Stradis Healthcare recalls Lum Lam Custom Pack Anesthesia Kits with potential sterility breaches due to perforated outer bags. Affected units include specific lot numbers and SKUs. Consumers should check their kit's details to determine if recalled.
The outer bag may be perforated or torn, which may result in a breach in the sterility of the kit.
Stradis Healthcare is recalling Lum Lam Custom Pack Anesthesia Kits because the outer bag might tear or puncture, risking contamination of the sterile kit. This could lead to infections if the kit is used without proper sterility.
The outer bag of the anesthesia kit can tear or puncture, which may compromise the sterility of the kit. If the kit is used without proper sterility, it could lead to infections or other complications.
Healthcare professionals using the Lum Lam Custom Pack Anesthesia Kit are likely affected. The risk is highest for those who have the specific lot numbers mentioned in the recall.
Check the product's SKU/Part Number 570-2674 and UDI H65257026741. Affected units have lot numbers 21300478831 or 21314479685.
Verify your kit's SKU/Part Number 570-2674 and UDI H65257026741 to confirm if it's affected.
The recall is for potential sterility breaches due to torn or perforated bags, which could lead to infections if the kit is used without proper sterility. However, the risk is low if the kit is not used.
Check your kit's SKU/Part Number and UDI to see if it's in the affected lot numbers. If it is, contact Stradis Healthcare for further instructions.
Look for SKU/Part Number 570-2674 and UDI H65257026741 with lot numbers 21300478831 or 21314479685.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0863-2022 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0863-2022 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.
