Howmedica recalls Stryker Orthopaedics Restoration Anatomic Hemispherical Shell Size 64 left. The device may fall off its post in packaging, causing loose debris. Consumers should check product details and contact Howmedica for guidance.
The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris.
Howmedica is recalling Stry: Stryker Orthopaedics Restoration Anatomic Hemispherical Shell, Size 64 left, Sterile, Catalog # 504-02-64E-L. The device may fall off its post in packaging, potentially causing loose debris. This recall is for safety reasons to prevent potential damage to the device.
The Stryker Restoration Anatomic Shell may fall off its post within the inner packaging. This can cause the device to become loose with coating debris, potentially leading to damage or injury during handling.
Patients or healthcare providers who own or use the specific Stryker Orthopaedics Restoration Anatomic Hemispherical Shell, Size 64 left, Sterile, Catalog # 504-02-64E-L. Those most at risk are individuals handling the device during packaging or shipping.
Check for the product name: Stryker Orthopaedics Restoration Anatomic Hemispherical Shell, Size 64 left, Sterile. Look for the catalog number 504-02-64E-L and the UDI (01)07613327012484(17) on the packaging.
Verify the product name, catalog number, and UDI on the packaging to confirm if it is recalled.
The recall is for packaging issues, not use. The device is safe when used properly but may have packaging problems.
The recall record does not specify a remedy or replacement process.
The recall record does not specify a remedy or replacement process.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2094-2020 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2094-2020 from Howmedica. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
