PlainRecalls
FDA Drug Moderate Class II Terminated

Ketorolac Tromethamine Inj. USP, 60 mg (30 mg/mL), 2 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL --- NDC 00409-3796-01 --- Also labeled under NOVAPLUS label NDC 00409-3796-49

Reported: May 6, 2015 Initiated: April 13, 2015 #D-0973-2015

Product Description

Ketorolac Tromethamine Inj. USP, 60 mg (30 mg/mL), 2 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL --- NDC 00409-3796-01 --- Also labeled under NOVAPLUS label NDC 00409-3796-49

Reason for Recall

Crystallization

Details

Recalling Firm
Hospira Inc.
Distribution
Nationwide, Puerto Rico and Guam.
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
Ketorolac Tromethamine Inj. USP, 60 mg (30 mg/mL), 2 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL --- NDC 00409-3796-01 --- Also labeled under NOVAPLUS label NDC 00409-3796-49. Recalled by Hospira Inc..
Why was this product recalled?
Crystallization
Which agency issued this recall?
This recall was issued by the FDA Drug on May 6, 2015. Severity: Moderate. Recall number: D-0973-2015.