Howmedica recalls Stryker Orthopaedics Restoration Anatomic Hemispherical Shell Size 62 right. Loose device in packaging may cause coating debris. Check catalog # 504-02-62E-R for affected units.
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 Hemispherical Shell (Size 62 right) due to a risk of the device falling off its post in the inner packaging. This could lead to loose device with coating debris. The recall affects specific sterile surgical implants sold with certain catalog numbers.
The device may fall off its post within the inner packaging, potentially becoming loose with coating debris. This could cause the device to be improperly positioned during surgical procedures if the packaging is opened or handled incorrectly.
Surgical professionals using the Stryker Orthopaedics Restoration Anatomic Hemispherical Shell (Size 62 right) for procedures. Most at risk are those handling the specific sterile implants with the listed catalog numbers.
Check for the catalog number 504-02-62E-R on the packaging. Affected units were sold with specific lot numbers listed in the recall notice. The product is a sterile surgical implant for orthopedic procedures.
Look for the catalog number 504-02-62E-R on the packaging to confirm if the device is affected.
The recall is for packaging risks, not the device itself. If the packaging is intact, the device is safe to use as long as it's handled properly.
Check for the catalog number 504-02-62E-R on the packaging. Affected units have specific lot numbers listed in the recall notice.
The recall does not require immediate action. Check the packaging for the catalog number to confirm if it's affected. If affected, contact Howmedica for further instructions.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2093-2020 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2093-2020 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.
