TELEFLEX LLC

FDA recalling firm · 9 enforcement events · 140 product records · 2022–2026 · NC

TELEFLEX LLC has 9 FDA enforcement events on this register (140 product records) between 2022 and 2026: 9 device; the busiest year was 2022 with 4.

22% of its events are Class I; the most common class is Class II (7). 8 events are listed as ongoing; the recalling firm's address is in NC.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
7 May 2026	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…	Device	Class II	1	Ongoing
25 May 2023	Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor	Device	Class II	3	Ongoing
25 May 2023	Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050	Device	Class I	123	Ongoing
28 Apr 2023	Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or tissue ligation	Device	Class II	1	Ongoing
12 Apr 2023	Teleflex (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.	Device	Class II	1	Ongoing
8 Dec 2022	Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation	Device	Class II	3	Ongoing
28 Sep 2022	Pilling Wecksorb Cylindrical Sponges	Device	Class II	1	Terminated
20 Sep 2022	Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116). Urinary catheter.	Device	Class II	1	Ongoing
29 Aug 2022	Iso-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.	Device	Class I	6	Ongoing

By type and class

Device9

Class II7

Class I2

Class I: 22% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for TELEFLEX LLC by year initiated.

Questions and answers

How many FDA recalls has TELEFLEX LLC had?

9 enforcement events (140 product records) on this register, 2022–2026: 9 device.

Are any TELEFLEX LLC recalls ongoing?

8 events are listed as ongoing in the current openFDA export.

What class are TELEFLEX LLC recalls?

7 Class II, 2 Class I. 22% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.