Arthrex® AR-8935-32Recalls & reported problems
Arthrex, Inc. · LO-PRO SCRW,TI,3.5MMX 32MM · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867050587), received between Mar 9, 2020 and Mar 9, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Patient-Device Incompatibility” (1 report).
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.
Most reported problems
Device problems
- Patient-Device Incompatibility1
Patient problems
- Increased Sensitivity1
- Rash1
- Reaction1
- Visual Impairment1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 9, 2020Patient-Device Incompatibility
IT WAS REPORTED BY THE PATIENT THAT SHE HAD ANKLE RECONSTRUCTION SURGERY A FEW YEARS AGO UTILIZING ARTHREX PRODUCTS. SINCE SURGERY SHE HAS DEVELOPED REACTION TYPE SYMPTOMS WHICH INCLUDE RASHES AT THE SURGICAL SITE. PATIENT IS SEEKING MATERIAL COMPOSITION OF THE DEVICES. PATIENT WILL PROVIDE ADDITIONAL INFORMATION VIA EMAIL AND WILL OBTAIN THE SPECIFIC PART NUMBERS INVOLVED TO PROVIDE TO ARTHREX. ADDITIONAL INFORMATION OBTAINED 02/17/2020: PATIENT'S SURGERY TOOK PLACE (B)(6) 2013. PROCEDURE WAS ON HER RIGHT FOOT. SHE HAD AN ACCESSORY NAVICULAR REMOVED AND THE ARCH IN HER FOOT WAS CORRECTED. PATIENT REPORTS HER ANKLE HAS ALWAYS BEEN TENDER BUT SHE FIGURED THAT WAS NORMAL (LONG LASTING EFFECTS OF SURGERY). SHE BEGAN HAVING RASHES ON HER KNUCKLES AROUND THE END OF 2016. IN THE PAST YEAR SHE HAS HAD RASHES ON HER SHINS; WHAT LOOKS LIKE POLPHOLYX ON HER FINGERS THAT COMES AND GOES; AND A SMALL PATCH OF DRY/ CRUSTY SKIN ON HER OUTER RIGHT ANKLE. THE ONLY THING THAT SEEMS TO HELP THE PATIENT IS ORAL BENADRYL. IN (B)(6) 2018 PATIENT'S EYESIGHT SUDDENLY BECAME SENSITIZED TO HIGH CONTRACT IMAGES/ LIGHTING. PATIENT HAS HEADACHES MORE OFTEN THAN EVER BEFORE. PATIENT'S OPHTHALMOLOGIST SAYS THE S
Patient problems: Increased Sensitivity; Rash; Reaction; Visual Impairment
MAUDE report 9805059 ↗
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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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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