Richard Wolf recalls TEM Tube Sets with small diameter tube material that may cause improper use during transanal endoscopic procedures. Affected units include Lot 32324159, Model 4170.801.
Tube material of a smaller diameter was used.
Richard Wolf is recalling TEM tube sets that use a smaller diameter tube material. This could lead to improper use during transanal endoscopic procedures. Affected units have specific lot and model numbers.
The tube material has a smaller diameter than intended, which could lead to improper use during transanal end:oscopic procedures. This might cause issues with the procedure's effectiveness or safety.
Medical professionals performing transanal endoscopic microsurgery (TEM) using the recalled tube sets are most at risk. Patients undergoing these procedures with the affected equipment may also be impacted.
Check for Lot Number 32324159 and Model # 4170.801 on the tube set packaging. The product is designed for transanal endoscopic microsurgery procedures.
Look for Lot Number 32324159 and Model # 4170.801 on the tube set packaging.
The tube material has a smaller diameter than intended, which could lead to improper use during transanal endoscopic procedures.
Lot Number 32324159, Model # 4170.801
The recall does not specify a stop-use instruction, so you can continue using it if it's not the affected model or lot.
We’ve drafted a message you can send Richard Wolf to request your refund or repair — edit it as you like.
Subject: Recall Z-2706-2020 — Richard Wolf Richard Wolf Hello, I own a Richard Wolf that is covered by recall Z-2706-2020 from Richard Wolf. 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.
