0.9% Sodium Chloride Injection USP, 100 mL Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7984-23,

FDA recall notice · announced March 13, 2013 · Hospira

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The product

0.9% Sodium Chloride Injection USP, 100 mL Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7984-23,

Reason for recall

Lack of Assurance of Sterility: There is the potential for solution to leak from the administrative port to the fill tube seal.

Notes

Distribution: Nationwide
Lot/code information: Lot Number 02-117-JT Exp. 02/13
Quantity: 325,056 bags
Status: Terminated
Products in this recall event:
- 0.9% Sodium Chloride Injection USP, 100 mL Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7984-23, (D-183-2013)

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