Manufacturer
11 recalls in our database name Teleflex, Inc. as the manufacturing or recalling firm.
Of the 11 recalls from Teleflex, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (9%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Teleflex is recalling sterile Tracheopart Sets because the cobb connector may detach from the main connector before use.
Teleflex is recalling Bronchial One Lumen Tubes - Left because customer complaints reported the cobb connector detaching from the main connector prior to use.
Teleflex is recalling specific lots of Bronchial Double Lumen Tube Sets because the cobb connector may detach from the main connector before use.
Teleflex is recalling Carlens Bronchial Double Lumen Tube Sets because the cobb connector may detach from the main connector before use.
Teleflex is recalling Bronchial One Lumen Tubes because the cobb connector may detach from the main connector prior to use.
Teleflex is recalling sterile Tracheopart Sets because the cobb connector may detach from the main connector before use.
Teleflex is recalling specific batches of Bronchial Double Lumen Tube Sets because the cobb connector may detach from the main connector before use.
Teleflex, Inc. is recalling White Bronchial Double Lumen Tube Sets (Right) Sterile because the cobb connector may detach from the main connector prior to use.
Teleflex is recalling sterile Bronchial Double Lumen Tube Sets because the cobb connector may detach from the main connector before use.
Teleflex is recalling RUSCH Curved Reinforced Endotracheal Tubes because the labeled cuff diameter does not match the actual cuff diameter, though the actual product meets specifications.
Teleflex is recalling 18 MAQUET Servo Humidifier 163 units because connector mount cracks may cause leaks, potentially depriving patients of adequate anesthetic gases.
Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.
Teleflex
American medical device company
Source: Wikidata (Q7696143), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.