Moses Lake Pharmacy Recalls Alprostadil/Procaine Injectable Solution for Sterility Concerns
JD & SN Inc. is recalling 150 vials of Alprostadil/Procaine 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., dba Moses Lake Professional Pharmacy, is recalling 150 vials of Alprostadil/Procaine, Injectable Solution, 20 MCG/0.1%/ML, 10 mL vial. The recall was initiated because of a lack of assurance of sterility for all sterile human compounded drugs within their expiry dates.
The affected product is prescription-only and was distributed nationwide. The recall covers specific lots with expiration dates ranging from 2014 to 2015, including codes such as 01122015@4, 02022015@2, and t03062015@44.
Consumers and healthcare providers should stop using the recalled product and contact the pharmacy or their healthcare provider for further instructions.
The recalled product
- Product
- ALPROSTADIL/PROCAINE, Injectable Solution, 20 MCG/0.1%/ML, 10 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 — Injectable Solution
- Affected units
- 150
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 (20)
- 01122015@4
- 02022015@2
- 02102015@29
- 02202015@14
- 03302015@9
- 04132015@7
- 04222015@4
- 05062015@6
- 05132015@2
- 05272015@11
- 06032015@1
- 06102015@6
- 06222015@9
- 06232014@2
- 07082015@4
- 07112014@22
- 07292014@33
- 08182014@8
- 09022014@5
- 09092014@27
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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