The Recall Desk
ModerateFDA (Food)·F-0263-2017·Announced 2016-11-02

Pharmatech Recalls Tri-Vitamin Dietary Supplement Due to Potential Contamination

Pharmatech LLC is recalling Tri-Vitamin dietary supplement bottles due to a precautionary measure regarding potential Burkholderia cepacia contamination.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II and is explicitly described as a precautionary measure with no reported illnesses or injuries, fitting the criteria for a moderate severity score.

Plain-English summary

Pharmatech LLC is recalling 105,456 bottles of Tri-Vitamin, 50 mL, OTC Non-Sterile dietary supplement. The recall was initiated as a precautionary measure due to the potential risk of product contamination with Burkholderia cepacia.

The affected product is identified by UPC No. 005368501800. The recall includes three specific lots: Lot No. 20731506 with an expiration date of 08/2017, Lot No. 20731603 with an expiration date of 02/2018, and Lot No. 20731604 with an expiration date of 06/2018.

The product was distributed in Florida, Michigan, Mississippi, and Ohio. Consumers should check their inventory for the specific lot numbers and expiration dates listed above and stop using the product if it matches the recalled items.

The recalled product

Product
Tri-Vitamin, 50 mL, OTC Non-Sterile. Dietary supplement.
Manufacturer
Pharmatech LLC
Affected units
105,456

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (7)

  • UPC No. 005368501800
  • Lot No. 20731506
  • Exp. Date 08/2017
  • Lot No. 20731603
  • Exp. Date 02/2018
  • Lot No. 20731604
  • Exp. Date 06/2018.

Distribution

Distributed in 4 states:

Part of a larger recall action

This product is one of 23 recalled by Pharmatech LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 23 products in this recall →