Stradis Healthcare recalls vein procedure trays with incomplete bag seals that could breach sterility. Affected items have specific serial numbers and item numbers. Consumers should contact the company 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 vein procedure trays that may have incomplete bag seals, risking a breach in the sterility of the kit. This could lead to infections if the kit is used without proper sterility.
The trays may have outer bags that are incompletely sealed during manufacturing. This could allow contamination, potentially leading to infections if the kit is used without proper sterility.
Healthcare professionals using the vein procedure trays for medical procedures are most at risk. Patients receiving procedures with these kits could be affected if sterility is compromised.
Check for the item number 682-1732 on the tray. Look for the serial numbers 22230489185 or the UDI/DI codes M75268217321 (case) and M75268217320 (kit).
Identify the item number 682-1732, serial numbers 22230489185, or UDI/DI codes M75268217321 (case) and M75268217320 (kit).
The trays may have incomplete bag seals that could breach sterility, potentially leading to infections if used without proper sterility.
Check for item number 682-1732, serial number 22230489185, or UDI/DI codes M75268217321 (case) and M75268217320 (kit).
The recall record does not specify a remedy, so contact Stradis Healthcare 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-0543-2023 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0543-2023 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.
