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.
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