Product Safety Recalls

Product Recall Tracker

Arthrex, Inc. Recall 87481

Description: Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.

Arthrex, Inc. Recall 87481 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1310-2021
Event ID87481
Event DescriptionDrill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
Product TypeDevices
DistributionUS Nationwide distribution in the states of Ohio, Oregon, Tennessee, Texas.
Quantity9 units
Recall ReasonThe color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
Device Classification20210407
Device Code InfoProduct Code AR-8770-02, Lot Number 032052
Center Classification Date20210326
Recall Initiation Date20210224
Recalling FirmArthrex, Inc.
Initial Notification E-Mail
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.