Trokamed recalls a specific gastroenterology-urology endoscopic access overtube (REF: WA2PS20S) due to potential kidney damage from rapid blood flow buildup. Affected units have lot numbers starting with 154125.
If the inflow speed is too quick, it could result in reduced outflow through the shaft due to blood, tissue fragments and kidney stone fragments, and quickly build up of intrarenal pressure.
Trokamed is recalling a specific type of endoscopic access tube used in medical procedures because it could cause kidney damage if blood and tissue fragments build up too quickly. This risk occurs when the inflow speed is too fast, potentially leading to dangerous pressure buildup in the kidneys.
If blood, tissue fragments, or kidney stones flow too quickly through the tube, the system may not properly remove them. This can cause a rapid buildup of pressure inside the kidney, potentially leading to kidney damage.
Medical professionals using this specific endoscopic access tube for procedures involving the gastrointestinal or urinary tract are most at risk. Patients undergoing these procedures with the recalled model may also be affected.
Check for the model number WA2PS20S on the tube. Affected units have lot numbers starting with 154:125. This product was sold with the reference number WA2PS20S.
Look for the model number WA2PS20S and lot numbers starting with 154125 on the tube.
The recall indicates a potential risk of kidney damage if blood and tissue fragments build up too quickly. The product is not safe to use without checking the model and lot numbers.
Check the model number and lot numbers on the tube. If it matches WA2PS20S with lot numbers starting with 154125, contact Trokamed for further instructions.
The affected tubes have the model number WA2PS20S and lot numbers starting with 154125. Check the product label for these identifiers.
We’ve drafted a message you can send Trokamed to request your refund or repair — edit it as you like.
Subject: Recall Z-0713-2025 — Trokamed Trokamed Hello, I own a Trokamed that is covered by recall Z-0713-2025 from Trokamed. 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.
