Pharmatech Recalls Pedia Poly-Vite Drops Due to Potential Bacterial Contamination
Pharmatech LLC is recalling 6,600 bottles of Pedia Poly-Vite Drops due to a potential risk of contamination with Burkholderia cepacia.
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 described as a precautionary measure due to potential contamination, which aligns with the rubric for voluntary precautionary recalls.
Plain-English summary
Pharmatech LLC is recalling 6,600 bottles of Pedia Poly-Vite Drops, 50 mL, OTC Non-Sterile, a dietary supplement. The recall was initiated as a precautionary measure due to a potential risk of product contamination with Burkholderia cepacia.
The affected product is identified by NDC No. 76518-030-50, Lot No. 20701512, and an expiration date of 11/2017. The product was distributed in Florida, Michigan, Mississippi, and Ohio.
Consumers who have this product should stop using it and contact Pharmatech LLC for further instructions.
The recalled product
- Product
- Pedia Poly-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
- Manufacturer
- Pharmatech LLC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 6,600
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 (3)
- NDC No. 76518-030-50
- Lot No. 20701512
- Exp. Date 11/2017.
Distribution
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.
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