Howmedica recalls Stryker Restoration Anatomic Hemispherical Shell Size 60 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 Restoration Anatomic Hemispherical Shell Size 60 Left. The device may fall off its post in packaging, potentially causing loose debris. This could lead to injury if the device is mishandled during shipping or storage.
The device may fall off its post within the inner packaging. This can cause loose debris that might be a hazard if the product is mishandled during shipping or storage.
Owners of the Stryker Restoration Anatomic Hemispherical Shell, Size 60 Left, Sterile, Catalog # 504-02-60D-L. Those handling the product during shipping or storage are most at risk of debris causing injury.
Check for the product name: Stryker Restoration Anatomic Hemispherical Shell, Size 60 Left, Sterile. Look for Catalog # 504-02-60D-L and UDI (01)07613327012422(17).
Identify the product by checking the Catalog # 504-02-60D-L and UDI (01)07613327012422(17) on the packaging.
The recall states the device may fall off its post in packaging, causing loose debris. However, the hazard is described as low risk, so it is not immediately dangerous to use.
The recall does not specify a remedy, so contact Howmedica directly for guidance on next steps.
Check for the product name: Stryker Restoration Anatomic Hemispherical Shell, Size 60 Left, Sterile. Look for Catalog # 504-02-60D-L and UDI (01)07613327012422(17).
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2090-2020 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2090-2020 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.
