Stradis Healthcare recalls Lipo procedure trays with potential sterility breaches due to incomplete sealing. Affected items have specific serial numbers and item numbers. Consumers should check their products and contact Stradis Healthcare for details.
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 certain surgical trays that may have incomplete sealing, risking sterility breaches. This could lead to infections if used without proper sterilization.
The trays may have outer bags that aren't sealed properly, which can cause sterility breaches. This means the surgical kits might not be sterile when used, increasing infection risks.
Healthcare professionals and surgical staff who use the recalled trays. Those handling medical procedures with these trays are most at risk.
Check for item number 681-254, serial numbers starting with 22270492010, or UDI/DI codes M7526812541 (case) and M7526812540 (kit).
Look for item number 681-254, serial numbers starting with 22270492010, or UDI/DI codes M7526812541 (case) and M7526812540 (kit).
The outer bags may not be sealed properly, which can cause sterility breaches and increase infection risks.
Check for item number 681-254, serial numbers starting with 22270492010, or UDI/DI codes M7526812541 (case) and M7526812540 (kit).
The recall does not specify a remedy, so contact Stradis Healthcare directly for further 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-0536-2023 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0536-2023 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.
