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.
Check against the official notice below — it lists the full affected range.
Baxter Healthcare Corp. is voluntarily recalling 5% Dextrose Injection, USP in 100 mL VIAFLEX plastic containers (Product code 2B0089, NDC 0338-0017-) due to the presence of particulate matter found in the solution. The contamination includes polyester and cotton fibers, adhesive-like mixture, polyacetal particles, thermally degraded PVC, black polypropylene, and human hair embedded in the plastic bags. The recall affects 105,216 containers of Lot #P285288 with expiration date 11/13, distributed nationwide as well as in Puerto Rico, Singapore, Saudi Arabia, and United Arab Emirates.
The source document does not specify a remedy or instructions for what affected consumers should do regarding this recall.
Written by software from the official notice below. Not reviewed by a lawyer.
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
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. Quantity: 105,216 containers Lot/code info: Lot #: P285288, Exp 11/13
Official record: FDA (Drug enforcement) ↗
Republished from the official source above; details can change — the source record controls.