Data Foundry

Drug recalls 2015

1% Lidocaine HCl Injection — Class II drug recall D-1815-2015

Ongoing recall by Hospira, Inc., reported 2015-09-30, distributed nationwide. Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of

Recall numberD-1815-2015
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmHospira, Inc., Lake Forest, IL, United States
Recall initiated2015-08-25
Classified2015-09-18
Reported by FDA2015-09-30
DistributedNationwide (US)
Quantity100,200 vials
Reason classesforeign material, specification failure
NDC00409-4275, 00409-4275-01, 00409-4275-16, 00409-4276, 00409-4276-01, 00409-4276-02, 00409-4276-16, 00409-4276-17, 00409-4277, 00409-4277-01, 00409-4277-02, 00409-4277-16, 00409-4277-17, 00409-4278, 00409-4278-01, 00409-4278-16, 00409-4279, 00409-4279-02, 00409-4279-16, 00409-4282, 00409-4282-01, 00409-4282-02, 00409-4282-11, 00409-4282-12, 00409-4282-25 and 14 more
Lot numbers44-359-DK
Expiration dates2016-08-01

Product

1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-4279-02

Reason for recall

Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.

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-1815-2015. 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.