Teleflex Endotracheal Tube Recalled for Connector Disconnection Risk
Teleflex LLC is recalling 670 endotracheal tubes due to reports that the 15mm connector is disconnecting from the tube. Affected units were 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: FDA Class I medical device recall, which indicates serious potential for adverse health consequences. An endotracheal tube is critical to airway management; connector disconnection could compromise its function and patient safety.
Plain-English summary
Teleflex LLC is recalling 670 endotracheal tubes (Magill model, High Volume, Low Pressure Cuff, REF 112080090) distributed nationwide in the United States including Puerto Rico. The recall is due to reports of the 15mm connector disconnecting from the affected tubes.
An endotracheal tube is a medical device used in airway management. Disconnection of the connector from the tube could compromise its function.
Affected units have batch numbers 18FT24, 18FT26, 19ET83, 19GT29, 19KT58, and 19KT38. The device identifier (UDI/DI) is 14026704341266.
The recalled product
- Product
- Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080090
- Manufacturer
- TELEFLEX LLC
- Hazard
- Affected units
- 670
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 (7)
- UDI/DI 14026704341266
- Batch Numbers: 18FT24
- 18FT26
- 19ET83
- 19GT29
- 19KT58
- 19KT38
Distribution
Part of a larger recall action
This product is one of 123 recalled by TELEFLEX LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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