The Recall Desk
Agency classClass IIOur severity:SevereFDA (Drugs)·D-1188-2015·Announced 2015-07-08

Lincare Recalls Vancomycin IV Bags Due to Sterility Concerns

Lincare, Inc. is recalling Vancomycin IV bags compounded by United Medical IV Center because the sterility of the product is not assured.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. 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 according to the rubric, particularly given the risk of infection from non-sterile IV products.

Plain-English summary

Lincare, Inc. is recalling Vancomycin 750mg / NS 100mL AccuFlo IV bags. The product was compounded by United Medical IV Center in Little Rock, Arkansas, and distributed in the United States, including Arkansas. The recall was initiated because the sterility of the product is not assured.

The affected product consists of 7 100 mL bags of Vancomycin 750mg / NS 100mL AccuFlo, which is a prescription-only medication. The specific lot was compounded on May 28, 2015, with a discard after date of June 11, 2015.

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, VANCOMYCIN 750mg / NS 100mL AccuFlo, Qty: 7 100 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 — IV Infusion
Hazard
Affected units
7

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 05/28/15
  • Discard After: 06/11/15

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.

See all 54 products in this recall →

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