Teleflex recalls

Teleflex has 151 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 8 Jul 2026. 139 are still ongoing. 1 was reported in the last 12 months.

Total recalls151since 2015
Last 12 months1reported
Class I13086% of total
Ongoing139latest 8 Jul 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 130 86%Class II 21 14%Class III 0 0%

Why teleflex is recalled

By year

Ongoing teleflex recalls

139 active

All teleflex recalls, newest first

151 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIPilling Wecksorb Neurosponges recalled by TeleflexTeleflexDevice MalfunctionNationwide
DeviceCLASS IIPilling Lowsley Prostatic Tractor Str recalled by TeleflexTeleflexOtherNationwide
DeviceCLASS IIPilling O'reilly Esophageal Retractor recalled by TeleflexTeleflexOtherNationwide
DeviceCLASS IIPilling Lowsley Prostatic Tractor Cvd recalled by TeleflexTeleflexOtherNationwide
DeviceCLASS ISlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide
DeviceCLASS IPreformed AGT Oral Endotracheal Tube Murphy Eye recalled by TeleflexTeleflexOtherNationwide
DeviceCLASS IPreformed AGT Oral Endotracheal Tube Murphy Eye recalled by TeleflexTeleflexOtherNationwide
DeviceCLASS ISlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide
DeviceCLASS IEndotracheal Tube oral/nasal Murphy Eye, High Volume recalledTeleflexOtherNationwide
DeviceCLASS IPreformed AGT Oral Endotracheal Tube Murphy Eye recalled by TeleflexTeleflexOtherNationwide
DeviceCLASS IRuschelit Safety Clear Tracheal Tube, oral/nasal, Magill recalledTeleflexOtherNationwide
DeviceCLASS ISlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide
DeviceCLASS IPreformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy recalledTeleflexOtherNationwide
DeviceCLASS IFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide
DeviceCLASS ISlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide
DeviceCLASS IEndotracheal Tube oral/nasal uncuffed/plain - Magill recalledTeleflexOtherNationwide
DeviceCLASS IPreformed AGT Oral Endotracheal Tube Murphy Eye recalled by TeleflexTeleflexOtherNationwide
DeviceCLASS IEndotracheal Tube oral/nasal Murphy Eye, High Volume recalledTeleflexOtherNationwide
DeviceCLASS IFlexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide
DeviceCLASS IEndotracheal Tube oral/nasal uncuffed/plain - Magill recalledTeleflexOtherNationwide
DeviceCLASS IPreformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy recalledTeleflexOtherNationwide
DeviceCLASS IEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff recalledTeleflexOtherNationwide
DeviceCLASS IEndotracheal Tube oral/nasal uncuffed/plain - Murphy recalledTeleflexOtherNationwide
DeviceCLASS IPreformed AGT Oral Endotracheal Tube Murphy Eye recalled by TeleflexTeleflexOtherNationwide
DeviceCLASS IFlexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide
DeviceCLASS ISlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide
DeviceCLASS IPreformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy recalledTeleflexOtherNationwide
DeviceCLASS IFlexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide
DeviceCLASS IPreformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy recalledTeleflexOtherNationwide
DeviceCLASS ISlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal recalledTeleflexOtherNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.