Stradis Healthcare recalls Kelly Straight 5.5" forceps (part ZZ-0700) due to potential sterile barrier compromise. Affected lots: 22145487092 and 22154486659. No remedy specified in recall notice.
The sterile barrier may be compromised.
Stradis Healthcare is recalling Kelly Straight 5.5" medical forceps (part number ZZ-0700) 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 might not be fully intact, which could allow contamination during medical procedures. If the forceps are used without proper sterility, this could lead to infections in patients.
Medical professionals using these forceps for procedures are most at risk. Patients receiving procedures with compromised sterile barriers could face infections.
Check for the part number ZZ-0700 on the forceps. Affected lots are 22145487092 and 22154486659. These forceps were sold with the UDI/DI code M752ZZ07000.
Look for part number ZZ-0700 and affected lots 22145487092 or 22154486659 on the forceps.
The recall notice does not specify any remedy.
The recall notice does not provide specific action steps beyond checking product details.
Check for part number ZZ-0700 and affected lots 22145487092 or 22154486659 on the forceps.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1553-2022 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-1553-2022 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.
