medical HIGH RISK Updated 2023-07-05

TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasa

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Recalled Product

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085

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Hazard / Issue

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI/DI 4026704319602, Batch Numbers: 18FG09, 18GG20, 18GG28, 18HG07, 18JG11, 18KG18, 19AG37, 19CT32, 19DT02, 19ET38, 19ET60, 19HT61, 19HT66, 19IT44, 19KT21, 19KT55, 19LT32, 20AT32, 20BT05, 20BT23, 20CT51, 20GG36, KME20L0398, KME20L2376, KME20M3247, KME21C0298, KME21E1296, KME21K1876, KME21L0573, KME22F0484

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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