The Recall Desk
SevereFDA (Devices)·Z-1879-2023·Announced 2023-07-05

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
Category
Medical Device — Respiratory / Airway Management
Hazard
Affected units
446,163

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.

The notice also names 1 state specifically:

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.

See all 123 products in this recall →

Related recalls

Same manufacturer · TELEFLEX LLC

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Same hazard · connector disconnection

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