Arthrex, Inc.
6875 Arthrex Commerce Drive, Ave Maria, FL, US
Registered product codes
104 product codes
Recent MDR events
34,221 on file
- SUTR ANCH,BIO-COMP S-TAKJul 31, 2026Malfunction1220246-2026-04133
- BIO-COMP SWVLK C, CLD 4.75X19.1MMJul 31, 2026Malfunction1220246-2026-04134
- BIO-COMP SWVLK C, CLD 4.75X19.1MMJul 31, 2026Malfunction1220246-2026-04135
- SUTR ANCH,BIO-COMP S-TAKJul 31, 2026Malfunction1220246-2026-04136
- BIO-COMPSI CRKSCRW FT 4.5X 14MMJul 31, 2026Malfunction1220246-2026-04137
- SUTURELASSO, 25 DEGREE TIGHT CURVE RIGHTJul 31, 2026Malfunction1220246-2026-04138
- SUTR ANCH,BIO-COMP S-TAKJul 31, 2026Malfunction1220246-2026-04139
- SUTR ANCH,BIO-COMP S-TAKJul 31, 2026Malfunction1220246-2026-04140
- Low-Profile AC Implant DeviceJul 31, 2026Malfunction1220246-2026-04141
- KL 1.8 FiberTak, ShoulderJul 31, 2026Malfunction1220246-2026-04142
Recalls
28 on file
- Open, ClassifiedDec 8, 2022
The devices may be packaged with the wrong reamer size.
View FDA record ↗ - TerminatedUnknown
Arthrex part number AR-501-UFLC, size 3, batch 10123297, has the incorrect part number AR-501 UFRA, size 1 printed on the patient label inside the box.
View FDA record ↗ - Open, ClassifiedUnknown
The Li-ion Battery Housing for the AR-400 DrillSaw Sports 400 System may not provide a complete seal around the battery, allowing for potential fluid ingress.
View FDA record ↗ - Open, ClassifiedUnknown
There is potential to break during use.
View FDA record ↗ - Open, ClassifiedUnknown
Potentially lead to anchor breakage during insertion,
View FDA record ↗ - TerminatedUnknown
There is a potential for blockage of the Hub Attachment Tube.
View FDA record ↗ - TerminatedUnknown
Products do not meet length and diameter specifications.
View FDA record ↗ - TerminatedUnknown
Devices reported to have a smooth texture to the outer surface of the metal, which differed from a previous that had a textured outer surface.
View FDA record ↗ - TerminatedUnknown
Devices may generate excessive heat during use.
View FDA record ↗ - TerminatedUnknown
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
View FDA record ↗
Compliance history
Matched by FEI 3010331645.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.