Data Foundry

Drug recalls 2017

Norepinephrine Bitartrate 8 mg added to 0 — Class II drug recall D-0022-2018

Terminated recall by Banner Pharmacy Services, LLC, reported 2017-11-01, distributed nationwide. Lack of Assurance of Sterility.

Recall numberD-0022-2018
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBanner Pharmacy Services, LLC, Chandler, AZ, United States
Recall initiated2017-10-10
Classified2017-10-23
Reported by FDA2017-11-01
Terminated2018-08-09
DistributedNationwide (US)
Quantity3,550 bags
Reason classessterility
Lot numbers071217S2, 071417S1, 071917S2, 071917S3, 072117S1, 072617S2, 072617S3, 072817S2, 073117S2, 080217S2, 080717S2, 081117S2, 081417S2, 081617S2, 082217S2, 082317S2, 082917S2
Expiration dates2017-10-11, 2017-10-13, 2017-10-18, 2017-10-20, 2017-10-25, 2017-10-27, 2017-11-01, 2017-11-06, 2017-11-10, 2017-11-13, 2017-11-15, 2017-11-21, 2017-11-22, 2019-11-28

Product

Norepinephrine Bitartrate 8 mg added to 0.9% Sodium Chloride 250 mL in a bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025011501

Reason for recall

Lack of Assurance of Sterility.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0022-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.