US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 28, 2015 (11 years ago)

VANCOMYCIN HCL 250mg / NS 6mL syringe

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

VANCOMYCIN HCL 250mg / NS 6mL syringe, Packaged in 6 mL Syringes, 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-1181-2015

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 Vancomycin recalls

See all
Class II · Moderate risk Ongoing

Vancomycin HCL

Reason Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

Fagron Compounding Services NDC 71266-5082-01 D-0442-2026
Class II · Moderate risk Ongoing

Vancomycin HCI

Reason Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

Fagron Compounding Services NDC 71266-5085-01 D-0441-2026
Class II · Moderate risk Ongoing

Vancomycin HCI

Reason Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

Fagron Compounding Services NDC 71266-5083-01 D-0440-2026
Class II · Moderate risk Ongoing

vancomycin HCl

Reason Lack of Assurance of Sterility

Fresenius Kabi Compounding, LLC NDC 71506-019-59 D-0337-2026
Class II · Moderate risk Ongoing

vancomycin HCl

Reason Lack of Assurance of Sterility

Fresenius Kabi Compounding, LLC NDC 71506-016-59 D-0336-2026