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. 2,471 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,471 in last 12 months

Showing 1298113000 of 13,356 recalls

DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Best Choice Health Care Recalled by Raritan Pharmaceuticals, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Wal-Mucil Plus Calcium Fiber Capsules Recalled by Raritan Pharmaceuticals,...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Berkley & Jensen Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc....

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Equate Fiber Therapy Recalled by Raritan Pharmaceuticals, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Premier Value Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc. Due...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Leader Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter; product may contain fibrous material

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 29, 2012· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: A single visible particulate was observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2012· Bristol-myers Squibb Company

Recalled Item: BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only Recalled by...

The Issue: Superpotent (Single Ingredient) Drug: All BiCNU lots within expiration which...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 28, 2012· James G. Cole, Inc.

Recalled Item: I-C Drops Recalled by James G. Cole, Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: The product is being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2012· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2012· Hospira Inc.

Recalled Item: Preservative-Free MORPHINE Sulfate Injection Recalled by Hospira Inc. Due to...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2012· Samantha Lynn, Inc

Recalled Item: Reumofan Plus Tablets Recalled by Samantha Lynn, Inc Due to Undeclared Drug

The Issue: Marketed without an approved NDA/ANDA: Samantha Lynn Inc. is recalling...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights Recalled by Evol Nutrition Due to Marketed Without an Approved...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Ferring Pharmaceuticals Inc

Recalled Item: Novarel¿ (Chorionic Gonadotropin for injection Recalled by Ferring...

The Issue: Labeling; incorrect or missing insert; Warnings portion of the Package...

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

Class III — Low RiskOngoing
Refund
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights for Her Recalled by Evol Nutrition Due to Marketed Without an...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Adulterated...

The Issue: Adulterated Presence of Foreign Tablets: A product complaint was received by...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2012· Hospira Inc.

Recalled Item: HYDROmorphone HCl Injection Recalled by Hospira Inc. Due to Superpotent...

The Issue: Superpotent (Single Ingredient) Drug: The prefilled cartridge unit has been...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 15, 2012· Galderma Laboratories, L.P.

Recalled Item: Capex Shampoo (fluocinolone acetonide) Recalled by Galderma Laboratories,...

The Issue: Subpotent; fluocinolone acetonide.

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

Class III — Low RiskOngoing
Refund
DrugAugust 14, 2012· Bracco Diagnostic Inc

Recalled Item: Choletec - Kit for the Preparation of Technetium Tc 99m Mebrofenin Recalled...

The Issue: Presence of Particulate Matter; potential for charcoal particulates

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

Class III — Low RiskOngoing
Refund