PlainRecalls
FDA Drug Moderate Class II Terminated

KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials repackaged individually inside an amber glass bottle, packaged by RemedyRepack, Indiana, PA, mfg by Hospira, Inc. Lake Forest, IL NDC 61786-0055-01

Reported: May 13, 2015 Initiated: April 23, 2015 #D-0974-2015

Product Description

KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials repackaged individually inside an amber glass bottle, packaged by RemedyRepack, Indiana, PA, mfg by Hospira, Inc. Lake Forest, IL NDC 61786-0055-01

Reason for Recall

Crystallization

Details

Recalling Firm
RemedyRepack Inc.
Units Affected
25
Distribution
PA and OK
Location
Indiana, PA

Frequently Asked Questions

What product was recalled?
KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials repackaged individually inside an amber glass bottle, packaged by RemedyRepack, Indiana, PA, mfg by Hospira, Inc. Lake Forest, IL NDC 61786-0055-01. Recalled by RemedyRepack Inc.. Units affected: 25.
Why was this product recalled?
Crystallization
Which agency issued this recall?
This recall was issued by the FDA Drug on May 13, 2015. Severity: Moderate. Recall number: D-0974-2015.