Stradis Healthcare recalls basin sets with item #570-1803 due to potential sterility breaches from incomplete bag sealing. Affected units include specific UDI/DI and serial numbers. Consumers should check their product 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 basin sets with item number 570-1803 because the outer bags may not seal properly, risking contamination during medical procedures. This could lead to infections if the kits are used without proper sterility.
The outer bag may not seal completely during manufacturing, which could allow contamination of the sterile medical kit. If the kit is used without proper sterility, it might lead to infections during medical procedures.
Healthcare professionals and medical facilities using the basin set with item number 570-1803 are most at risk. Patients using these kits during surgery or procedures could face infection if sterility is compromised.
Check for the item number 570-1803 on the basin set. Look for UDI/DI (case) H65857018031 or UDI/DI (kit) M75257018030, and serial numbers starting with 22258490734.
Identify the item number, UDI/DI codes, and serial numbers to confirm if your basin set is affected.
The recall is for potential sterility breaches, which could lead to infections if the kit is used without proper sterility. However, the risk is low as the issue is related to manufacturing conditions, not immediate harm.
Check for the item number 570-1803, UDI/DI (case) H65857018031, UDI/DI (kit) M75257018030, and serial numbers starting with 22258490734.
The recall record does not specify a remedy, so affected users should check with 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-0508-2023 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0508-2023 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.
