[Recalled] Carlens Bronchial Double Lumen Tube Set (Left) Sterile — Customer complaints reporting that the cobb connector detached from the main co… | FDA 2014-11-21

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Customer complaints reporting that the cobb connector detached from the main connector prior to use.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Teleflex, Inc.

• Bronchial Double Lumen Tube Set (Right), Sterile — Class II
• 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 — Class I
• 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 intu — Class II
• Bronchial One Lumen Tube - Left — Class II
• Bronchial Double Lumen Tube Set (Left), Sterile — Class II
• Bronchial One Lumen Tube - Right — Class II

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.