Reported Apr 6, 2022 · Terminated

EasyFuse Dynamic Compression System Instrument Pack

Wright Medical Technology, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Wright Medical Technology, Inc. · 1023 Cherry Rd · Memphis, TN · 38117-5423

Is this the product you have?

  • EasyFuse Dynamic Compression System Instrument Pack
Lot codes and dates
  • Model Number FFSP1530
  • UDI00889797103565
  • Lot Codes (Expiration Date)781853-110321 (11/03/2029) and 780395-112221 (12/03/2029)
Amount recalled
176 packs

Where it was sold

Why it was recalled

The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 1, 2026 · Data as of Sep 19, 6:17 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.