Arthrex® AR-8770-70HRecalls & reported problems
Arthrex, Inc. · COMPR FT SCRW, 7.0 XL, 70MM LGTH · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888867263291), received between Dec 20, 2019 and Dec 20, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (2 reports).
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 Interaction Problem2
- Patient-Device Incompatibility2
Patient problems
- Fever2
- Reaction2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 20, 2019Patient-Device Incompatibility; Patient Device Interaction Problem; Patient-Device Incompatibility; Patient Device Interaction Problem
IT WAS REPORTED AFTER FOOT RECONSTRUCTION PROCEDURE ARTHROCELL WAS USED. THE PATIENT HAD AN ADVERSE REACTION INCLUDING FEVER SPIKES ONE DAY POST-OP. THERE WERE ALSO FOUR SCREWS AND TWO STAPLES IMPLANTED. NO REVISION IS PLANNED AT THIS TIME. CURRENTLY THE DOCTOR IS RESEARCHING THE SOURCE OF THE REACTION.
Patient problems: Fever; Reaction
MAUDE report 9506220 ↗InjuryDec 20, 2019Patient-Device Incompatibility; Patient Device Interaction Problem; Patient-Device Incompatibility; Patient Device Interaction Problem
IT WAS REPORTED AFTER FOOT RECONSTRUCTION PROCEDURE ARTHROCELL WAS USED. THE PATIENT HAD AN ADVERSE REACTION INCLUDING FEVER SPIKES ONE DAY POST-OP. THERE WERE ALSO FOUR SCREWS AND TWO STAPLES IMPLANTED. NO REVISION IS PLANNED AT THIS TIME. CURRENTLY THE DOCTOR IS RESEARCHING THE SOURCE OF THE REACTION.
Patient problems: Fever; Reaction
MAUDE report 9506199 ↗
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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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