Teleflex Endotracheal Tubes Recalled Due to Connector Disconnection
Teleflex is recalling 47,520 endotracheal tubes due to reported 15mm connector disconnection. The FDA classified this as a Class I recall; disconnected tubes could compromise airway management.
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 medical device recall for reported connector disconnection on critical airway management tubes. No deaths or serious injuries reported; minimum score of 4 per FDA Class I classification.
Plain-English summary
Teleflex LLC is recalling 47,520 units of Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff (REF 112082050). The tubes have been distributed nationwide including Puerto Rico.
The FDA received reports of disconnection of the 15mm connector from the endotracheal tube. These tubes are used for patient intubation and airway management in critical care settings. A connector disconnection could compromise ventilation during patient care.
The FDA classified this as a Class I recall. The affected units can be identified by UDI/DI 14026704341389 and specific batch numbers provided in the official FDA recall notice.
The recalled product
- Product
- Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050
- 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 14026704341389
- Batch Numbers: 18GG02
- 18GG19
- 18GG23
- 18GT06
- 18JG04
- 18JG15
- 18JG16
- 18JG18
- 18JT06
- 18JT16
- 19AG33
- 19AT20
- 19BG02
- 19BG03
- 19BG10
- 19BG15
- 19BG22
- 19BG26
- 19BG42
Distribution
Distributed nationwide across the United States.
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