Class II — Stryker Communications
| Recalling firm | STRYKER CORP. |
|---|---|
| Registered facility | View this company's 61 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential incomplete final weld on the drop tube flange. |
| Product | Stryker Visum 300 Ceiling-mounted Exam Light. |
| Quantity | 1,375 units |
| Distribution | Worldwide Distribution: US natiowide and to the country of Canada. |
| Initiated | 2013-07-25 |
| Classified | 2013-08-21 |
| Terminated | 2015-04-03 |
| Recall number | Z-1992-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Stryker Communications (Z-1992-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65888/
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