Reported Jul 5, 2023 · Ongoing
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504585
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?
- Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504585
- Lot codes and dates
- UDI/DI 4026704547647
- Batch Numbers
73 of 73 codes
18FG1318FG1518FG2518GG2018GG2818HG1218HG1918IG0618IG2718JG0218JG2318JG2618KG1818KG2319AG0519AG3119AG3719CT1719CT5819CT7119DT0219ET3219ET4519FT1419FT2419GT5219HT6119HT8019IT3919KT1719KT4819LT5020AT3220AT5320BT0520CT1220CT4420DT0920DT3720GG2720GG4520GT38KME20H0532KME20J2404KME20J2405KME20K2625KME20L0624KME20L1482KME20L2303KME20L2832KME21E1295KME21K1874KME21M1728KME21M2447KME21M2519KME22B0987KME22B1754KME22B2155KME22C0679KME22C0866
- Amount recalled
- 56640 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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