FDA Drug recall D-1444-2012
HYDROmorphone HCl Injection, USP, 1 mg/mL, 1 mL fill in a 2.5 mL Carpuject prefilled cartridge unit, packaged in 10-count Carpujects per ca…
- FDA Drug
- Class I
- terminated
- Published 2012-08-15
On 2012-08-15 the FDA classified a Class I recall of HYDROmorphone HCl Injection, USP, 1 mg/mL, 1 mL fill in a 2.5 mL Carpuject prefilled cartridge unit, packaged in 10-count Carpujects per ca… by Hospira, citing superpotent (Single Ingredient) Drug: Some of the prefilled cartridge units have been found to be overfilled and contain more than the 1 mL labeled fill volume.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1444-2012 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-05-12 |
| Published | 2012-08-15 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
Product
HYDROmorphone HCl Injection, USP, 1 mg/mL, 1 mL fill in a 2.5 mL Carpuject prefilled cartridge unit, packaged in 10-count Carpujects per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1283-31, Barcode (01) 1 030409 128331 9 (carton), (01) 0 030409 128331 2 (cartridge unit).
Reason
Superpotent (Single Ingredient) Drug: Some of the prefilled cartridge units have been found to be overfilled and contain more than the 1 mL labeled fill volume.
Identifiers
| ndc | 0409-2552-11 |
|---|---|
| ndc | 0409-2552-01 |
| ndc | 0409-3356-11 |
| ndc | 0409-3356-01 |
| ndc | 0409-2540-11 |
| ndc | 0409-2540-01 |
| ndc | 0409-3365-11 |
| ndc | 0409-3365-01 |
| ndc | 0409-3365-10 |
| ndc | 0409-1283-03 |
| ndc | 0409-1283-31 |
| ndc | 0409-1312-03 |
| ndc | 0409-1312-30 |
| ndc | 0409-1304-03 |
| ndc | 0409-1304-31 |
| code_info | Lot #07547LL, Exp 07/01/13 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1444-2012%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.