Class II · Moderate risk Ongoing
Bicillin L-A
Reason CGMP Deviations; particulates identified during visual inspection
Penicillin G Potassium 5.4 MU/SW 240 mL AccuFlo
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
Penicillin G Potassium 5.4 MU/SW 240 mL AccuFlo, Qty: 4 240 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200 501-227-0900.
- Recalling firm
- Lincare, Inc.
- Origin
- AR, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1166-2015
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 Penicillin recalls
See all
Class I · High risk Ongoing
Buffered Penicillin G Potassium for Injection
Reason Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit
Class II · Moderate risk Terminated
Bicillin L-A
Reason cGMP Deviations: Products were stored outside the drug label specifications.
Class II · Moderate risk Terminated
Penicillin
Reason Lack of sterility assurance
Class II · Moderate risk Terminated
Penicillin V Potassium for Oral Solution
Reason Subpotent
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