Loading...
Loading...
All product recalls associated with TELEFLEX LLC.
Total Recalls
20
Past Year
0
Class I (Serious)
0
Most Recent
May 2023
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
Teleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that restricts the application of the clip to the applier. With this step feature missing on the cartridge, the clip is mounted in a more variable position, allowing the clips to load farther back in the clip applier jaw grooves. This may potentially result in inappropriate or inadequate clip application to vascular structures.
The product contains an expired diluent vial. If the impacted product is used, the sterility of the diluent component cannot be assured as it has passed beyond the studied shelf life of the product.
Potential for pilot balloon non-inflation or cuff non-deflation.
Potential for pilot balloon non-inflation or cuff non-deflation.
Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
Product may not be sterile
Incidents of device splitting or detaching during use
Incidents of device splitting or detaching during use
Incidents of device splitting or detaching during use
Incidents of device splitting or detaching during use