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. 2,438 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,438 in last 12 months

Showing 1302113040 of 47,027 recalls

Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5 Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: SAFE-T PLUS ATRAUMATIC ADULT LP TRAY Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE DRUG FREE TRAY 22G Recalled by Bard Peripheral Vascular Inc...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY ADULT 18G X 3.5 Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G Recalled by Bard Peripheral...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL Recalled by Bard Peripheral...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray Recalled by Bard...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Envisiontec US Llc

Recalled Item: PCA 4000 Curing Units Recalled by Envisiontec US Llc Due to The PCA 4000 may...

The Issue: The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product...

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

Class II — Potential Health HazardOngoing
DrugJanuary 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed stability specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed stability specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Bortezomib Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed stability specifications

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

Class III — Low RiskOngoing
Refund
FoodJanuary 19, 2022· Amys Kitchen Inc

Recalled Item: Amy's Vegan Organic Rice Mac & Cheese Recalled by Amys Kitchen Inc Due to...

The Issue: Firm investigation detected trace amounts of milk through finished product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 19, 2022· Siemens Medical Solutions USA, Inc.

Recalled Item: Diagnostic Ultrasound System Recalled by Siemens Medical Solutions USA, Inc....

The Issue: The clip store function in the ultrasound imaging system does not work when...

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

Class II — Potential Health HazardOngoing
DrugJanuary 18, 2022· Teva Pharmaceuticals USA

Recalled Item: Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10...

The Issue: Failed Dissolution Specification: Dissolution results are below...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 18, 2022· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: LINQ II Insertable Cardiac Monitor Recalled by Medtronic Inc., Cardiac...

The Issue: Devices may lose functionality due to susceptibility to moisture ingress.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2022· Cytocell Ltd.

Recalled Item: Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions...

The Issue: individual components have been labelled with incorrect colours. The red and...

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

Class II — Potential Health HazardOngoing