FDA Device recall Z-2446-2019
Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light Syst…
- FDA Device
- Class II
- terminated
- Published 2019-09-11
On 2019-09-11 the FDA classified a Class II recall of Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light Syst… by Stryker Communications, citing the mounts on the monitor may have an insufficient weld.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2446-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-08-01 |
| Published | 2019-09-11 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Stryker Communications |
| Distribution | CA, CO, CT, FL, GA, IL, IN, MD, MI, MN, MO, NC, NH, NJ, NY, OH, PA, SC, TN, TX, WI |
Product
Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light System.
Reason
The mounts on the monitor may have an insufficient weld.
Identifiers
| code_info | Serial numbers DFP-075-0307-0001 to DFP-075-1014-0230. |
|---|
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-2446-2019%22
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