FDA Device recall Z-1387-2014
Morphine Test Card (2000)
- FDA Device
- Class II
- terminated
- Published 2014-04-16
On 2014-04-16 the FDA classified a Class II recall of Morphine Test Card (2000) by Lumiquick Diagnostics, citing products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1387-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-03-04 |
| Published | 2014-04-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Lumiquick Diagnostics |
| Distribution | CA, FL, NJ, NY, TX |
Product
Morphine Test Card (2000); LumiQuick, Santa Clara, CA 95054
Reason
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Identifiers
| code_info | Catalog number: 74032, All lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1387-2014%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.