Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel — Class II medical device recall Z-2446-2019
Terminated recall by Stryker Communications, reported 2019-09-11, distributed in CA, CO, CT, FL, GA, IL, IN, MD…. The mounts on the monitor may have an insufficient weld.
| Recall number | Z-2446-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Communications, Flower Mound, TX, United States |
| Recall initiated | 2019-08-01 |
| Classified | 2019-08-30 |
| Reported by FDA | 2019-09-11 |
| Terminated | 2021-04-27 |
| Distributed | CA, CO, CT, FL, GA, IL, IN, MD, MI, MN, MO, NC, NH, NJ, NY, OH, PA, SC, TN, TX, WI |
| Countries outside the US | CA, DE |
| Quantity | 52 devices |
| Serial numbers | DFP-075-0307-0001, DFP-075-1014-0230 |
Product
Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light System.
Reason for recall
The mounts on the monitor may have an insufficient weld.
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-2446-2019. 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.