🔍 RecallPedia

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120

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 14026704644879, Batch Numbers: 18JG23, 18JG26, 18JG34, 18KG26, 18LG05, 19AG18, 19AG21, 19AG24, 19AG37, 19BG01, 19BG04, 19BG07, 19BG12, 19BG16, 19CT58, 19CT71, 19DT06, 19DT20, 19ET77, 19FT14, KME20H0975, KME20H0976, KME20J0324, KME20K0771, KME20K2545, KME20K2568, KME20L0627, KME21A1886, KME21B1671, KME21B2506, KME21C2475, KME21D0447, KME21K1723, KME22A0056, KME22B0179, KME22B0180, KME22B0181, KME22B0464, KME22C2255, KME22C2256, KME22D1638, KME22D1639, KME22D1788, KME22E1489, KME22F1500, KME22F1669, KME22F1670, KME22G3099, KME22H3107, KME22H3275, KME22J2354, KME22J2355, KME22J2356, KME23A2360
  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:

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120

Product Codes/Lot Numbers:

UDI/DI 14026704644879, Batch Numbers: 18JG23, 18JG26, 18JG34, 18KG26, 18LG05, 19AG18, 19AG21, 19AG24, 19AG37, 19BG01, 19BG04, 19BG07, 19BG12, 19BG16, 19CT58, 19CT71, 19DT06, 19DT20, 19ET77, 19FT14, KME20H0975, KME20H0976, KME20J0324, KME20K0771, KME20K2545, KME20K2568, KME20L0627, KME21A1886, KME21B1671, KME21B2506, KME21C2475, KME21D0447, KME21K1723, KME22A0056, KME22B0179, KME22B0180, KME22B0181, KME22B0464, KME22C2255, KME22C2256, KME22D1638, KME22D1639, KME22D1788, KME22E1489, KME22F1500, KME22F1669, KME22F1670, KME22G3099, KME22H3107, KME22H3275, KME22J2354, KME22J2355, KME22J2356, KME23A2360

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1837-2023

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