Home/Recalls/FDA-D-0433-2026
FDA DrugsClass II

0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 1,000 mL in...

Published: April 15, 2026Recall ID: D-0433-2026Category: drugsCountry: US

Reason for Recall / Hazard

Lack of Assurance of Sterility

Product Description & Identification

0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 1,000 mL in a Single Dose freeflex bag, 1,000 mLx10, Fresenius Medical Care, Waltham, MA 02451, Distributed by: Fresenius Medical Care RTG, LLC, Manufactured by: Fresenius Kabi, Unit of Use NDC: 65219-282-01, Unit of Sale NDC Number: 65219-282-10.

Additional Source Details

FieldValue
CityLake Zurich
StateIL
Openfda › Unii451W47IQ8X
Openfda › RouteINTRAVENOUS
Openfda › Rxcui1807639
Openfda › Spl id2ad355c8-4420-42d5-8ea8-b4cc3ccc1c0e
Openfda › Brand nameSODIUM CHLORIDE
Openfda › Spl set id6d43fa91-0940-437f-ba70-b2d3f977593e
Openfda › Package ndc › 165219-282-01
Openfda › Package ndc › 265219-282-10
Openfda › Product ndc65219-282
Openfda › Generic nameSODIUM CHLORIDE
Openfda › Product typeHUMAN PRESCRIPTION DRUG
Openfda › Substance nameSODIUM CHLORIDE
Openfda › Manufacturer nameFresenius Kabi USA, LLC
Openfda › Application numberANDA207310
Openfda › Is original packagertrue
Event id98581
Address 13 Corporate Dr
Code infoBatch# 23SU10001, Exp Date: 12/31/2026; Batch# 24AU10003, 24AU10004, 24AU10005, 24AU10008, Exp Date: 01/31/2027; Batch # 24EU10001, 24EU10002, Exp Date: 05/31/2027; Batch# 24PU10002, Exp Date: 11/30/2027; Batch# 25BU10003, Exp Date: 02/29/2028; Batch# 25EU10005, Exp Date: 05/31/2028.
Postal code60047-8930
Report date20260415
Product typeDrugs
Reason for recallLack of Assurance of Sterility
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260311
Initial firm notificationLetter
Center classification date20260403

Overview

  • Recalling FirmFresenius Kabi USA, LLC
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide , Alaska, and Puerto Rico.
Official Agency Alert