The Vesa 75/100 adaptation with rotation is an accessory to a… — Class II medical device recall Z-1188-2016
Terminated recall by Richard Wolf Medical Instruments Corp., reported 2016-03-23, distributed nationwide. Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of their monitor mounts and support ar
| Recall number | Z-1188-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Richard Wolf Medical Instruments Corp., Vernon Hills, IL, United States |
| Recall initiated | 2016-02-29 |
| Classified | 2016-03-17 |
| Reported by FDA | 2016-03-23 |
| Terminated | 2019-07-03 |
| Distributed | Nationwide (US) |
| Quantity | 108 units |
| Serial numbers | 001X001107, 001X001108, 001X001109, 001X001110, 001X001111, 001X001142, 001X001143, 001X001144, 001X001145, 001X001146, 001X001147, 001X001148, 001X001149, 001X001150, 001X001151, 001X001168, 001X001169, 001X001170, 001X001171, 001X001172, 001X001173, 001X001174, 001X001175, 001X001176, 001X001177 and 120 more |
Product
The Vesa 75/100 adaptation with rotation is an accessory to a surgical camera intended to be used to record operative procedures.
Reason for recall
Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of their monitor mounts and support arms may be missing riveting.
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-1188-2016. 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.