Data Foundry

Medical device recalls 2022

VELYS Robotic-Assisted Solution Base Product No — Class II medical device recall Z-1029-2022

Terminated recall by DePuy Orthopaedics, Inc., reported 2022-05-11, distributed nationwide. System software v1.5.1 has a system software issue related to the Daylight Savings Time (DST) change that can

Recall numberZ-1029-2022
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmDePuy Orthopaedics, Inc., Warsaw, IN, United States
Recall initiated2022-03-11
Classified2022-05-02
Reported by FDA2022-05-11
Terminated2024-04-18
DistributedNationwide (US)
Countries outside the USAU, IL, NZ
Reason classessoftware
UPC / GTIN / UDI-DI10603295519515
Serial numbers10603295519515, BAS1004, BAS1009, BAS1022, BAS1052, BAS1054, BAS1060, BAS1061, BAS1062, BAS1063, BAS1066, BAS1068, BAS1069, BAS1070, BAS1071, BAS1073, BAS1076, BAS1078, BAS1079, BAS1081, BAS1082, BAS1093, BAS1111, BAS1118, BAS1119 and 44 more

Product

VELYS Robotic-Assisted Solution Base Product No.: 451570100

Reason for recall

System software v1.5.1 has a system software issue related to the Daylight Savings Time (DST) change that can cause a system error, requiring the user to restart the system and potentially cause a delay in treatment

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-1029-2022. 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.