Preformed AGT Oral Endotracheal Tube Connector May Disconnect
Teleflex LLC is recalling Preformed AGT Oral Endotracheal Tubes due to reported connector disconnections. The recall affects 24,752 units 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: This is an FDA Class I recall, which the agency's classification indicates is a serious issue. Although no illnesses or injuries are reported in the source text, the reported connector disconnections from endotracheal tubes—which are critical for patient airway management—present a significant risk of harm that justifies the Class I designation.
Plain-English summary
Teleflex LLC is recalling Preformed AGT Oral Endotracheal Tubes (uncuffed/plain - Murphy, REF 100181055) due to reports that the 15mm connector may disconnect from the endotracheal tube. This recall affects 24,752 units distributed nationwide in the United States, including Puerto Rico.
The disconnection of the connector from the endotracheal tube poses a significant risk because these tubes are critical for maintaining a patient's airway during medical procedures. A disconnection could interrupt oxygen delivery and require immediate corrective action by medical staff.
The affected products are identified by UDI/DI 14026704340573 and specific batch numbers listed in the FDA recall notice. Healthcare facilities should identify affected units using their batch numbers and consult Teleflex LLC or their medical device representative for guidance on appropriate corrective actions.
The recalled product
- Product
- Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181055
- 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 14026704340573
- Batch Numbers: 18FT35
- 18GG18
- 18GG23
- 18GT32
- 18IG16
- 18JG35
- 18KG01
- 18KG39
- 18LG15
- 18LG18
- 18LG39
- 19AG01
- 19AG25
- 19CG02
- 19CT33
- 19DT05
- 19DT35
- 19ET36
- 19ET61
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