Recall Register

TELEFLEX LLC: FDA recalls

FDA enforcement events from 2022 to 2026; export dated . The recall start date and FDA report date are separate fields. Read the recall classes.

FDA enforcement reports name TELEFLEX LLC as the recalling firm in 9 events. The events have 140 product records. The recalls started from 2022 to 2026. All the events are device recalls. By FDA enforcement events, TELEFLEX LLC is number 386 of 1,628 firms that have a page. Events that TELEFLEX LLC started: none in 2024 and none in 2025. For all FDA enforcement events, the count rose by 3.6%, from 1,773 in 2024 to 1,836 in 2025. Class I is 22.2% of its events and 17.7% of all FDA events.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

9 events, newest first.

FDA enforcement events of TELEFLEX LLC
InitiatedProduct (first record)TypeClassRecordsStatus
7 May 2026Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling Wecksorb Neurosponge Strips (Cotton) Model/Catalog Number: 200100 200101 200102 200103 200104 200105 200106 200108 200110 200112 200120 200121 200123 200131 Software Version: N/A Product Description: Wecksorb Neurosponges are…DeviceClass II1Ongoing
25 May 2023Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractorDeviceClass II3Ongoing
25 May 2023Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050DeviceClass I123Ongoing
28 Apr 2023Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or tissue ligationDeviceClass II1Ongoing
12 Apr 2023Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000; for sealing residual oozing of tissue tracts of femoral access sites that have been previously closed by suture/collagen-based hemostatic devices.DeviceClass II1Ongoing
8 Dec 2022Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubationDeviceClass II3Ongoing
28 Sep 2022Pilling Wecksorb Cylindrical SpongesDeviceClass II1Terminated
20 Sep 2022Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116). Urinary catheter.DeviceClass II1Ongoing
29 Aug 2022Iso-Gard Filter S, REF : a) 19211, OUS only; b) 19212; Microbial medical gas filter, single-use. Bacterial/viral filters for use in breathing system for the protection of patient and equipment.DeviceClass I6Ongoing

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

TELEFLEX LLC: events for each product type
TypeEvents
Device9
TELEFLEX LLC: events in each class
ClassEvents
Class II7
Class I2
Share of the events of the firm in Class I
22%
Share of all events on the register in Class I
18%
Events with the status Ongoing
8

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of TELEFLEX LLC, by the year that the recall started. The largest year is 2022, with 4 events.

Official channels

Cite this page

Recall Register. TELEFLEX LLC: FDA recalls. https://recallregister.com/firm/teleflex-llc/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
3 Nov 2026
State of the firm address
NC

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not rate one firm against another. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of TELEFLEX LLC have?
Class II: 7 events. Class I: 2 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of TELEFLEX LLC?
FDA event 98962, which the firm started on 7 May 2026. The first product in the record is: Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling Wecksorb Neurosponge Strips (Cotton) Model/Catalog Number: 200100 200101 200102 200103 200104 200105 200106 200108 200110 200112 200120 200121 200123 200131 Software Version: N/A Product Description: Wecksorb Neurosponges are…
How many FDA recalls of TELEFLEX LLC have the status Ongoing?
8 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.