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Open, Classified

Brand Name: Equinoxe Ergo Product Name: Ergo Augments Pilot Tip Converter Model/Catalog Number: 301-11-11 Software Version: N/A Product Description: Pilot Tip Converter Piece Component: Not a component

FDA Recall Z-0537-2026 · Posted 2025-11-17

Recalling FirmExactech, Inc.
Recall StatusOpen, Classified
Product CodePHX
Date Initiated2025-09-05
Product Quantity1

Reason for Recall

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

Firm Action

On 09/05/2025, the firm emailed an "URGENT MEDICAL DEVICE RECALL NOTICE" to customers informing that, during routine inventory review, it was discovered that the a number of parts/products, which were pending design verification testing were incorrectly placed in active internal inventory rather than designated quarantine locations. Several part/products were distributed to customers. Customers are instructed to: "Carefully review this notification to ensure that they fully understand the issue and all actions required. "Immediately identify, quarantine, and return any of the subject devices in their inventory and/or customer s inventory. "Stop and cease use of any affected devices. "Notify all their accounts that may have received these products and extend this recall notice, including the Description of Issue and Potential Clinical Impact, to them. "Complete and Return the attached Recall Inventory Response Form to Exactech via email at [email protected]. For questions or assistance - contact Recall Support Team at [email protected]

Root Cause

Release of Material/Component prior to receiving test results

Distribution Pattern

U.S.: SC O.U.S.: N/A

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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