months

Showing 15361–15380 of 47,027 recalls

DrugMarch 17, 2021· Alembic Pharmaceuticals Limited

Recalled Item: Telmisartan Tablets Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Labeling: Label-mixup

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 17, 2021· Real Water, Inc.

Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...

The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 17, 2021· Real Water, Inc.

Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...

The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
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
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Appx 0.50 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: 45" (114 cm) Appx 1.7 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· Cardinal Health Inc.

Recalled Item: OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326 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: 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· Cardinal Health Inc.

Recalled Item: ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862 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: FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877 Recalled...

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 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· 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
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Bag Spike Adapter w/Spiros" w/Red Cap 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
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Admin Set w/ClaveTM 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 4.1 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: Appx 1.0 ml Recalled by ICU Medical, Inc. Due to Due to molding defect,...

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