Teleflex Endotracheal Tubes Recalled Due to Connector Disconnection
Teleflex LLC is recalling 7,800 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. The affected products were distributed nationwide in the US 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: This FDA Class I recall meets the criterion for Severe (4) because FDA Class I classification requires a minimum score of 4 per the rubric rules. No deaths or reported injuries have been documented, preventing a Critical (5) classification.
Plain-English summary
Teleflex LLC is recalling endotracheal tubes (ET tubes), model Murphy (REF 100382055). The recalled products are designed for oral or nasal use and are uncuffed.
The recall addresses reports of the 15mm connector disconnecting from the endotracheal tube.
Approximately 7,800 units with affected batch numbers were distributed nationwide in the United States and Puerto Rico.
The FDA has classified this as a Class I recall.
The recalled product
- Product
- Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055
- 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 14026704340849
- Batch Numbers: 18FG21
- 18FG33
- 18FT17
- 18FT31
- 18GT06
- 18HG06
- 18HG15
- 18IT06
- 18JG14
- 18JT12
- 18KG10
- 19AG05
- 19AT23
- 19BG10
- 19BG21
- 19BG26
- 19BT08
- 20CT47
- 20DT01
Distribution
Distributed nationwide across the United States.
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