Perc Pin Adaptor AMCH07200Recalls & reported problems
Augmedics Ltd · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Apr 14, 2025Open, Classified
The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient to the user and the tightening markings found to be improperly placed.
Z-1761-2025 · Root cause: Device Design · Recall details · FDA record ↗
Other Orthopedic Augmented Reality devices
- ARVIS ® IN-28000Kico Knee Innovation Company Pty Limited · Orthopedic Augmented Reality2 recalls0 reports
- All-in-one computer + Pre-installed Software ACC00008Augmedics Ltd · Orthopedic Augmented Reality26 reports
- XVS Headset IPD-60 Clear Display AHMD601WLTAugmedics Ltd · Orthopedic Augmented Reality4 reports
- XVS Straight Clamp AMCH00005Augmedics Ltd · Orthopedic Augmented Reality3 reports
- NextAR Spine Platform 03.57.10.0026Medacta International SA · Orthopedic Augmented Reality2 reports
- NextAR Spine Platform 03.57.10.0173Medacta International SA · Orthopedic Augmented Reality2 reports
- MyKnee NextAR Tibial Distal Cutting Block Efficiency 15.1242Medacta International SA · Orthopedic Augmented Reality1 report
- NextAR TKA Platform 02.23.10.0011Medacta International SA · Orthopedic Augmented Reality1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page