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All product recalls associated with Arthrex, Inc..
Total Recalls
8
Past Year
0
Class I (Serious)
0
Most Recent
Nov 2022
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The devices may be packaged with the wrong reamer size.
Products do not meet length and diameter specifications.
Not properly sterilized, because the outer pouch seal on the Tyvek header was sealed closely to the foil pouch.
It was discovered that five AR-13200ST-15.0 parts were processed as AR-13200T-15.0 parts.
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
Screws provided in packaging are 5mm shorter than intended
There is a potential for blockage of the Hub Attachment Tube.
Screws provided in the device package are 6 mm longer than intended.