Teleflex, Inc.

FDA recalling firm · 3 enforcement events · 11 product records · 2014–2014 · PA

Teleflex, Inc. has 3 FDA enforcement events on this register (11 product records) between 2014 and 2014: 3 device; the busiest year was 2014 with 3.

33% of its events are Class I; the most common class is Class II (2). 0 events are listed as ongoing; the recalling firm's address is in PA.

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
12 Dec 2014	R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is required following intubation.	Device	Class II	1	Terminated
4 Dec 2014	MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and humidify gases…	Device	Class I	1	Terminated
21 Nov 2014	Bronchial Double Lumen Tube Set (Left), Sterile	Device	Class II	9	Terminated

By type and class

Device3

Class II2

Class I1

Class I: 33% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Teleflex, Inc. by year initiated.

Questions and answers

How many FDA recalls has Teleflex, Inc. had?

3 enforcement events (11 product records) on this register, 2014–2014: 3 device.

Are any Teleflex, Inc. recalls ongoing?

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

What class are Teleflex, Inc. recalls?

2 Class II, 1 Class I. 33% 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.