AVID Medical recalls medical convenience kits for laparoscopic prostatectomy due to discoloration from resterilization. Affected kits may have visual issues during surgery.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling medical convenience kits used in laparoscopic prostatectomy procedures because the visualization system was resterilized incorrectly, causing discoloration. This could affect the clarity of the surgical view during procedures.
The Clearify Visualization System in the kits was resterilized incorrectly, leading to discoloration. This could reduce the clarity of the surgical view during procedures, potentially affecting the precision of the surgery.
Medical professionals using the specific laparoscopic prostatectomy kits with model number NIHB0036-07 and lot numbers 1589877 or 1612565 are affected. Patients undergoing surgery with these kits may be at risk of visual issues.
Check for the model number NIHB0036-07 and lot numbers 1589877 or 1612565 on the kit packaging. The kits are used in laparoscopic prostatectomy procedures.
Verify the model number (NIHB0036-07) and lot numbers (1589877 or 1612565) on the kit packaging.
The recall is for discoloration in the visualization system, which may affect surgical clarity but does not pose a risk of serious injury or death.
Check the model number and lot numbers on the kit packaging. If you have the affected model and lot numbers, contact AVID Medical for further instructions.
Look for the model number NIHB0036-07 and lot numbers 1589877 or 1612565 on the kit packaging.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2255-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2255-2025 from AVID Medical. 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.