Slick Set Uncuffed Endotracheal Tube Connector Disconnection Recall
Teleflex LLC is recalling approximately 10,650 units of Slick Set Uncuffed Endotracheal Tubes due to reports of 15mm connector disconnection from the tube.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Our severity reasoning: FDA classified this as Class I recall. Class I indicates reasonable probability that device use could cause serious adverse health consequences. Disconnection of a critical airway connector poses serious risk to ventilated patients.
Plain-English summary
Teleflex LLC is recalling approximately 10,650 units of the Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 170140) due to reports of disconnection of the 15mm connector from the endotracheal tube. An endotracheal tube with a disconnected connector could compromise ventilation and oxygen delivery to patients during medical procedures.
The affected units were distributed nationwide, including Puerto Rico. Multiple batch numbers are included in this recall. Healthcare providers should verify whether they have received affected units and contact Teleflex LLC regarding corrective actions.
The recalled product
- Product
- Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140
- Manufacturer
- TELEFLEX LLC
- Hazard
- connector-disconnection
- ventilation-failure
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- UDI/DI 14026704647047
- Batch Numbers: 18JG17
- 18JG32
- 18JG34
- 18KG29
- 18LG02
- 18LG15
- 18LG18
- 19AG09
- 19AG21
- 19BG12
- 19CT32
- 19DT06
- 19DT20
- 19ET38
- 19ET72
- 19ET77
- 19FT24
- 19JT29
- 20BG16
Distribution
Distributed nationwide across the United States.
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