FDA Device recall Z-0895-2018
Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400
- FDA Device
- Class II
- terminated
- Published 2018-03-14
On 2018-03-14 the FDA classified a Class II recall of Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400 by Instrumentation Laboratory, citing instrumentation Laboratory Co. received customer reports of performance issues with some vials of Lot Nos. N1166235 and N0177760, including increased imprecision, out of range qua….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0895-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-08-02 |
| Published | 2018-03-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Instrumentation Laboratory |
| Distribution | US |
Product
Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400
Reason
Instrumentation Laboratory Co. received customer reports of performance issues with some vials of Lot Nos. N1166235 and N0177760, including increased imprecision, out of range quality controls and prolonged sample results.
Identifiers
| code_info | Lots: N1166235, N0177760, N0278358, N0478057, N0479504 & N0278177. |
|---|
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-0895-2018%22
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