Pharmatech Recalls Pedia D-Vite Drops Due to Potential Contamination
Pharmatech LLC is recalling Pedia D-Vite Drops as a precaution due to potential 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 5,040 bottles of Pedia D-Vite Drops, 50 mL, OTC Non-Sterile. This product is a 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 NDC No. 76518-050-50, Lot No. 20691509, 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 D-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
- Manufacturer
- Pharmatech LLC
- Category
- Drug — Dietary Supplement
- Hazard
- Affected units
- 5,040
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. 76518-050-50
- Lot No. 20691509
- 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.
See all 23 products in this recall →Related recalls
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