Moses Lake Pharmacy Recalls Dexpantenol Injectable Solution Due to Sterility Concerns
JD & SN Inc. is recalling 6 syringes of Dexpantenol Injectable Solution because the FDA identified 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 risk of serious injury or death from infection, meeting the criteria for a Severe rating.
Plain-English summary
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 6 syringes of Dexpantenol, Injectable Solution, 250 MG/ML, 30 mL. The product is prescription-only and was distributed nationwide. The recall was initiated due to a lack of assurance of sterility, which applies to all sterile human compounded drugs within their expiry date.
The FDA has classified this recall as Class II. Consumers and healthcare providers should stop using the affected product and contact the recalling firm or their healthcare provider for further instructions.
The recalled product
- Product
- DEXPANTHENOL, Injectable Solution, 250 MG/ML, 30 mL syringes, 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
- Affected units
- 6
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)
- t05282015@25
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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