FDA Device recall Z-1084-2022
MicroScan WalkAway-96 plus Instrument REF B1018-284
- FDA Device
- Class II
- ongoing
- Published 2022-05-25
On 2022-05-25 the FDA classified a Class II recall of MicroScan WalkAway-96 plus Instrument REF B1018-284 by Beckman Coulter, citing walkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 1….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1084-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-10-21 |
| Published | 2022-05-25 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Beckman Coulter |
| Distribution | US |
Product
MicroScan WalkAway-96 plus Instrument REF B1018-284
Reason
WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10 ampere
Identifiers
| code_info | Catalog Number: B1018-284 UDI-DI Code: 15099590658687 Serial Numbers: 39610007 39610008 39610009 39610010 39610011 39610012 39610013 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1084-2022%22
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