Class II U.S. Food and Drug Administration

Exactech, Inc. Brand Name: Equinoxe Ergo Product Name: Adjustable Angle rTSA Reamer recall: Due to products that have not completed design updates and performance

Recall published 11 months ago

Due to products that have not completed design updates and performance testing being released/distributed. Products may not conform to design and performance criteria.

The hazard: Device safety concern

The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

What the notice says: Due to products that have not completed design updates and performance testing being released/distributed. Products may not conform to design and performance criteria.

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-0535-2026
Published
November 26, 2025
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Exactech, Inc.
Product type
Medical devices
Units affected
1
Distribution
South Carolina
Made in
United States
Lot / code info
Lot Code: Part Number: 321-59-42, UDI-DI: 10885862593009, Lot Number: 410398-013
UPC codes
10885862593009

Products covered by this recall

Brand Name: Equinoxe Ergo Product Name: Adjustable Angle rTSA Reamer, 42mm Model/Catalog Number: 321-59-42 Software Version: N/A Product Description: rTSA Reamer, 42mm Component: Not a component

Check your product

The notice names 5 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 10885862593009

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 410398-013 — 1

Model or item number

On the rating label, the box or the instruction sheet.

  • 321-59-42 Software Version
  • 321-59-42
  • UDI-DI

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

Exactech, Inc. — The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.
  3. Ask the supplier or clinic that provided it what the remedy is in your case.
  4. If you are a facility, quarantine affected stock and log the correction.

Who pays for a device recall

The manufacturer funds the remedy. The practical question is usually which link in the chain executes it.

  • If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.
  • Ask for written confirmation that the remedy was applied to your serial number. That is what an insurer or a future clinician will want to see.
  • If you bought it yourself online or from a pharmacy, go to the manufacturer’s recall page rather than the retailer; device claims are handled centrally.
  • Where the remedy is a software update, there is nothing to claim, but do confirm the version changed afterwards.

Company contact: Exactech, Inc. — 2320 Nw 66th Ct, Gainesville, FL, 32653-1630

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Exactech, Inc. medical devices recalled?

Due to products that have not completed design updates and performance testing being released/distributed. Products may not conform to design and performance criteria. Due to products that have not completed design updates and performance testing being released/distributed. Products may not conform to design and performance criteria.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 10885862593009; lot code 410398-013 — 1; model number 321-59-42 Software Version, 321-59-42, UDI-DI. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.

Which states were affected?

The notice lists South Carolina.

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