Moses Lake Pharmacy Recalls Vitamin D3 Injectable Solution for Sterility Concerns
JD & SN Inc. is recalling 8 syringes of Vitamin D3 Oil Injectable Solution 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 infection or serious injury.
Plain-English summary
JD & SN Inc., doing business as Moses Lake Professional Pharmacy, is recalling 8 syringes of Vitamin D3 Oil, Injectable Solution, 50,000 UNITS/ML. The affected products include 6 syringes of 30 mL and 2 syringes of 10 mL. The recall was initiated because of a lack of assurance of sterility for all sterile human compounded drugs within their expiry dates.
The affected products were distributed nationwide. The specific lot codes involved are t10242014@16, t05282015@21, and t03182015@35. The FDA has classified this recall as Class II, indicating that use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences.
Consumers and healthcare providers should stop using the affected syringes and contact the recalling firm for further instructions or a refund.
The recalled product
- Product
- VITAMIN D3 OIL, Injectable Solution, 50,000 UNITS/ML, syringe sizes: 10 mL and 30 mL, Rx only,JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
- Category
- Drug — Injectable Solution
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)
- t10242014@16
- t05282015@21
- t03182015@35.
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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