Stryker Visum 300 Ceiling-mounted Exam Light — Class II medical device recall Z-1992-2013
Terminated recall by Stryker Communications, reported 2013-08-28. Potential incomplete final weld on the drop tube flange.
| Recall number | Z-1992-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Communications, Flower Mound, TX, United States |
| Recall initiated | 2013-07-25 |
| Classified | 2013-08-21 |
| Reported by FDA | 2013-08-28 |
| Terminated | 2015-04-03 |
| Countries outside the US | CA |
| Quantity | 1,375 units |
| Model numbers | 0682001410A, 0682001410B, 0682001410C, 0682001410D, 0682001410E, 0682001410F, 0682001410G, 0682001410H |
Product
Stryker Visum 300 Ceiling-mounted Exam Light.
Reason for recall
Potential incomplete final weld on the drop tube flange.
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-1992-2013. 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.