Stryker recalls Berchtold Chromophare Dual Monitor Carrier Arms with serial numbers DFP-075-0307-0001 to DFP-075-1014-0230 due to potential insufficient welds in mounts.
The mounts on the monitor may have an insufficient weld.
Stryker is recalling Berchtold Chromophare Dual Monitor Carrier Arms that may have insufficient welds in the mounts. This could lead to the monitor falling off the ceiling mount, posing a risk of injury.
The mounts on the monitor may have an insufficient weld, which could cause the monitor to detach from the ceiling mount. If the monitor falls, it might hit people or equipment, causing injury.
Surgical staff and facilities using the Berchtold Chromophare Ceiling Mounted Surgical Light System with the recalled carrier arms are affected. Those who have the specific serial numbers listed are most at risk.
Check if your Berchtold Chromophare Dual Monitor Carrier Arm has a serial number between DFP-075-0307-0001 and DFP-075-1014-0230. This is part of the Berchtold Chromophare Ceiling Mounted Surgical Light System.
Verify your carrier arm's serial number to see if it falls within the range DFP-075-0307-0001 to DFP-075-1014-0230.
Reach out to Stryker Communications for further assistance or to confirm if your item is affected.
The recalled item is the Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, part of the Berchtold Chromophare Ceiling Mounted Surgical Light System.
Check the serial number on your carrier arm; if it is between DFP-075-0307-0001 and DFP-075-1014-0230, it is affected.
Contact Stryker Communications to confirm if your item is affected and for further instructions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2446-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2446-2019 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
