Power Processor 3K — Class II medical device recall Z-0117-2022
Ongoing recall by Beckman Coulter Inc., reported 2021-10-20, distributed nationwide. Missing splash guard which may expose users to hazardous materials. .
| Recall number | Z-0117-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter Inc., Brea, CA, United States |
| Recall initiated | 2021-07-28 |
| Classified | 2021-10-14 |
| Reported by FDA | 2021-10-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CN, ES, FR, GB, IL, IT, KR, KW, LB, MX, MY, NL, PT, QA, SA, TH, TR, TW, ZA |
| UPC / GTIN / UDI-DI | 15099590591960 |
| Serial numbers | 90AM06007008, 90AM060703, 90AM060704, 90AM0710002, 90AM0710004, 90AM0710008, 90AM0711004, 90AM0711005, 90AM0801003, 90AM0801004, 90AM0802002, 90AM0803001, 90AM0803002, 90AM0805001, 90AM0806003, 90AM0808002, 90AM0810001, 90AM0901002, 90AM0902005, 90AM0902009, 90AM0903002, 90AM0904004, 90AM0904005, 90AM0905006, 90AM0905007 and 56 more |
| Model numbers | 6915556, A88116 |
Product
Power Processor 3K, 3K High Speed Stockyards Module Nameplate: PP 3K Stockyard (Refrig) 9707 REF A88116
Reason for recall
Missing splash guard which may expose users to hazardous materials. .
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-0117-2022. 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.