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.
Reported: March 26, 2014 Initiated: November 21, 2013 #D-1162-2014
Product Description
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.
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
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- 105,216 containers
- Distribution
- Nationwide, Puerto Rico, Singapore, Saudi Arabia and United Arab Emirates.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Baxter Healthcare Corp.. Units affected: 105,216 containers.
Why was this product recalled? ▼
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
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 26, 2014. Severity: Critical. Recall number: D-1162-2014.
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