D-836-2013 Class I Terminated
FDA drug recall D-836-2013 was initiated by Hospira Inc. on Mar 29, 2013 and is designated Class I. Reason for recall: Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates The recall status is terminated (terminated Jul 20, 2015). Affected quantity: 691,356 containers.
Recall Details
- Product Type
- Drugs
- Report Date
- Aug 14, 2013
- Initiation Date
- Mar 29, 2013
- Termination Date
- Jul 20, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 691,356 containers
Product Description
0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
Reason for Recall
Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates
Distribution Pattern
Nationwide
Code Information
Lot #: 25-037-JT*, Exp 1JAN2015, Note: the lot number may be followed by 01 or 90
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-836-2013
- openFDA file date
- Oct 27, 2026
- Loaded by RegDataLab
- Oct 29, 2026