Partell Specialty Pharmacy Recalls Biotin Suspension Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Biotin Suspension 10mg/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 recall is classified as FDA Class II, which corresponds to a Severe severity score under the rubric for significant injury or property damage reports or high-risk scenarios.
Plain-English summary
Partell Specialty Pharmacy is recalling Biotin Suspension 10mg/mL, 5 mL amber vials. The recall is being conducted because the firm used a non-approved method of sterilization for the drug products.
The affected products are prescription-only and were distributed in Nevada. The specific lots involved are 20180216@10 with a beyond-use date of 5/17/2018, and 20180129@25 with a beyond-use date of 04/29/2018.
Consumers who have these products should stop using them and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- Biotin Suspension 10mg/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 — Pharmacy Compounded
- 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 #:20180216@10
- BUD 5/17/2018
- 20180129@25
- BUD 04/29/2018.
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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