Endotracheal Tube Connector Disconnection Hazard in Teleflex Slick Set
Teleflex is recalling Slick Set Uncuffed Endotracheal Tube kits due to reports of 15mm connector disconnection. 20,662 units have been distributed nationwide, including Puerto Rico.
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 Class I recalls score at minimum 4 per the rubric. The source reports connector disconnection without reported injuries or deaths, supporting a Severe classification.
Plain-English summary
Teleflex LLC is recalling the Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 170135) for oral and nasal use. The recall follows reports of disconnection of the 15mm connector from the endotracheal tube. The FDA classified this as a Class I recall.
20,662 units of the product have been distributed nationwide, including Puerto Rico. The affected devices are identified by UDI/DI code 14026704647030 and batch numbers from 18KG03 through KME22H2625.
The recalled product
- Product
- Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135
- Manufacturer
- TELEFLEX LLC
- Category
- Medical Device — Respiratory
- Hazard
- Affected units
- 20,662
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 14026704647030
- Batch Numbers: 18KG03
- 18KG07
- 18KG18
- 18LG22
- 19AG18
- 19AG21
- 19AG24
- 19AG37
- 19BG04
- 19BG12
- 19BG40
- 19CT49
- 19CT58
- 19DT06
- 19DT20
- 19DT38
- 19ET22
- 19ET28
- 19GT45
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.
See all 123 products in this recall →Related recalls
Same manufacturer · TELEFLEX LLC
See all →- HighPilling Wecksorb Neurosponges Surgical Sponges Recalled for Endotoxin Contamination
FDA (Devices) · 2026-07-08
- HighTeleflex Pilling Surgical Retractor Recalled for Incomplete Cleaning Instructions
FDA (Devices) · 2023-07-12
- ModerateTeleflex Surgical Retractor Recalled for Incomplete Pre-Cleaning Instructions
FDA (Devices) · 2023-07-12
- ModerateTeleflex Pilling O'Reilly Esophageal Retractor Recalled for Incomplete Cleaning Instructions
FDA (Devices) · 2023-07-12
- SevereEndotracheal Tubes Recalled for Potential 15mm Connector Disconnection
FDA (Devices) · 2023-07-05
Same hazard · connector disconnection
See all →- SevereTeleflex Endotracheal Tubes: FDA Recalls 1110 Units for Connector Disconnection
FDA (Devices) · 2023-07-05
- SevereFDA Recalls Slick Set Uncuffed Endotracheal Tubes for Connector Disconnection
FDA (Devices) · 2023-07-05
- SevereFDA Recalls Teleflex Endotracheal Tubes for Connector Disconnection
FDA (Devices) · 2023-07-05
- SevereRUSCHELIT Safety Clear Tracheal Tube 15mm connector disconnection risk nationwide recall
FDA (Devices) · 2023-07-05
- SevereTeleflex Endotracheal Tubes Recalled Due to Connector Disconnection Risk
FDA (Devices) · 2023-07-05