CLASS I Drug recall · Reported 26 Mar 2014 · FDA Enforcement Report

Marcaine (bupivacaine HCl) injection recalled by Hospira

Hospira is recalling Marcaine (bupivacaine HCl) injection, USP, 0.25% single-dose vials-preservative free, distributed nationwide in the US. The recall was initiated on 18 Oct 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 25-220-DD, Exp 1JAN2015
NDC0409-0525, 0409-1559, 0409-1560, 0409-1582, 0409-1587, 0409-1610
Quantity recalled40,360 vials

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1161-2014
FDA event ID
66503
Recalling firm
Hospira, Lake Forest, IL
Manufacturer
Hospira, Inc.
Classification
Class I
Status
Terminated
Recall initiated
18 Oct 2013
FDA classified
14 Mar 2014
Reported
26 Mar 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Particulate Matter

Timeline

18 Oct 2013Recall initiated by company
14 Mar 2014Classified by FDA+147 days
26 Mar 2014Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.

Product as listed by the FDA

Marcaine (bupivacaine HCl) injection, USP, 0.25%, 30 mL single-dose vials-preservative free, packaged in 10-count vials per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1559-30.

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.

Which lots are affected?

Lot 25-220-DD, Exp 1JAN2015

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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