0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.

FDA recall notice · announced May 13, 2015 · Hospira

Class I FDA/FSIS Class I: reasonable probability that use will cause serious adverse health consequences or death.

The product

0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.

Reason for recall

Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.

Notes

Distribution: Nationwide.
Lot/code information: Lot # 45-110-C6; Exp 03/1/16
Quantity: 9,912 VisIV flex containers
Status: Terminated
Products in this recall event:
- 0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25. (D-0976-2015)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.