Lincare Recalls Vancomycin Bags Due to Sterility Assurance Concerns
Lincare, Inc. is recalling 2 bags of Vancomycin 750 mg/NS 100 ml compounded by United Medical IV Center because the sterility of the product is not assured.
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 the hazard involves a lack of assurance of sterility in an intravenous medication, which poses a significant risk of serious injury or death if contaminated.
Plain-English summary
Lincare, Inc. is recalling 2 bags of Vancomycin 750 mg/NS 100 ml accuflo, packaged in 100 mL bags and marked as Rx Only. The product was compounded by United Medical IV Center in Little Rock, Arkansas, on May 29, 2015, with a discard after date of June 12, 2015.
The recall was initiated due to a lack of assurance of sterility, meaning the sterility of the product is not assured. The affected product was distributed in the United States, including Arkansas.
Consumers and healthcare providers should stop using the affected product and contact Lincare, Inc. or their healthcare provider for further instructions.
The recalled product
- Product
- Vancomycin 750 mg/NS 100 ml accuflo, Packaged in 100 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
- Manufacturer
- Lincare, Inc.
- Category
- Drug — Antibiotic
- 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 (2)
- Compounded on 05/29/2015
- Discard After: 06/12/2015
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 54 recalled by Lincare, Inc. 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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