Beckman Coulter MicroScan PROMPT Inoculation System-D — Class II medical device recall Z-1674-2020
Terminated recall by Beckman Coulter Inc., reported 2020-04-15, distributed nationwide. Due to customer reports it has been determined that the inoculation system contains the incorrect prompt wands
| Recall number | Z-1674-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter Inc., Brea, CA, United States |
| Recall initiated | 2019-12-13 |
| Classified | 2020-04-06 |
| Reported by FDA | 2020-04-15 |
| Terminated | 2021-04-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CN, JP, PY |
| Quantity | 3,472 units |
| UPC / GTIN / UDI-DI | 15099590659561 |
| Lot numbers | 20201103T |
| Model numbers | B1026-10D |
| Expiration dates | 2020-11-03 |
Product
Beckman Coulter MicroScan PROMPT Inoculation System-D, Catalog Number B1026-10D, UDI: 15099590659561 - Product Usage: The Prompt Inoculation System-D is used to standardize inocula for microdilution antimicrobial susceptibility test.
Reason for recall
Due to customer reports it has been determined that the inoculation system contains the incorrect prompt wands. Use of the incorrect wands could result in false -susceptible results, false-resistant results, possible misidentifications, or possible out-of-range Quality Control results.
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-1674-2020. 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.