FDA Device recall Z-1602-2020
Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000
- FDA Device
- Class II
- terminated
- Published 2020-04-08
On 2020-04-08 the FDA classified a Class II recall of Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000 by Stryker Communications, citing the firm has become aware that there is a likelihood that a missing snap ring or spanner nut may result in an insufficient mount force that causes the surgical light to fall. If t….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1602-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-10-11 |
| Published | 2020-04-08 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Stryker Communications |
| Distribution | US |
Product
Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000
Reason
The firm has become aware that there is a likelihood that a missing snap ring or spanner nut may result in an insufficient mount force that causes the surgical light to fall. If the suspension of the surgical light falls, it may potentially cause serious injuries to Health Care Providers and/or patients.
Identifiers
| code_info | Serial Number Range: 091316 70016 through 083117-73252 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1602-2020%22
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