Class II
Terminated
Heparin Sodium and 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL --- NDC 0338-0431-03
This recall has been terminated (originally issued June 17, 2015).
- Company
- Baxter Healthcare Corp.
- Recall Initiated
- June 3, 2015
- Posted
- June 17, 2015
- Recall Number
- D-1131-2015
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 145,350 containers
- Firm Location
- Deerfield, IL, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Subpotent Drug; out of specification results for heparin raw material
Distribution
Nationwide
Lot / Code Info
Product Code: 280953 Lots: N002998 and N003004 exp 12/31/15; and lot N003038 exp. 01/31/2016
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