FDA recall record

Lincare Ceftazidime 2 gm / NS 50mL, Qty: 15 50 mL Bags recall — FDA D-1201-2015

Lack of Assurance of Sterility: Sterility of product is not assured.

Class IIclassification
D-1201-2015official record ID
Jul 8, 2015report date

Recall record at a glance

Official recordD-1201-2015
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLincare, Inc.
Report dateJul 8, 2015
Recall initiation dateMay 28, 2015
Quantity15 Bags
LocationLittle Rock, AR, United States

Official product description

Ceftazidime 2 gm / NS 50mL, Qty: 15 50 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.

Why the product was recalled

Lack of Assurance of Sterility: Sterility of product is not assured.

Distribution information

United States including: Arkansas

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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