🔍 RecallPedia

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045

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 14026704340825, Batch Numbers: 18GG15, 18GG26, 18HG25, 18IG04, 18IG14, 18IG29, 18JG08, 18JG35, 18KG08, 18LG01, 19BG12, 19DT13, 19GT35, 19KT13, 19LT50, 20CT11, 20FT43, 20GT22, 20GT37, KME20H0783, KME20J2818, KME20J2819, KME20J2846, KME20K0469, KME20M1075, KME21B0085, KME21B1134, KME21B1828, KME21C1577, KME21C2244, KME21C2444, KME21D2950, KME21D2951, KME22D2158, KME22D2478, KME22E0295, KME22E0608, KME22E0909, KME22E0911, KME22E1313, KME22E2291, KME22J3174, KME22K2663, KME22K2686, KME22M0003, KME22M1623, KME23A2310, KME23B0782
  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:

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045

Product Codes/Lot Numbers:

UDI/DI 14026704340825, Batch Numbers: 18GG15, 18GG26, 18HG25, 18IG04, 18IG14, 18IG29, 18JG08, 18JG35, 18KG08, 18LG01, 19BG12, 19DT13, 19GT35, 19KT13, 19LT50, 20CT11, 20FT43, 20GT22, 20GT37, KME20H0783, KME20J2818, KME20J2819, KME20J2846, KME20K0469, KME20M1075, KME21B0085, KME21B1134, KME21B1828, KME21C1577, KME21C2244, KME21C2444, KME21D2950, KME21D2951, KME22D2158, KME22D2478, KME22E0295, KME22E0608, KME22E0909, KME22E0911, KME22E1313, KME22E2291, KME22J3174, KME22K2663, KME22K2686, KME22M0003, KME22M1623, KME23A2310, KME23B0782

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1936-2023

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