Reported Jul 5, 2023 · Ongoing
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781055
Teleflex LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: TELEFLEX LLC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437
Is this the product you have?
- Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781055
- Lot codes and dates
- UDI/DI 14026704341198
- Batch Numbers
169 of 169 codes
18FT3518FT3918GG1718GG1818GT3218IG1018IG1618IG1718JG1318JG2018JG3518JG3718KG1818KG3918KG4118LG1218LG1418LG3018LG3919AG2919BG0319BG0419BG1819BG1919BG3319CG0119CG0219CG0419CT2819CT3319CT5619DT0319DT3019DT3519DT4219DT4619ET1619ET3419FT0119GT6319HT3119HT5519IT0119IT1219IT1419IT1519IT1919KT0219KT4119LT1720BT0120BT0220CT0720DT1820DT2920DT3220ET3420ET4920FT1820FT64
- Amount recalled
- 172721 units
This recall covers 123 products
The agency filed one notice per product. You are reading one of them; the other 122 are below.
110 more are in the archive.
Where it was sold
- Nationwide
- PR
Why it was recalled
Stop using this product now
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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