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Zimmer Orthopedic Mfg Ltd

IE Last updated 23 Oct 2026

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Devices
0
Registries
FDA
FDA recalls
1

Catalogue0

No devices listed yet from this manufacturer.

FDA recalls1

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

  • 2017

    • 24 Jul 2017 Z-0663-2018 Class II Terminated There is a possibility that the protective foam insert used during the packaging of the affected products is undersized, which may cause a breach in the inner cavity during transportation.

Information

Country
IE
Address
Building No 2 East Park, Shannon Clare
FDA FEI number
3007963827