RecallRadar

FDA Drug recall D-0941-2018

Vancomycin 1.25gm in D5W 250 mL. ( Vancomycin HCL (USP) 1.25 gm, 5% Dextrose Inj. (USP) 250 mL) Volume: 262 mL. Single dose bag

On 2018-07-25 the FDA classified a Class II recall of Vancomycin 1.25gm in D5W 250 mL. ( Vancomycin HCL (USP) 1.25 gm, 5% Dextrose Inj. (USP) 250 mL) Volume: 262 mL. Single dose bag by Avella Of Deer Valley Store 38, citing lack of Assurance of Sterility: Potential leakage of bags.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0941-2018
ClassificationClass II
Statusterminated
Initiated2018-06-12
Published2018-07-25
Last updated2026-09-13 11:52 UTC
CompanyAvella Of Deer Valley Store 38
DistributionUS

Product

Vancomycin 1.25gm in D5W 250 mL. ( Vancomycin HCL (USP) 1.25 gm, 5% Dextrose Inj. (USP) 250 mL) Volume: 262 mL. Single dose bag. Avella Specialty Pharmacy, 24416N 19th Avenue, Phoenix, AZ 85085. NDC 42852-617-25

Reason

Lack of Assurance of Sterility: Potential leakage of bags.

Identifiers

code_infoLot # 138-20181005@92, 138-20181005@91, 138-20181005@90, BUD 7/9/2018; 138-20181405@78, BUD 7/13/2018; 138-20181605@61, BUD 7/15/2018

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0941-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.