Howmedica recalls Stryker Restoration Anatomic Hemispherical Shell Size 64 right. Packaging may fall off, causing loose device with debris. Stop using if found.
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 Restoration Anatomic Hemispherical Shell Size 64 right. The device may fall off its post in the inner packaging, potentially causing debris to become loose. This could lead to injury if the device is mishandled during use.
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, which could potentially lead to injury if mishandled during use.
Patients who received this specific surgical implant from Howmedica Osteonics Corp. are most at risk if the packaging falls off during handling.
Check for the product name: Stryker Restoration Anatomic Hemispherical Shell, Size 64 right. Look for the catalog number 504-02-64E-R and the UDI (01)07613327012460(17).
Inspect the inner packaging for the device falling off its post with coating debris.
The recall is for packaging issues, not the product itself. The device is safe to use once properly installed.
Look for the catalog number 504-02-64E-R and UDI (01)07613327012460(17) on the packaging.
Check the inner packaging for the device falling off its post with coating debris. If found, stop using it and contact Howmedica.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2096-2020 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2096-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.