Software 1898072 IPC upgrade v 2 — Class II medical device recall Z-2673-2020
Terminated recall by Medtronic Xomed, Inc., reported 2020-07-29, distributed nationwide. During internal testing execution of the next generation of Integrated Power Console (IPC) prototype it was no
| Recall number | Z-2673-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Xomed, Inc., Jacksonville, FL, United States |
| Recall initiated | 2020-06-12 |
| Classified | 2020-07-21 |
| Reported by FDA | 2020-07-29 |
| Terminated | 2023-04-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CA, CH, CN, DE, DK, ES, FI, FR, GB, GR, IT, JP, LU, NL, NO, NZ, PL, SE, SG |
| Quantity | 673 units |
| Lot numbers | 0217355465, 0217856852, 0217858947, 0217859045, 0218203285, 0218263964, 0218293282, 0218377490, 0218472653, 0218472654, 0218665536, 0218666231, 0218666243, 0218687534, 0218687535, 0218714701, 0218721203, 0218745073, 0218746389, 0218864105, 0218900337, 0218928638, 0218958034, 0218958035, 0219004569, 0219201122, 0219255151, 0219281168, 0219310085, 0219443322, 0219448447, 0219465587, 0219518520, 0219550550, 0219619754, 0219639840, 0219639842, 0219639844 |
| Model numbers | 1898072 |
Product
Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal, drilling and sawing of soft and hard tissue and bone in surgical procedures.
Reason for recall
During internal testing execution of the next generation of Integrated Power Console (IPC) prototype it was noted that the M5 Microdebrider was rotating at a higher speed than the set value in the cosole.
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-2673-2020. 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.