Reported Aug 31, 2022 · Ongoing

HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144

Mizuho OSI

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: Mizuho OSI · 30031 Ahern Ave · Union City, CA · 94587-1234

Is this the product you have?

  • HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144
Lot codes and dates
  • Model Number6850-144
  • UDI Code(01)00842430106842(10)MIZ210712(11)210712
  • Lot/Batch NumberMIZ210712
Amount recalled
13 devices

Where it was sold

Why it was recalled

One batch of "regular" femoral hooks were incorrectly etched with the "classic" femoral hook model number.

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

Data as of Sep 19, 6:19 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.