Howmedica recalls Stryker Orthopaedics Restoration Anatomic Hemispherical Shell Size 58 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 Stryker Orthopaedics' Restoration Anatomic Hemispherical Shell (Size 58 Left) because it may fall off its post in the inner packaging, potentially leaving debris loose. This could cause issues during handling or use, but the recall focuses on packaging safety rather than direct user injury.
The device may detach from its post inside the packaging, leading to loose debris. This could cause the device to become unstable or create a hazard during handling, but it does not involve direct user injury in normal use.
Patients or healthcare providers who own or use the specific Stryker Orthopaedics Restoration Anatomic Hemispherical Shell (Size 58 Left) with the listed catalog number and lot numbers. Those handling the device in packaging are most at risk.
Check for the product name 'Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell', size 58 left, sterile, catalog number 504-02-58D-L, and the listed lot numbers. The UDI (unique device identifier) is also provided in the recall.
Verify the product name, size, catalog number, and lot numbers to confirm if your item is affected.
The recall addresses potential loose debris in packaging, not direct user injury. The device is safe for use once properly installed.
Check for the specific catalog number 504-02-58D-L and the listed lot numbers in the recall notice.
The recall does not specify a remedy, so contact Howmedica directly for guidance.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2087-2020 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2087-2020 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.
