FDA Device recall Z-1992-2013
Stryker Visum 300 Ceiling-mounted Exam Light
- FDA Device
- Class II
- terminated
- Published 2013-08-28
On 2013-08-28 the FDA classified a Class II recall of Stryker Visum 300 Ceiling-mounted Exam Light by Stryker Communications, citing potential incomplete final weld on the drop tube flange.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1992-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-07-25 |
| Published | 2013-08-28 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Communications |
| Distribution | n/a |
Product
Stryker Visum 300 Ceiling-mounted Exam Light.
Reason
Potential incomplete final weld on the drop tube flange.
Identifiers
| code_info | Product sold under the following part numbers: 0682001410A, 0682001410B, 0682001410C, 0682001410D, 0682001410E, 068200…Product sold under the following part numbers: 0682001410A, 0682001410B, 0682001410C, 0682001410D, 0682001410E, 0682001410F, 0682001410G, and 0682001410H and shipped prior to February 28, 2013. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1992-2013%22
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