Endotracheal Tubes Recalled for Connector Disconnection Risk
Teleflex LLC is recalling 11,188 endotracheal tubes due to reports of 15mm connector disconnection. The defect affects this critical airway management device nationwide.
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 recall requires minimum Severe rating (4). No deaths or serious injuries reported, preventing Critical (5) rating.
Plain-English summary
Teleflex LLC is recalling 11,188 units of Endotracheal Tube oral/nasal uncuffed/plain - Murphy (REF 100382045). The recall affects units distributed nationwide, including Puerto Rico.
The recall was issued following reports of disconnection of the 15mm connector from the endotracheal tube.
This is an FDA Class I recall. Multiple batch numbers are affected.
The recalled product
- Product
- Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045
- Manufacturer
- TELEFLEX LLC
- Hazard
- connector-disconnection
- airway-obstruction
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 14026704340825
- Batch Numbers: 18GG15
- 18GG26
- 18HG25
- 18IG04
- 18IG14
- 18IG29
- 18JG08
- 18JG35
- 18KG08
- 18LG01
- 19BG12
- 19DT13
- 19GT35
- 19KT13
- 19LT50
- 20CT11
- 20FT43
- 20GT22
- 20GT37
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- 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
- SevereMedline Spinal Trays Recalled Due to Quality and Efficacy Concerns
FDA (Devices) · 2026-06-03
- HighMedline Medical Convenience Kit Recalled: Wrong Syringe Type Inside
FDA (Devices) · 2026-06-03
- SevereMedline Spinal Block Kits Recalled for Data Integrity and Efficacy Issues
FDA (Devices) · 2026-06-03