🔍 RecallPedia

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780080

Class I - Dangerous
🏥 Medical Devices Recalled: May 25, 2023 TELEFLEX Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI 14026704341129, Batch Numbers: 18FG33, 18GG23, 18GG34, 18HG30, 18IG11, 18IG18, 18JG21, 18JG35, 18KG19, 18KG41, 19AG15, 19BG04, 19BG19, 19GT65, 19HT68, 19IT15, 19LT21, 20AT26, 20CT12, 20CT13, 20CT32, 20DT35, 20FT19, KME20M3089, KME20M3090, KME21A1299, KME21A2090, KME21B0716, KME21B1783, KME21B1962, KME21B2204, KME21B2676, KME21C0599, KME22B0591, KME22C2317, KME22D0156, KME22D2122, KME22D2752, KME22E1153, KME22G0816, KME22H2094, KME22H2235, KME22H3271, KME22J0148, KME22J0532, KME22J3210, KME22K2844
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
TELEFLEX LLC
Reason for Recall:
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780080

Product Codes/Lot Numbers:

UDI/DI 14026704341129, Batch Numbers: 18FG33, 18GG23, 18GG34, 18HG30, 18IG11, 18IG18, 18JG21, 18JG35, 18KG19, 18KG41, 19AG15, 19BG04, 19BG19, 19GT65, 19HT68, 19IT15, 19LT21, 20AT26, 20CT12, 20CT13, 20CT32, 20DT35, 20FT19, KME20M3089, KME20M3090, KME21A1299, KME21A2090, KME21B0716, KME21B1783, KME21B1962, KME21B2204, KME21B2676, KME21C0599, KME22B0591, KME22C2317, KME22D0156, KME22D2122, KME22D2752, KME22E1153, KME22G0816, KME22H2094, KME22H2235, KME22H3271, KME22J0148, KME22J0532, KME22J3210, KME22K2844

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1948-2023

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