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. 2,369 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,369 in last 12 months

Showing 1982119840 of 47,027 recalls

Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products K+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· MEDTECH SAS

Recalled Item: Rosa Brain 3.0 Recalled by MEDTECH SAS Due to The instrument holder may be...

The Issue: The instrument holder may be sent on a trajectory that is not within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1400-04. For Recalled...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1700-10. For Recalled...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For Recalled...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1500-04-S. For...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1300-04-S. For...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a / 980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Exactech, Inc.

Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...

The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2019· West-Ward Columbus Inc

Recalled Item: Oxcarbazepine Oral Suspension Recalled by West-Ward Columbus Inc Due to...

The Issue: Failed Impurities/Degradation Specificattion

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Darmerica, LLC

Recalled Item: Quinacrine Dihydrochloride (98.25%) Recalled by Darmerica, LLC Due to Label...

The Issue: Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 6, 2019· Cardinal Health dba Specialty Pharmaceutical Services

Recalled Item: Nucala (mepolizumab) Injection Recalled by Cardinal Health dba Specialty...

The Issue: Temperature Abuse; Product stored and shipped outside of labeled storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Torrent Pharma Inc.

Recalled Item: Anagrelide Capsules Recalled by Torrent Pharma Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High Out Of Specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Mylan Pharmaceuticals Inc....

The Issue: Failed Impurities/Degradation Specifications:OOS for unknown impurity.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 6, 2019· Pfizer Inc.

Recalled Item: Bacteriostatic Water for Injection Recalled by Pfizer Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 6, 2019· ConAgra Foods, INc.

Recalled Item: Udi's Classic Hamburger Buns Recalled by ConAgra Foods, INc. Due to Foreign...

The Issue: potential presence of foreign material

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

Class II — Potential Health HazardOngoing
Refund