Stradis Healthcare recalls Kelly Curved 5.5" Forceps (Part ZZ-0701) due to potential sterile barrier compromise. Affected lots: 22027483172 and 22131487071. No remedy specified in recall notice.
The sterile barrier may be compromised.
Stradis Healthcare is recalling Kelly Curved 5.5" medical forceps (Part ZZ-0701) because the sterile barrier might be compromised. This could lead to infections during medical procedures if the forceps are used without proper sterility.
The sterile barrier is a critical component that prevents contamination during medical procedures. If compromised, it could allow pathogens to enter the surgical site, increasing infection risk for patients.
Healthcare professionals and medical facilities using the recalled forceps are most at risk. Patients using these forceps during procedures could face infection risks if the sterile barrier is compromised.
Check for the Part Number ZZ-0701 on the forceps. Affected lots are 22027483172 and 22131487071. The product is sold under Stradis Healthcare.
Identify the Part Number ZZ-0701 and lot numbers 22027483172 or 22131487071 on the forceps.
The recall notice does not specify any remedy.
Compromised sterile barriers could lead to infections during medical procedures.
Lots 22027483172 and 22131487071 are affected.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1554-2022 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-1554-2022 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.
