Reported May 6, 2015 · Terminated
Ketorolac Tromethamine Inj. USP, 60 mg (30 mg/mL), 2 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL…
Hospira Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hospira Inc. · 600 N Field Dr · Lake Forest, IL · 60045-4835
Is this the product you have?
- 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
- Lot codes and dates
3 of 3 products
Products covered by this recall # Product as published 1 lot number may be followed by additional numbers from 01 to 99 NOVAPLUS label 2 Lot 38-137-DK Exp. Date 1FEB2016 - Note: The 3 lot number may be followed by additional numbers from 01 to 99
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Crystallization
This product could cause temporary or reversible health problems — stop using it.
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