Stryker Mako recalls specific lots of Vizadisc Hip and Knee Procedure Tracking Kits due to potential reflective material damage causing camera detection failure. Affected units include catalog numbers 107130 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 Vizadisc Hip and Knee Procedure Tracking Kits because the reflective material might get damaged, making the kit undetectable by cameras during surgery. This could lead to tracking errors during surgical procedures.
The reflective material in the tracking kits can become damaged, which prevents the camera from detecting the kit properly. This might cause tracking errors during surgery, potentially affecting the precision of the procedure.
Surgical teams using the specific lots of Vizadisc Hip and Knee Procedure Tracking Kits for orthopedic surgeries. The risk is highest for medical professionals handling these kits during procedures.
Check the catalog number (107130) and lot numbers listed: 17007K, 17013K, 17024K, 17035K, 17054K, 16354H, 17097K, 17124K, 17129K, 17136K, 17143K, 17103H.
Review the lot numbers on your Vizadisc Hip or Knee Procedure Tracking Kit to see if they match the affected list: 17007K, 17013K, 17024K, 17035K, 17054K, 16354H, 17097K, 17124K, 17129K, 17136K, 17143K, 17103H.
The catalog number is 107130.
Affected lot numbers include 17007K, 17013K, 17024K, 17035K, 17054K, 16354H, 17097K, 17124K, 17129K, 17136K, 17143K, 17103H.
The damaged reflective material can cause the tracking kit to be undetectable by the camera, potentially leading to tracking errors during surgical procedures.
We’ve drafted a message you can send Stryker Mako to request your refund or repair — edit it as you like.
Subject: Recall Z-2925-2018 — Stryker Mako Stryker Mako Hello, I own a Stryker Mako that is covered by recall Z-2925-2018 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.
