DxM 1040 MicroScan WalkAway Instrument REF B1018-440 — Class II medical device recall Z-1085-2022
Ongoing recall by Beckman Coulter Inc., reported 2022-05-25, distributed nationwide. WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated a
| Recall number | Z-1085-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter Inc., Brea, CA, United States |
| Recall initiated | 2019-10-21 |
| Classified | 2022-05-13 |
| Reported by FDA | 2022-05-25 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, BE, BR, CH, CO, DE, ES, HK, ID, IT, JP, MX, PH, PL, PT, PY, RO, RU, SA, TW, VN |
| Quantity | 40 systems |
| UPC / GTIN / UDI-DI | 15099590690885 |
| Serial numbers | 44010026, 44010027, 44010028, 44010029, 44010030, 44010031, 44010032, 44010033, 44010035, 44010036, 44010037, 44010038, 44010040, 44010041, 44010042, 44010043, 44010044, 44010045, 44010046, 44010047, 44010048, 44010049, 44010050, 44010051, 44010052 and 15 more |
| Model numbers | B1018-440 |
Product
DxM 1040 MicroScan WalkAway Instrument REF B1018-440
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1085-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.