D-0976-2015 Class I Terminated
FDA drug recall D-0976-2015 was initiated by Hospira Inc. on Mar 5, 2015 and is designated Class I. Reason for recall: Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution. The recall status is terminated (terminated Jun 9, 2016). Affected quantity: 9,912 VisIV flex containers.
Recall Details
- Product Type
- Drugs
- Report Date
- May 13, 2015
- Initiation Date
- Mar 5, 2015
- Termination Date
- Jun 9, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9,912 VisIV flex containers
Product Description
0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.
Reason for Recall
Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.
Distribution Pattern
Nationwide.
Code Information
Lot # 45-110-C6; Exp 03/1/16
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0976-2015
- openFDA file date
- Oct 27, 2026
- Loaded by RegDataLab
- Oct 29, 2026