The Recall Desk
SevereFDA (Drugs)·D-1165-2015·Announced 2015-07-08

Lincare Recalls TPN 3:1 Bags Due to Sterility Concerns

Lincare, Inc. is recalling TPN 3:1 bags compounded in May 2015 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, which corresponds to a 'Severe' rating under the rubric for drug recalls involving potential serious health consequences.

Plain-English summary

Lincare, Inc. is recalling TPN 3:1, 1844 mL Bags (Qty: 6) compounded by United Medical IV Center in Little Rock, Arkansas. The recall involves all product compounded between May 14, 2015, and May 27, 2015.

The recall was initiated because the sterility of the product is not assured. The product is a prescription-only total parenteral nutrition (TPN) solution containing dextrose, amino acids, lipids, electrolytes, vitamins, and trace elements.

The affected product was distributed in the United States, including Arkansas. Patients who have received this product should contact their healthcare provider for further instructions.

The recalled product

Product
TPN 3:1, 1844 mL Bags, Qty: 6, Base Formula Sodium Chloride, Dextrose 70%, Clinisol SF 15%, Intralipid 20%, Water for Inj; Electrolytes KCL, Ca Gluconate, MgSO4, K Phos; Vitamins, trace elements and medications Multitrace-4, Multi Vitamin, Rx Only. Compounded by: United Medical I
Manufacturer
Lincare, Inc.
Category
Drug — Total Parenteral Nutrition
Hazard
Affected units
6

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 (3)

  • All product compounded between May 14
  • 2015 and May 27
  • 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.

See all 54 products in this recall →

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