Home/Recalls/FDA-Z-1510-2026
FDA DevicesClass II

Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog...

Published: March 18, 2026Recall ID: Z-1510-2026Category: devicesCountry: US

Reason for Recall / Hazard

Impactor handle may be missing cross-pin

Product Description & Identification

Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311X

Affected Products

Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311X

Additional Source Details

FieldValue
CityGainesville
StateFL
Event id98376
Address 12320 Nw 66th Ct
Address 2N/A
Code infoAll Lots/ UDI-DI: 10885862559166
Postal code32653-1630
Report date20260318
Product typeDevices
Product quantity596 kits
Reason for recallImpactor handle may be missing cross-pin
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260203
Initial firm notificationLetter
Center classification date20260309

Overview

  • Recalling FirmExactech, Inc.
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS: CA CO FL GA HI ID IL IN KS KY LA MA MD ME MN NV NY OH OK PR SC TN TX VA WI OUS: Australia France Germany Italy Japan Korea Spain Switzerland United Kingdom United Arab Emirates Slovenia
Official Agency Alert