Partell Specialty Pharmacy Recalls Nandrolone Decanoate Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Nandrolone decanoate 200mg/mL vials because they were sterilized using a non-approved method.
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 agency classified this as an FDA Class II recall. Per the rubric, FDA Class II recalls involving significant risks such as lack of sterility assurance are categorized as Severe.
Plain-English summary
Partell Specialty Pharmacy is recalling Nandrolone decanoate 200mg/mL, 5 mL amber vials. The recall is being conducted because the firm used a non-approved method of sterilization for these drug products.
The affected products are prescription-only and were distributed only in Nevada. The recall includes two vials with lot numbers 20180221@15 (expiration date 05/22/2018) and 20180123@10 (expiration date 04/23/2018).
Consumers who have these specific vials should stop using them and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- Nandrolone decanoate 200mg/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 Steroids
- Hazard
- Affected units
- 2
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)
- Lot#: 20180221@15
- BUD 05/22/2018
- 20180123@10
- BUD 04/23/2018.
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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