CLASS III Drug recall · Reported 1 Oct 2014 · FDA Enforcement Report

Rifampin for Injection USP, 600 mg*/vial (Sterile) recalled by Akorn

Akorn is recalling Rifampin for Injection USP, 600 mg*/vial (Sterile), supplied in sterile glass vials, distributed nationwide in the US. The recall was initiated on 5 Aug 2014 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot: 12RIF4A, Expiration Date: 9/30/2014
Quantity recalled5,539 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-1571-2014
FDA event ID
69013
Recalling firm
Akorn, Lake Forest, IL
Classification
Class III
Status
Terminated
Recall initiated
5 Aug 2014
FDA classified
22 Sep 2014
Reported
1 Oct 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

5 Aug 2014Recall initiated by company
22 Sep 2014Classified by FDA+48 days
1 Oct 2014Published in enforcement report+9 days

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

Reason for recall

Failed Impurity/Degradation Specification; high out of specification result for 23 transacetyl impurity at the 22 month stability time point

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Rifampin for Injection USP, 600 mg*/vial (Sterile), supplied in sterile glass vials, Rx only For IV Infusion only, individually boxed, Mfd. for: Akorn, Inc., Lake Forest, IL --- NDC 17478-151-42

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Failed Impurity/Degradation Specification; high out of specification result for 23 transacetyl impurity at the 22 month stability time point

Which lots are affected?

Lot: 12RIF4A, Expiration Date: 9/30/2014

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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.

More recalls from Akorn

All 192

Other Rifampin recalls

All 21