Stryker Mako recalls specific lots of Vizadisc Knee Procedure Tracking Kit due to reflective material damage causing camera detection issues. Affected units include catalog numbers 107120 with listed lot numbers.
Specific lots of the Vizadisc Knee Procedure Tracking Kit and Vizadisc Hip Procedure Tracking Kit have the potential to be damaged on the Vizadisc reflective material causing an inability to be detected by the camera.
Stryker Mako is recalling specific lots of the Vizadisc Knee Procedure Tracking Kit because the reflective material may become damaged, preventing camera detection. This could lead to tracking issues during surgical procedures. The recall affects only specific lot numbers and catalog numbers.
The reflective material in the Vizadisc kit can become damaged, causing the camera to fail in detecting the tracking system. This may lead to tracking issues during surgical procedures but does not pose a direct physical hazard to patients or users.
Surgical teams using the Vizadisc Knee Procedure Tracking Kit with specific lot numbers (17007K, 17013K, etc.) are affected. The risk is low as the issue is limited to the reflective material not being detected by cameras during surgery.
Check the catalog number (107120) and lot numbers listed: 17007K, 17013K, 17024K, 17035K, 17054K, 16354H, 17097K, 17124K, 17129K, 17136K, 17143K, 17103H.
Verify the catalog number (107120) and lot numbers listed in the recall notice.
The reflective material in specific lots may become damaged, causing the camera to fail in detecting the tracking system.
Lot numbers 17007K, 17013K, 17024K, 17035K, 17054K, 16354H, 17097K, 17124K, 17129K, 17136K, 17143K, 17103H.
The recall does not require immediate action; check the lot numbers to see if your kit is affected.
We’ve drafted a message you can send Stryker Mako to request your refund or repair — edit it as you like.
Subject: Recall Z-2924-2018 — Stryker Mako Stryker Mako Hello, I own a Stryker Mako that is covered by recall Z-2924-2018 from Stryker Mako. 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.
