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 2574125760 of 47,027 recalls

Medical DeviceDecember 12, 2017· Boston Scientific Corporation

Recalled Item: Malecot Nephrostomy Catheter Set Recalled by Boston Scientific Corporation...

The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Boston Scientific Corporation

Recalled Item: Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is Recalled...

The Issue: Potential polymer material degradation.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Whipknot Soft Tissue Cinch #5 Sutures. PN: 7211015 Recalled...

The Issue: Packaging design is insufficient to prevent potential sterile barrier breach...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Philips Electronics North America Corporation

Recalled Item: digital x-ray detector ProGrade R1 - solid state X ray Recalled by Philips...

The Issue: It the WiFi connection between the SkyPlate detector and HP transfer point...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2017· Sanofi Genzyme

Recalled Item: Synvisc-One ¿ (hylan G-F 20) Recalled by Sanofi Genzyme Due to Contamination...

The Issue: Contamination with Methylbacterium thiocyanatum

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Datex-Ohmeda, Inc.

Recalled Item: CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The...

The Issue: Potential for the display processor to experience an unexpected failure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Humeral Stem 83mm(Size 17) Product Usage: Intended for primary and Recalled...

The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Humeral Stem 55mm(Size 13) Product Usage: Intended for primary and Recalled...

The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c8000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c16000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Remel Inc

Recalled Item: Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum Recalled by Remel Inc...

The Issue: The serum may fail to agglutinate within the specified minimum reaction time.

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena deep clean purifying whipped foam cleanser Recalled by Johnson &...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena Acne Proofing whipped foam cleanser Recalled by Johnson & Johnson...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· BotanicalNow

Recalled Item: BodySlim Herbal Advanced technology & Strong formula capsules Recalled by...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 7, 2017· SCA Pharmaceuticals

Recalled Item: Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - product label was...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 7, 2017· Ventura Foods, LLC

Recalled Item: Sysco Imperial Glazed Hot Bacon Dressing Recalled by Ventura Foods, LLC Due...

The Issue: A plastic foreign object was inadvertently introduced into the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 7, 2017· Ventura Foods, LLC

Recalled Item: Sysco Imperial Tartar Sauce Recalled by Ventura Foods, LLC Due to Foreign...

The Issue: A plastic foreign object was inadvertently introduced into the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 7, 2017· Ventura Foods, LLC

Recalled Item: Classic Gourmet Dressing Recalled by Ventura Foods, LLC Due to Foreign...

The Issue: A plastic foreign object was inadvertently introduced into the product...

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

Class II — Potential Health HazardOngoing
Refund