Moses Lake Professional Pharmacy Recalls Injectable Vitamin and Lidocaine Solution
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 30 mL vials of an injectable solution containing vitamins, lidocaine, and other compounds due to a lack of assurance of sterility.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II and involves a lack of assurance of sterility in an injectable drug, which poses a significant risk of serious health consequences such as infection.
Plain-English summary
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 30 mL vials of an injectable solution containing B1, B2, B3, B5, B12, lidocaine, isoleucine, methionine, choline, and inositol. The product is a prescription-only compounded drug manufactured in Moses Lake, Washington.
The recall was initiated because there is a lack of assurance of sterility for the product. The source text indicates that all sterile human compounded drugs within their expiry date are affected by this issue.
Consumers who have this product should stop using it and contact their healthcare provider or the pharmacy for further instructions. The recall is classified as FDA Class II.
The recalled product
- Product
- B1/B2/B3/B5/B12/LIDOCAINE/ISOLEUCINE/METHIONINE/CHOLINE/INOSITOL, Injectable Solution, 50/5/50/5/1/10/25/8/17/17 MG/ML, 30 mL vial, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
- Category
- Drug — Compounded Injectable
- Affected units
- 5
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 (1)
- t05122015@3
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 101 recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy under a single FDA (Drugs) 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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