CLASS II Drug recall · Reported 8 Jan 2014 · FDA Enforcement Report

0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj. recalled by Hospira

Hospira is recalling 0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj., Multiple-dose Fliptop Vial, distributed nationwide in the US. The recall was initiated on 11 Oct 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #32-484-EV, 32-485-EV Exp: 2/2015.
NDC0409-1159, 0409-1160, 0409-1162, 0409-1163, 0409-1165, 0409-9043
Quantity recalled65109 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-395-2014
FDA event ID
67045
Recalling firm
Hospira, Lake Forest, IL
Manufacturer
Hospira, Inc.
Classification
Class II
Status
Terminated
Recall initiated
11 Oct 2013
FDA classified
2 Jan 2014
Reported
8 Jan 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

11 Oct 2013Recall initiated by company
2 Jan 2014Classified by FDA+83 days
8 Jan 2014Published in enforcement report+6 days

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

Reason for recall

Lack of assurance of sterility; equipment failure led to potential breach in asceptic process.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj., 50 mL, Multiple-dose Fliptop Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045. NDC #0409-9046-01.

Where it was distributed

US Nationwide.

Nationwide

Questions about this recall

Why was it recalled?

Lack of assurance of sterility; equipment failure led to potential breach in asceptic process.

Which lots are affected?

Lot #32-484-EV, 32-485-EV Exp: 2/2015.

Where was it sold?

US 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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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