November 2022 FDA Recall Sodium Chloride by Fresenius Medical Care Holdings, Inc.
D-0075-2023 - Lack of Assurance of Sterility

This Class II drug recall was voluntarily initiated by Fresenius Medical Care Holdings, Inc. on November 22, 2022 for the product Sodium Chloride. The FDA reported the reason for recall as lack of assurance of sterility. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0075-2023

Reason for Recall
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Initiated
11-22-2022
Reported
12-14-2022
Quantity
4,097 cases/12 bags per case

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Fresenius Medical Care Holdings, Inc.
Product was distributed Nationwide in the USA.
0.9% Sodium Chloride Injection, USP, Each 100 mL contains: SODIUM CHLORIDE, USP - 900 mg, WATER FOR INJECTION, USP - qs, 1000mL Bag, 12 PK, Rx Only, Fresenius Medical Care North America, Waltham, MA 02451, NDC 49230-300-10

Batch or Lot Expiration Information

Lot# 22HU05062, 22HU06059, 22HU05035, EXP 06/30/2023; 22JU05001, EXP 07/31/2023

Affected Packages Involved in this Recall