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. 2,322 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,322 in last 12 months

Showing 3164131660 of 47,027 recalls

Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Right Foot/30mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Proximal Foot/Left Recalled by Synthes (USA)...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Left Foot/30mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2016· Integra LifeSciences Corp.

Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...

The Issue: The affected K-wires do not meet specification requirements. Specifically,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2016· Merz North America, Inc.

Recalled Item: Radiesse (+) Lidocaine Recalled by Merz North America, Inc. Due to...

The Issue: Complaints reported of Radiesse (+) unable to be expelled from the syringe...

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

Class II — Potential Health HazardOngoing
FoodMay 20, 2016· Ultimate Nutrition, Inc.

Recalled Item: ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2016· Ultimate Nutrition, Inc.

Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2016· Ultimate Nutrition, Inc.

Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 19, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Ultimax DREX-ULT80 X-ray generator Recalled by Toshiba American...

The Issue: It was discovered that the generator of the system could possibly terminate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...

The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...

The Issue: It was discovered that the generator of the system could possibly terminate...

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

Class II — Potential Health HazardOngoing
DrugMay 19, 2016· West-Ward Columbus Inc

Recalled Item: Oxycodone HCl Recalled by West-Ward Columbus Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specification; 9 month stability

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

Class III — Low RiskOngoing
Refund
DrugMay 19, 2016· Galderma Laboratories, L.P.

Recalled Item: Doxycycline Recalled by Galderma Laboratories, L.P. Due to Labeling:...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot...

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

Class III — Low RiskOngoing
Refund
DrugMay 18, 2016· Teva North America

Recalled Item: Divalproex Sodium Delayed-release Tablets USP Recalled by Teva North America...

The Issue: Failed Tablet/Capsule Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 18, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Elekta, Inc.

Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...

The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: TCA Board Recalled by Carefusion 211 Inc dba Carefusion Due to CareFusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: Gas Delivery Engine (GDE) Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: Gas Delivery Engine (GDE)- Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard with Compressor ventilator- Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing