Moses Lake Pharmacy Recalls Hydroxocobalamin Syringes Due to Sterility Concerns
JD & SN Inc. is recalling Hydroxocobalamin syringes because the FDA cannot assure the products are sterile.
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 injectable drugs, which poses a significant risk of serious health consequences such as infection.
Plain-English summary
JD & SN Inc., doing business as Moses Lake Professional Pharmacy, is recalling Hydroxocobalamin (preservative free) unit dose syringes. The recall is due to a lack of assurance of sterility for all sterile human compounded drugs within their expiration dates.
The affected product is an injectable solution with a concentration of 3 mg/0.25 mL. The recall includes syringe sizes of 20 mL and 30 mL. The specific quantity involved is three 30 mL syringes and one 20 mL syringe. The products are prescription-only and were distributed nationwide.
Consumers and healthcare providers should stop using these syringes and contact the recalling firm for further instructions. The FDA has classified this as a Class II recall.
The recalled product
- Product
- HYDROXOCOBALAMIN (PRESERVATIVE FREE) UNIT DOSE SYRINGES, Injectable Solution, 3 mg/0.25 mL, syringe sizes: 20 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
- Hazard
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 (4)
- t03312015@20
- t05062015@28
- t06082015@22
- t05112015@17.
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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