Teleflex Medical recalls Pilling Sump-Suction Tube model REF 351547 with missing internal tip. This device may not function as intended. Affected units have lot numbers A8, C8, or I7.
The internal tip is missing from the device, causing the device to not function as intended.
Teleflex Medical is recalling Pilling Sump-Suction Tubes with model reference 35154: the internal tip is missing, so the device may not work properly. This could affect medical use, especially in critical care settings.
The internal tip is missing, so the tube cannot function as intended. This could lead to improper drainage of fluids, potentially causing complications during medical procedures.
Healthcare professionals using the Pilling Sump-Suction Tube for medical procedures are most at risk. Patients receiving care through this device may be affected if the tube fails.
Check for the model reference 351547 on the tube. Affected units have lot numbers A8, C8, or I7. This product was sold with these specific batch numbers.
Look for the model reference 351547 on the tube to confirm if it is affected.
The recall states the internal tip is missing, causing the device to not function as intended. This could lead to improper drainage during medical procedures.
The recall does not specify a remedy, so check the model and lot numbers to determine if it is affected.
Check for model reference 351547 and lot numbers A8, C8, or I7.
We’ve drafted a message you can send Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0846-2019 — Teleflex Medical Teleflex Medical Hello, I own a Teleflex Medical that is covered by recall Z-0846-2019 from Teleflex 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
