Slick Set Endotracheal Tubes Recalled for Connector Disconnection
Teleflex is recalling 870 units of Slick Set Uncuffed Endotracheal Tubes nationwide due to reports of disconnection of the 15mm connector from the tube.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: FDA classified this as a Class I recall. The severity rubric specifies that Class I recalls indicate a serious hazard with potential for serious adverse health consequences, which places this recall in the Severe category.
Plain-English summary
Teleflex LLC is recalling 870 units of the Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 150030) following reports of disconnection of the 15mm connector from the endotracheal tube. The affected products were distributed nationwide, including Puerto Rico.
Affected batch numbers are 18IG15, 18IG21, 18IG27, 18JG02, and 18JG14 (UDI/DI 4026704319664). Healthcare providers and facilities using these products should contact Teleflex for more information.
The recalled product
- Product
- Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150030
- Manufacturer
- TELEFLEX LLC
- Hazard
- Affected units
- 870
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 (6)
- UDI/DI 4026704319664
- Batch Numbers: 18IG15
- 18IG21
- 18IG27
- 18JG02
- 18JG14
Distribution
Part of a larger recall action
This product is one of 123 recalled by TELEFLEX LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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