Key Pharmacy Recalls 5-MTHF Injections Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling 5-MTHF injections because the firm cannot assure the products are sterile.
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 sterility assurance failures are categorized as Severe.
Plain-English summary
Key Pharmacy and Compounding Center is recalling 100 vials of 5-MTHF 5mg/mL Injection, 10mL Glass/Multiple Dose vial. The product was distributed nationwide in the U.S.A., Australia, and Canada.
The recall was initiated due to a lack of assurance of sterility. The firm is recalling these sterile compounded drugs while they are within their expiration dates.
Consumers should stop using the affected product and contact their healthcare provider or the recalling firm for instructions on disposal or replacement.
The recalled product
- Product
- 5-MTHF *10ML* MDV 5MG/ML INJ, Injection, 5mg/mL, Rx only, 10mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
- Manufacturer
- Key Pharmacy and Compounding Center
- Category
- Drug — Compounded Sterile Drug
- Hazard
- Affected units
- 100
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 (8)
- Lot # t11-21-2016@112
- Exp 5/21/2017
- 12-15-2016@73
- Exp 6/13/2017
- 01-13-2017@67
- Exp 7/12/2017
- t02-14-2017@97
- Exp 8/14/2017
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 79 recalled by Key Pharmacy and Compounding Center 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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