Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181050
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 14026704340566, Batch Numbers: 18FG31, 18FT35, 18GG23, 18GT32, 18HG17, 18JG19, 18JG21, 18JG37, 18KG18, 18KG19, 18KG21, 18KG38, 18KG39, 18LG14, 19AG01, 19BG02, 19BG18, 19CG01, 19CG02, 19CT28, 19DT05, 19DT30, 19DT35, 19ET36, 19ET39, 19ET40, 19ET61, 19ET69, 19FT01, 20AT26, 20DT18, KME21A2039, KME21B2623, KME21C0543, KME21C1149, KME21C3398, KME21C3399, KME21D1236, KME21F0888, KME21L2303, KME21L2790, KME21M2313, KME21M2314, KME21M2317, KME21M2318, KME21M2380, KME21M2481, KME22A0760, KME22A2297, KME22B0755, KME22B2679, KME22C0412, KME22C2194, KME22C2195, KME22D1145, KME22D2262, KME22D3177, KME22F1334, KME22F2203, KME22F3000, KME22F3239, KME22F3241
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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 uncuffed/plain - Murphy, REF 100181050
Product Codes/Lot Numbers:
UDI/DI 14026704340566, Batch Numbers: 18FG31, 18FT35, 18GG23, 18GT32, 18HG17, 18JG19, 18JG21, 18JG37, 18KG18, 18KG19, 18KG21, 18KG38, 18KG39, 18LG14, 19AG01, 19BG02, 19BG18, 19CG01, 19CG02, 19CT28, 19DT05, 19DT30, 19DT35, 19ET36, 19ET39, 19ET40, 19ET61, 19ET69, 19FT01, 20AT26, 20DT18, KME21A2039, KME21B2623, KME21C0543, KME21C1149, KME21C3398, KME21C3399, KME21D1236, KME21F0888, KME21L2303, KME21L2790, KME21M2313, KME21M2314, KME21M2317, KME21M2318, KME21M2380, KME21M2481, KME22A0760, KME22A2297, KME22B0755, KME22B2679, KME22C0412, KME22C2194, KME22C2195, KME22D1145, KME22D2262, KME22D3177, KME22F1334, KME22F2203, KME22F3000, KME22F3239, KME22F3241
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1873-2023
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