Teleflex Preformed AGT Endotracheal Tubes Connector Disconnection Recall
Teleflex is recalling approximately 446,163 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. The connector failure could affect tube function during patient 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. Per the rubric, FDA Class I recalls warrant a minimum severity score of 4 (Severe). The 15mm connector disconnection could compromise endotracheal tube function during patient care.
Plain-English summary
Teleflex LLC is recalling approximately 446,163 units of the Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff (REF 111781045) nationwide, including Puerto Rico.
The recall is due to reports of disconnection of the 15mm connector from the endotracheal tube. This connector is essential for proper tube function and airway management.
Healthcare facilities should verify batch numbers against the official recall list and discontinue use of affected devices. Contact Teleflex for instructions on replacement or return.
The recalled product
- Product
- Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781045
- 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 14026704341174
- Batch Numbers: 18FG33
- 18GG16
- 18HG17
- 18HG21
- 18HG29
- 18HG30
- 18HG31
- 18IG10
- 18IG14
- 18IG17
- 18IG20
- 18JG02
- 18JG03
- 18JG16
- 18JG19
- 18JG20
- 18JG35
- 18JG37
- 18KG01
Distribution
Distributed nationwide across the United States.
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