Preformed AGT Endotracheal Tubes Recalled for Connector Disconnection
Teleflex is recalling 37,890 Preformed AGT endotracheal tubes due to reports of 15mm connector disconnection. The devices were distributed nationwide in the United States and 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 classification indicates serious health risk from endotracheal tube connector disconnection. Absence of reported deaths or serious injuries in the source text prevents a Critical rating.
Plain-English summary
Teleflex LLC is recalling 37,890 Preformed AGT Oral Endotracheal Tubes (REF 111781065) following reports that the 15mm connector can disconnect from the endotracheal tube. The devices are identified by UDI/DI 14026704341211. Multiple batch numbers are affected.
The recalled devices were distributed nationwide in the United States, including Puerto Rico. This is a Class I recall issued by the FDA.
Further information regarding remedies and recommendations should be obtained from Teleflex LLC or the FDA.
The recalled product
- Product
- Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781065
- Manufacturer
- TELEFLEX LLC
- Hazard
- connector-disconnection
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 14026704341211
- Batch Numbers: 18FG20
- 18FG31
- 18GG17
- 18HG21
- 18IG16
- 18IG30
- 18JG16
- 18JG20
- 18KG01
- 18LG30
- 19AG01
- 19AG25
- 19AG29
- 19BG18
- 19CG02
- 19DT35
- 19DT46
- 19ET36
- 19FT01
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- SevereMedline Spinal Block Kits Recalled for Data Integrity and Efficacy Issues
FDA (Devices) · 2026-06-03
- SevereAbiomed Automated Impella Controller recalled for motor control and pump failure risks
FDA (Devices) · 2026-06-03
- HighGE APEXPRO and CARESCAPE Telemetry Systems Risk Loss of Patient Monitoring
FDA (Devices) · 2026-06-03
- CriticalMedline spinal anesthetic kits recalled for quality and efficacy concerns
FDA (Devices) · 2026-06-03
- SevereMedline spinal anesthesia kits recalled for bupivacaine quality issues
FDA (Devices) · 2026-06-03