Key Pharmacy Recalls Sterile Compounded Injection Due to Sterility Concerns
Key Pharmacy and Compounding Center is recalling TRI MIX 45.45/27.27/0.45 5ML MDV MCG/MG/MG/ML INJ due to 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 sterile compounded drug with a lack of assurance of sterility, which poses a risk of serious health consequences such as infection.
Plain-English summary
Key Pharmacy and Compounding Center is recalling a specific lot of TRI MIX 45.45/27.27/0.45 5ML MDV MCG/MG/MG/ML INJ. This is a prescription-only sterile compounded drug available in 5 mL glass multiple-dose vials. The recall is being conducted because the firm lacks assurance of the sterility of the product.
The affected product is identified by Lot # t12-12-2016@87 and has an expiration date of 5/22/2017. The source text indicates that this product was distributed nationwide in the U.S.A., as well as in Australia and Canada.
Consumers and healthcare providers should stop using the affected product and contact their healthcare provider or the recalling firm for further instructions. The FDA has classified this recall as Class II.
The recalled product
- Product
- TRI MIX 45.45/27.27/0.45 5ML MDV MCG/MG/MG/ML INJ, Injection, 45.45mcg/27.27mg/0.45mg/mL, Rx only, 5 mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
- Manufacturer
- Key Pharmacy and Compounding Center
- Category
- Drug — Compounded Sterile Drug
- Affected units
- 1
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 (2)
- Lot # t12-12-2016@87
- Exp 5/22/2017
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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