Augmedics recalls Perc Pin Adaptor model AMCH07200 due to improper tightening markings. This component of the xvision Spine system may be inconvenient for users. Affected units include specific lot numbers.
The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient to the user and the tightening markings found to be improperly placed.
Augmedics is recalling a specific Perc Pin Adaptor component (model AMCH07200) used in spinal surgery systems because its tightening markings are placed incorrectly. This could make it harder for surgeons to use the device properly during procedures.
The tightening markings on the Perc Pin Adaptor's knob are improperly placed, making it inconvenient for users. This could lead to difficulty in adjusting the device during spinal surgery procedures.
Surgeons using the xvision Spine (XVS) system for spinal surgery may own this component. The risk is low as the issue is about usability, not safety.
Check for the model number AMCH07200 on the Perc Pin Adaptor. The product is part of the xvision Spine (XVS) system used in spinal surgery. Lot numbers range from 038110 to 054926.
Identify the model number AMCH07200 on the Perc Pin Adaptor to confirm it is affected.
No, the hazard is about usability, not safety. The issue is that the tightening markings are improperly placed, which could make the device inconvenient but not cause injury.
The recall does not specify a remedy, so no action is required. Check the model number and lot numbers to confirm if it is affected.
Look for the model number AMCH07200 on the Perc Pin Adaptor. The product is part of the xvision Spine (XVS) system used in spinal surgery, and lot numbers range from 038110 to 054926.
We’ve drafted a message you can send Augmedics to request your refund or repair — edit it as you like.
Subject: Recall Z-1761-2025 — Augmedics Augmedics Hello, I own a Augmedics that is covered by recall Z-1761-2025 from Augmedics. 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.
