D-1419-2012 Class I Terminated
FDA drug recall D-1419-2012 was initiated by Hospira Inc. on Apr 17, 2012 and is designated Class I. Reason for recall: Superpotent; Cartridges labeled to contain 1 mL found to contain 2.2 mL The recall status is terminated (terminated May 29, 2015). Affected quantity: 212,370 cartidges.
Recall Details
- Product Type
- Drugs
- Report Date
- Jul 25, 2012
- Initiation Date
- Apr 17, 2012
- Termination Date
- May 29, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 212,370 cartidges
Product Description
Morphine Sulfate Injection, USP, 4mg/mL, 1 mL fill in 2.5 mL Carpuject Cartridge Unit with Luer Lock, packaged 10 Carpujects/carton, CII, Rx only, Hospira, Inc., Lake Forest, IL ---- NDC 0409-1258-30
Reason for Recall
Superpotent; Cartridges labeled to contain 1 mL found to contain 2.2 mL
Distribution Pattern
Nationwide
Code Information
Lot #10830LL, Exp. 1APR2013
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-1419-2012
- openFDA file date
- Oct 27, 2026
- Loaded by RegDataLab
- Oct 29, 2026