Reported May 6, 2015 · Terminated
Ketorolac Tromethamine Inj. USP, 30 mg (30 mg/mL), 1 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, 30 mg (30 mg/mL), 1 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL --- NDC 00409-3795-01--- Also labeled under NOVAPLUS label NDC 00409-3795-49
- Lot codes and dates
12 of 12 products
Products covered by this recall # Product as published 1 Lots 35-231-DK, 35-235-DK, 35-507-DK Exp. Date 1NOV2015 2 Lot 36-136-DK Exp. Date 1DEC2015 3 Lot 37-146-DK Exp. Date 1JAN2016 4 Lot 38-138-DK Exp. Date 1FEB2016 5 Lots 39-103-DK, 39-255-DK Exp. Date 1MAR2016 6 Lots 40-539-DK, 40-549-DK, Exp. Date 1APR2016 7 Lot 41-079-DK Exp. Date 1MAY2016 8 Lots 42-252-DK, 42-254-DK Exp. Date 1JUN2016 9 Lots 43-262-DK, 43-263-DK Exp. Date 1JUL2016 10 Lots 45-031-DK, 45-032-DK, 45-033-DK Exp. Date 1SEP2016 11 Lot 46-001-DK Exp. 1OCT2016 - Note: The lot number may be followed by additional numbers from 01 to 99 NOVAPLUS label Lot 35-230-DK Exp. Date 1NOV2015 12 Lot 40-535-DK Exp. Date 1APR2016 - Note: The 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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