FDA Device recall Z-2165-2017
Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set Model Number(s): L7572
- FDA Device
- Class II
- terminated
- Published 2017-06-07
On 2017-06-07 the FDA classified a Class II recall of Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set Model Number(s): L7572 by Medtest Holdings, citing pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set stability claim is not being met.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2165-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2011-07-08 |
| Published | 2017-06-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medtest Holdings |
| Distribution | US |
Product
Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set Model Number(s): L7572. For the in vitro quantitative kinetic determination of lactate dehydrogenase activity in serum.
Reason
Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set stability claim is not being met.
Identifiers
| code_info | L7572 all configurations |
|---|
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-2165-2017%22
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