Data Foundry

Drug recalls 2013

Propofol Injectable Emulsion — Class II drug recall D-887-2013

Terminated recall by Hospira Inc., reported 2013-08-21, distributed nationwide. Presence of Particulate Matter; single visible particulate was identified during a retain sample inspection id

Recall numberD-887-2013
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmHospira Inc., Lake Forest, IL, United States
Recall initiated2013-05-25
Classified2013-08-13
Reported by FDA2013-08-21
Terminated2014-09-18
DistributedNationwide (US)
Quantity94,110 vials
Reason classesspecification failure
NDC00409-0010, 00409-0010-97, 00409-0010-98, 00409-0501, 00409-0501-97, 00409-0501-98, 00409-1511, 00409-1511-97, 00409-1511-98, 00409-4699, 00409-4699-24, 00409-4699-30, 00409-4699-33, 00409-4699-50, 00409-4699-53, 00409-4699-54, 00409-6010, 00409-6010-02, 00409-6010-25
Lot numbers07-950-DJ, 10-101-DJ, 10-102-DJ
Expiration dates2013-07-01, 2013-10-01

Product

Propofol Injectable Emulsion, 1%, 1 g/100 mL (10 mg/mL), 100 mL, Single patient infusion vial, RX only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-24; Propofol Injectable Emulsion, 500 mg/50 mL, 50 mL, Single patient infusion vial, RX only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-33

Reason for recall

Presence of Particulate Matter; single visible particulate was identified during a retain sample inspection identified as stainless steel

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-887-2013. 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.