Howmedica recalls Stryker Orthopaedics Restoration Anatomic Hemispherical Shell Size 54 Left. Packaging may fall off causing loose device with debris. Consumers should check product details and contact Howmedica for remedy.
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 Stryker Orthopaedics' Restoration Anatomic Hemis: Size 54 Left, Sterile, Catalog # 504-02-54C-L. The device may fall off its post in the inner packaging, potentially leaving debris loose. This could cause injury if the device is mishandled during use.
The device may fall off its post within the inner packaging, which can cause the device to become loose with coating debris. This poses a risk if the loose device is handled improperly during surgery or if debris is accidentally introduced into the surgical site.
Patients who received the Stryker Orthopaedics Restoration Anatomic Hemispherical Shell (RAS) Size 54 Left, Sterile, Catalog # 504-02-54C-L for surgery. Surgeons and medical staff using the device during procedures are most at risk.
Check for the product name 'Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell', size 54 left, sterile, catalog number 504-02-54C-L, and the UDI (01)07613327012354(17). The device was sold with specific lot numbers listed in the recall notice.
Verify the product name, size, and catalog number to confirm if it is recalled.
Reach out to Howmedica for further instructions on the remedy.
The recall states the device may fall off its post in the packaging, but it does not indicate that the device is dangerous when used correctly.
Check the product details and contact Howmedica for specific instructions on the remedy.
Look for the product name 'Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell', size 54 left, sterile, catalog number 504-02-54C-L, and the UDI (01)07613327012354(17).
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2084-2020 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2084-2020 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.
