RUSCH Slick Set Cuffed Endotracheal Tubes with specific REF and lot numbers recalled due to potential cuff inflation while pilot balloon remains flat.
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
Teleflex Medical Europe Ltd recalls specific RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Sets. The hazard involves the tube cuff possibly inflating while the pilot balloon stays flat, which could lead to improper airway management during medical procedures.
The endotracheal tube cuff may inflate while the pilot balloon remains flat. This can cause improper airway sealing, potentially leading to air leaks or inadequate ventilation during medical procedures.
Healthcare professionals using the recalled RUSCH Slick Set tubes for intubation procedures are most at risk. Patients undergoing medical procedures with these tubes could face complications if the cuff inflates incorrectly.
Check for RUSCH Slick Set Cuffed Endotracheal Tubes with REF numbers 170050, 170055, 170060, 170065, 170070, 170075, 170080, 170085, 170090, or 170095. Also look for specific lot numbers listed in the recall notice.
Identify the reference number and lot number on the tube packaging to confirm if it is recalled.
The recall is due to reports that the endotracheal tube cuff could inflate while the pilot balloon remained flat, potentially causing improper airway management during medical procedures.
The official recall notice does not specify a remedy for this product, so healthcare providers should check the product details and contact Teleflex Medical Europe Ltd for further guidance.
Yes, specific lot numbers for each reference number are listed in the recall notice. Check the reference numbers and lot numbers provided in the recall details.
We’ve drafted a message you can send RUSCH to request your refund or repair — edit it as you like.
Subject: Recall Z-2319-2021 — RUSCH RUSCH Hello, I own a RUSCH that is covered by recall Z-2319-2021 from RUSCH. 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.
