Partell Specialty Pharmacy Recalls Lipoic Acid Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Lipoic Acid 25mg/mL vials in Nevada because the firm used a non-approved method of sterilization.
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, which corresponds to a Severe severity score under the rubric for significant injury or health risk potential.
Plain-English summary
Partell Specialty Pharmacy is recalling Lipoic Acid 25mg/mL, 5 mL amber vials, which are prescription-only products. The recall is being conducted because the firm used a non-approved method of sterilization, resulting in a lack of assurance of sterility for the drug products.
The affected products were distributed only in Nevada. Specific lot numbers and best-use dates are listed in the recall documentation, including lots 20180124@10, 20180220@9, and 20180102@33.
Consumers who have these specific vials should stop using them and contact their healthcare provider or pharmacist for further instructions.
The recalled product
- Product
- Lipoic Acid 25mg/mL, 5 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
- Manufacturer
- Partell Specialty Pharmacy
- Category
- Drug — Injectable
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 (6)
- Lot#: 20180124@10
- BUD 04/05/2018
- 20180220@9
- BUD 05/21/2018
- 20180102@33
- BUD 04/02/2018.
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 49 recalled by Partell Specialty 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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