Stradis Healthcare recalls Anterior Hip Pack surgical kits with potential sterility breaches due to outer bag perforations. Affected kits include specific SKUs and lot numbers. Consumers should contact for remedy.
The outer bag may be perforated or torn, which may result in a breach in the sterility of the kit.
Stradis Healthcare is recalling Anterior Hip Pack surgical kits because the outer bag might tear or get punctured, risking contamination of the sterile instruments. This could lead to infections during surgery if the kit is used without proper sterility.
The outer bag can tear or puncture, which breaks the sterile seal of the surgical kit. If the bag is compromised, the instruments inside may become contaminated, increasing infection risk during surgery.
Surgical teams and hospitals using the recalled Anterior Hip Pack surgical kits. Patients undergoing hip surgery are at risk if the kit is used without the outer bag being intact.
Check the SKU/Part Number 570-2677 on the kit. Look for lot numbers: 20170461910, 20163461674, 20170462303, 20219463245, 20238464203, 20268464581, 21082472172, 21110472562, 21138473542, 21167474498, 21287478853, 21349479943.
Verify the SKU/Part Number 570-2677 and lot numbers listed in the recall notice.
The outer bag may tear or puncture, risking contamination of the sterile instruments and increasing infection risk during surgery.
Check for SKU/Part Number 570-2677 and lot numbers: 20170461910, 20163461674, 20170462303, 20219463245, 20238464203, 20268464581, 21082472172, 21110472562, 21138473542, 21167474498, 21287478853, 21349479943.
The recall notice does not specify a remedy, so contact Stradis Healthcare directly 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-0865-2022 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0865-2022 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.
