FDA Device recall Z-1671-2016
AB Sciex Triple Quad 4500MD LC/MS/MS System, Part No. 5031257
- FDA Device
- Class II
- terminated
- Published 2016-05-25
On 2016-05-25 the FDA classified a Class II recall of AB Sciex Triple Quad 4500MD LC/MS/MS System, Part No. 5031257 by Ab Sciex, citing under certain conditions, mass spectrometers may report incorrect quantitative results.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1671-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-03-25 |
| Published | 2016-05-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ab Sciex |
| Distribution | NC |
Product
AB Sciex Triple Quad 4500MD LC/MS/MS System, Part No. 5031257; and QTRAP 4500MD LC/MS/MS System, Part No. 5031231. Mass spectrometers for in vitro diagnostic use only.
Reason
Under certain conditions, mass spectrometers may report incorrect quantitative results.
Identifiers
| code_info | Serial Numbers: Triple Quad 4500MD LC/MS/MS System BX21081601 BX21101601 BX21091601 BX21111601 BX21121602 BX21…Serial Numbers: Triple Quad 4500MD LC/MS/MS System BX21081601 BX21101601 BX21091601 BX21111601 BX21121602 BX21131602 BX21141602 BX21151602 QTRAP 4500MD LC/MS/MS System BW20251601 BW20241601 BW20261602 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1671-2016%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.