FDA recall record

Stryker GmbH Long Nail, RIGHT Gamma4 10x320mm x 125, component of the Gamma4 System recall — FDA Z-1914-2025

Investigation confirmed that the GAMMA4 Right Long Nail was manufactured with the geometry of a left nail.

Class IIclassification
Z-1914-2025official record ID
Jun 18, 2025report date

Recall record at a glance

Official recordZ-1914-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmStryker GmbH
Report dateJun 18, 2025
Recall initiation dateMay 28, 2025
LocationSelzach, Switzerland

Official product description

Long Nail, RIGHT Gamma4 10x320mm x 125, component of the Gamma4 System. Catalog Number: 84250320S.

Why the product was recalled

Investigation confirmed that the GAMMA4 Right Long Nail was manufactured with the geometry of a left nail.

Distribution information

Worldwide - US Nationwide distribution in the states of AL, FL, NJ, OR and the countries of Australia and Japan.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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