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Teleflex, Inc.

Complete recall history across all FDA and CPSC categories — 11 total recalls

Teleflex, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (11)

FDA medical device enforcement actions by Teleflex, Inc.

Date Product Reason Class
Dec 12, 2014 R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube... Teleflex Medical has issued an advisory notification for the RUSCH Curved Rei... Class II
Dec 4, 2014 MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-81... Connector mount cracks which may lead to a leak failure during use and necess... Class I
Nov 21, 2014 Tracheopart Set (Left), Sterile Customer complaints reporting that the cobb connector detached from the main ... Class II
Nov 21, 2014 White Bronchial Double Lumen Tube Set (Right) Sterile Customer complaints reporting that the cobb connector detached from the main ... Class II
Nov 21, 2014 Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile Customer complaints reporting that the cobb connector detached from the main ... Class II
Nov 21, 2014 Tracheopart Set (Right), Sterile Customer complaints reporting that the cobb connector detached from the main ... Class II
Nov 21, 2014 Bronchial One Lumen Tube - Right Customer complaints reporting that the cobb connector detached from the main ... Class II
Nov 21, 2014 Bronchial Double Lumen Tube Set (Left), Sterile Customer complaints reporting that the cobb connector detached from the main ... Class II
Nov 21, 2014 Bronchial One Lumen Tube - Left Customer complaints reporting that the cobb connector detached from the main ... Class II
Nov 21, 2014 Bronchial Double Lumen Tube Set (Right), Sterile Customer complaints reporting that the cobb connector detached from the main ... Class II
Nov 21, 2014 Carlens Bronchial Double Lumen Tube Set (Left) Sterile Customer complaints reporting that the cobb connector detached from the main ... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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