Reported Feb 1, 2023 · Ongoing
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation
Teleflex LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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?
- Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation
- Lot codes and dates
6 of 6 products
Products covered by this recall Model / number Barcodes Product as published 17006004026704319558Batch Number: KME21E1411, UDI: (01)04026704319558(17)260428(10)KME21E1411 1700700402670431957204026704319572Batch Number (UDI): KME21D1430 ((01)04026704319572(17)260328(10)KME21D1430), KME21E1290 ((01)04026704319572(17)260428(10)KME21E1290) 17007504026704319589Batch Number: KME21D1785, UDI:(01)04026704319589(17)260328(10)KME21D1785 1700800402670431959604026704319596Batch Number (UDI): KME21D1204 ((01)04026704319596(17)260328(10)KME21D1204), KME21E1287 ((01)04026704319596(17)260428(10)KME21E1287) 1700854026704319602Batch Number: KME21E1296, UDI:(01)4026704319602(17)260428(10)KME21E1296 1700904026704319619Batch Number: KME21E1232, UDI: (01)4026704319619(17)260428(10)KME21E1232 - Amount recalled
- 2,270 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Potential for pilot balloon non-inflation or cuff non-deflation.
This product could cause temporary or reversible health problems — stop using it.
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