FDA recall record

Hospira 0.9% Sodium Chloride Injection, USP 1000 mL Flexible Container recall — FDA D-1096-2014

Lack of Assurance of Sterility:Solution leaking through the port cover of the primary container, which was identified during a retain sample visual…

Class IIclassification
D-1096-2014official record ID
Mar 12, 2014report date

Recall record at a glance

Official recordD-1096-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHospira Inc.
Report dateMar 12, 2014
Recall initiation dateFeb 11, 2014
Quantity603,768 bags
LocationLake Forest, IL, United States

Official product description

0.9% Sodium Chloride Injection, USP 1000 mL Flexible Container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09

Why the product was recalled

Lack of Assurance of Sterility:Solution leaking through the port cover of the primary container, which was identified during a retain sample visual inspection.

Distribution information

Nationwide and Puerto Rico

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.