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. 2,332 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,332 in last 12 months

Showing 2450124520 of 47,027 recalls

Medical DeviceJune 4, 2018· Fx Solutions

Recalled Item: Fx SOLUTIONS CENTERED HEAD CoCr 50x19 Recalled by Fx Solutions Due to Breach...

The Issue: Breach in the external blister of certain lots of Humelock Offset Head 50 X...

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

Class II — Potential Health HazardOngoing
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· Apotex Inc.

Recalled Item: Fluticasone propionate Nasal Spray Recalled by Apotex Inc. Due to Presence...

The Issue: Presence of foreign substance: glass particles

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 5% Dextrose Injection Recalled by ICU Medical Inc Due to Lack of assurance...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.45% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 30, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Presence of Foreign Substance: A product complaint was received for a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 30, 2018· Baxter Healthcare Corporation

Recalled Item: FLOSEAL Special Applicator Tips in cartons labeled in part Recalled by...

The Issue: Baxter r recalled this device due to the use of an incorrect plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2018· Canon Medical System, USA, INC.

Recalled Item: Nuclear Magnetic Resonance Imaging Systems that are indicated for use...

The Issue: When using respiratory gating with Steady Mode ON in Spin Echo sequence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2018· Zeiss, Carl Inc

Recalled Item: Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope...

The Issue: Under certain circumstances, the firmware makes it possible for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile Recalled...

The Issue: Cap may be mislabeled with incorrect part number, although the correct part...

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

Class II — Potential Health HazardOngoing
DrugMay 29, 2018· Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...

The Issue: Resuspension problems: Out of specification for appearance and resuspendability.

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

Class III — Low RiskOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave Post-Shave Moisturizer (salicylic acid) Recalled by Shadow...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave (salicylic acid) Shave Cream Acne Shield Recalled by Shadow...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: X-Jow (menthol USP) Pain Gel Recalled by Shadow Holdings DBA Bocchi Labs Due...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave 3 Step Shaving System Recalled by Shadow Holdings DBA Bocchi Labs...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2018· Dean Foods, Inc.

Recalled Item: Baskin Robbins Mint Chocolate Chip Recalled by Dean Foods, Inc. Due to...

The Issue: Product may contain unlabeled coconut.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Tiro Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing