Stradis Healthcare recalls knee packs with item 570-2908 due to potential sterility breaches from incomplete bag sealing. Affected units sold with specific serial numbers.
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
Stradis Healthcare is recalling knee surgical packs that may have incomplete bag sealing, risking sterility breaches during medical procedures. This could lead to infections if the kit is used without proper sterility.
The outer bag may not seal properly during manufacturing, creating a path for contaminants to enter the sterile kit. This breach could lead to infections during medical procedures if the kit is used without proper sterility.
Surgical teams and medical facilities using the knee pack with item number 570-2908 are most at risk. Patients undergoing surgery with this kit could face infection if sterility is compromised.
Check for the item number 570-2908 on the knee pack. Affected units have specific serial numbers: 22241489773.
Inspect the outer bag for signs of incomplete sealing, such as leaks or visible gaps.
The recall applies to specific knee packs used in medical procedures. If you have the item number 570-2908 with serial number 22241489773, contact Stradis Healthcare for guidance.
Look for the item number 570-2908 and serial number 22241489773 on the pack. Affected units were sold with these specific identifiers.
Check the sterility seal for completeness. If you find a breach, do not use the pack and contact Stradis Healthcare for instructions.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0524-2023 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0524-2023 from Stradis Healthcare. 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.
