FDA recall record

Bupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25% recall — FDA D-0218-2017

Presence of particulate matter: Confirmed customer report for the presence of particulate matter within a single vial.

Class Iclassification
D-0218-2017official record ID
Dec 28, 2016report date

Recall record at a glance

Official recordD-0218-2017
CategoryDrug Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmHospira Inc., A Pfizer Company
Report dateDec 28, 2016
Recall initiation dateAug 4, 2016
Quantity143,250 vials
LocationLake Forest, IL, United States

Official product description

Bupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25%, packaged in 30 mL Single-dose Preservative-Free vials, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1159-02

Why the product was recalled

Presence of particulate matter: Confirmed customer report for the presence of particulate matter within a single vial.

Distribution information

Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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