Teleflex Magill Endotracheal Tubes Recalled for Connector Disconnection Risk
Teleflex LLC is recalling 1,670 Magill endotracheal tubes (REF 100380055) due to reports of 15mm connector disconnection. The Class I recall affects units 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 is an FDA Class I recall, which requires a minimum severity score of 4 per FDA classification criteria. No reported illnesses, injuries, or deaths are documented in the source material, preventing a higher classification.
Plain-English summary
Teleflex LLC is recalling approximately 1,670 Magill endotracheal tubes (oral/nasal, uncuffed/plain, REF 100380055) with UDI/DI 14026704340672. The affected batch numbers are: 19ET11, 19GT51, 19JT20, 20AT13, KME20H2315, KME21A2778, KME22A0155, KME22A2335, KME22E0288, KME22E1272, and KME22F1551.
The recall was issued as an FDA Class I recall due to reports of disconnection of the 15mm connector from the endotracheal tube. The affected units were distributed nationwide in the United States, including Puerto Rico.
The recalled product
- Product
- Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380055
- 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 (12)
- UDI/DI 14026704340672
- Batch Numbers: 19ET11
- 19GT51
- 19JT20
- 20AT13
- KME20H2315
- KME21A2778
- KME22A0155
- KME22A2335
- KME22E0288
- KME22E1272
- KME22F1551
Distribution
Distributed nationwide across the United States.
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