Class I
Terminated
5% Dextrose Injection, USP, 100 mL Single dose VIAFLEX plastic containers, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product code 2B0089, NDC 0338-0017-38.
This recall has been terminated (originally issued March 26, 2014).
- Company
- Baxter Healthcare Corp.
- Recall Initiated
- November 21, 2013
- Posted
- March 26, 2014
- Recall Number
- D-1162-2014
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 105,216 containers
- Firm Location
- Deerfield, IL, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Presence of Paticulate Matter; Baxter is issuing a voluntary recall for these IV solutions due to particulate matter found in the solution identified as polyester and cotton fibers, adhesive-like mixture, polyacetal particles, thermally degraded PVC, black polypropylene and human hair embedded in the plastic bag
Distribution
Nationwide, Puerto Rico, Singapore, Saudi Arabia and United Arab Emirates.
Lot / Code Info
Lot #: P285288, Exp 11/13
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