Stradis Healthcare recalls NARMD MEDICAL DEPOT Iris Curved Scissors (Part ZZ-0697) due to potential compromised sterile barrier. Affected units include specific lots and serial numbers.
The sterile barrier may be compromised.
Stradis Healthcare is recalling a specific model of medical scissors because the sterile barrier might be damaged. This could lead to infections or contamination during medical procedures. Affected users should check their product details and follow the official recall steps.
The sterile barrier is a critical protective layer that keeps medical tools clean and infection-free. If this barrier is compromised, it could allow bacteria to enter the scissors, increasing infection risk during procedures.
Healthcare professionals and medical facilities using the NARMD MEDICAL DEPOT Iris Curved Scissors (Part ZZ-0697) are most at risk. Patients using these scissors during procedures could face infection risks if the sterile barrier is compromised.
Check for the part number ZZ-0697 on the scissors. Affected units include specific lots: 22026482044 and 22152487922, and serial numbers starting with M752ZZ06970.
Look for the part number ZZ-0697 and specific lots (22026482044 or 22152487922) on the scissors.
The sterile barrier may be compromised, which could lead to infection risks during medical procedures.
Check the product details for the part number and lots to see if your scissors are affected. If they are, contact Stradis Healthcare for further instructions.
Yes, a compromised sterile barrier could allow bacteria to enter the scissors, increasing infection risk during medical procedures.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1552-2022 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-1552-2022 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.
