The Stryker Visum¿ LED Surgical Lighting system is intended to… — Class II medical device recall Z-1699-2017
Terminated recall by Stryker Communications, reported 2017-04-05, distributed nationwide. The potential hazard that can arise for the combination of the missing screws and the overloading by the end u
| Recall number | Z-1699-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Communications, Flower Mound, TX, United States |
| Recall initiated | 2017-02-28 |
| Classified | 2017-03-29 |
| Reported by FDA | 2017-04-05 |
| Terminated | 2018-01-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, GB, JP, NL |
| Quantity | 292 devices |
| Serial numbers | 100000000086360, 100000000087549, 100000000087555, 100000000088303, 100000000089194, 100000000089467, 100000000089970, 100000000090520, 100000000090522, 100000000090530, 100000000091032, 100000000091531, 100000000091728, 100000000091762, 100000000091766, 100000000091778, 100000000092672, 100000000092699, 100000000093927, 100000000093928, 100000000093936, 100000000093937, 100000000093938, 100000000093939, 100000000094391 and 33 more |
| Model numbers | 0682001432 |
Product
The Stryker Visum¿ LED Surgical Lighting system is intended to illuminate the operative site during surgical procedures with high intensity light. Affected part numbers are 0682001432 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 9P/FP), 0682001286 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 5P/FP), 0682001298 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 5P), 0682001299 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 5P/5P), 0682001300 (EDS LIGHT SUSPENSION, CENTRAL AXIS, FP/5P/5P), 0682001433 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 9P), 0682001434 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 9P/5P), 0682001435 (EDS LIGHT SUSPENSION, CENTRAL AXIS, FP/9P/5P) Product Usage: The Stryker Visum LED Surgical Lighting system is intended to illuminate the operative site during surgical procedures with high intensity light
Reason for recall
The potential hazard that can arise for the combination of the missing screws and the overloading by the end user is insufficient mount force that causes the equipment to fall.
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-1699-2017. 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.