Recall Ledger

Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog... recall (Exactech, Inc.)

Medical deviceClass IIOngoing

Summary: Exactech, Inc. is recalling Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05. Reason: Impactor handle may be missing cross-pin.

What is being recalled

Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05

Why

Impactor handle may be missing cross-pin

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US: 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 (states named: California, Colorado, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Minnesota, Nevada, New York, Ohio, Oklahoma, Puerto Rico, South Carolina, Tennessee, Texas, Virginia, Wisconsin)

How to tell if yours is affected

Lot Code: Part Number: 321-09-05 UDI-DI: 10885862557674 Lot Number: All (Please refer to Attachment 1 - Product Information Spreadsheet for details)

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-1509-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedFebruary 3, 2026
ReportedMarch 18, 2026
CompanyExactech, Inc.
Company locationGainesville, FL, United States
Initiated byVoluntary: Firm initiated
Quantity120 units

More recalls from Exactech, Inc. · all medical device recalls · recalls from February 2026

Official FDA record