Class II · Moderate risk Terminated
Endophth Kit
Reason Lack of Assurance of Sterility
Ceftazidime 2 gm / NS 50mL
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility: Sterility of product is not assured.
What was recalled
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.
- Recalling firm
- Lincare, Inc.
- Origin
- AR, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1201-2015
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Ceftazidime recalls
See all
Class II · Moderate risk Terminated
Ceftazidime Intravitreal
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Class II · Moderate risk Ongoing
CEFTAZIDIME INTRAVITREAL 2.25MG/0.1ML Solution
Reason Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class II · Moderate risk Terminated
Ceftazidime
Reason Lack of Assurance of Sterility
Class I · High risk Terminated
Ceftazidime for Injection USP and Dextrose for Injection USP
Reason Failed Stability Specifications: Out-of-Specification (OOS) results for High Molecular Weight Polymers.
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