Home/Recalls/FDA-D-0429-2026
FDA DrugsClass II

0.9% Sodium Chloride Injection, USP, 50 mL x60, Becton, Dickson and Company, 1 B...

Published: April 15, 2026Recall ID: D-0429-2026Category: drugsCountry: US

Reason for Recall / Hazard

Lack of Assurance of Sterility

Product Description & Identification

0.9% Sodium Chloride Injection, USP, 50 mL x60, Becton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417 USA, Distributed by BD, Manufactured by Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Sale NDC Number: 17271-701-02.

Additional Source Details

FieldValue
CityLake Zurich
StateIL
Openfda › Unii451W47IQ8X
Openfda › RouteINTRAVENOUS
Openfda › Rxcui › 11807631
Openfda › Rxcui › 21807632
Openfda › Rxcui › 31807633
Openfda › Rxcui › 41807634
Openfda › Rxcui › 51807639
Openfda › Spl id31344de2-e115-440a-a913-ff63da5f17d8
Openfda › Brand nameSODIUM CHLORIDE
Openfda › Spl set idebc8b008-a8b3-4c41-89e4-b413f7aab89f
Openfda › Package ndc › 117271-701-02
Openfda › Package ndc › 217271-701-03
Openfda › Package ndc › 317271-701-05
Openfda › Package ndc › 417271-701-06
Openfda › Package ndc › 517271-701-07
Openfda › Product ndc17271-701
Openfda › Generic nameSODIUM CHLORIDE
Openfda › Product typeHUMAN PRESCRIPTION DRUG
Openfda › Substance nameSODIUM CHLORIDE
Openfda › Manufacturer nameBecton Dickinson and Company
Openfda › Application numberANDA207310
Openfda › Is original packagertrue
Event id98581
Address 13 Corporate Dr
Code infoBatch# 6402428, Exp Date: 10/31/2026; Batch# 6402481, 6402482, Exp Date: 11/30/2026.
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