Moses Lake Pharmacy Recalls Medroxyprogesterone Acetate Syringes Due to Sterility Concerns
Moses Lake Professional Pharmacy is recalling 11 syringes of Medroxyprogesterone Acetate because the FDA determined there is 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 FDA classified this recall as Class II. According to the rubric, an FDA Class II recall involving a sterile injectable drug where sterility is not assured is categorized as Severe (Score 4) due to the potential for significant injury or infection.
Plain-English summary
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 11 syringes of Medroxyprogesterone Acetate, 150mg/mL, 10mL. The recall was initiated because the U.S. Food and Drug Administration determined there is a lack of assurance of sterility for the product.
The affected product is a prescription-only injectable solution. The recall covers specific lots identified by the codes t03182015@4 and t07062015@5. The distribution pattern for these products is listed as nationwide.
Consumers who have this product should stop using it and contact their healthcare provider or the pharmacy for further instructions. 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.
The recalled product
- Product
- MEDROXYPROGESTERONE ACETATE, injectable Solution,150MG/ML, 10mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
- Category
- Drug — Injectable Sterile
- Affected units
- 11
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)
- t03182015@4 and t07062015@5
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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