Recall archive / FDA device enforcement
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181050 — FDA record Z-1873-2023
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date May 25, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181050
- Reason
- Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- Classification
- Class I
- Recalling firm
- TELEFLEX LLC
- Quantity
- 54469 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1873-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | 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 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US Nationwide distribution including Puerto Rico.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Jul 5, 2023
- Recall initiation date
- May 25, 2023
- Center classification date
- Jun 29, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.