Uroskop Omnia max — Class II medical device recall Z-1333-2020
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2020-02-26, distributed nationwide. Siemens became aware of an issue of incorrect use of the bypass key overriding the built-in collision control
| Recall number | Z-1333-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2020-01-08 |
| Classified | 2020-02-20 |
| Reported by FDA | 2020-02-26 |
| Terminated | 2022-06-21 |
| Distributed | Nationwide (US) |
| Quantity | 192 |
| Serial numbers | 4014, 4015, 4020, 4022, 4024, 4025, 4032, 4033, 4036, 4037, 4042, 4043, 4047, 4049, 4051, 4052, 4053, 4054, 4055, 4056, 4059, 4060, 4061, 4062, 4063 and 167 more |
| Model numbers | 10762473 |
Product
Uroskop Omnia max, Model No. 10762473 - Product Usage: Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system is designed primarily for urological diagnosis and the support of urological therapeutic applications such as examinations and small interventions of the urogenital tract.
Reason for recall
Siemens became aware of an issue of incorrect use of the bypass key overriding the built-in collision control creating risk of collision with obstacles or persons when the operator uses the override function.
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-1333-2020. 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.