Teleflex, Inc.: 5 recalls on record
Recalls filed with 1 agency: FDA (5).
First recall on record: February 18, 2015. Most recent: August 26, 2015.
Risk classification: Class I: 1 · Class II: 4
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| August 26, 2015 | FDA | Carlens Bronchial Double Lumen Tube Set (Left) SterileZ-2411-2015 | Z-2411-2015 |
| August 26, 2015 | FDA | Bronchial One Lumen Tube - LeftZ-2409-2015 | Z-2409-2015 |
| August 26, 2015 | FDA | Bronchial Double Lumen Tube Set (Right), SterileZ-2408-2015 | Z-2408-2015 |
| February 25, 2015 | FDA | R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designat…Z-1124-2015 | Z-1124-2015 |
| February 18, 2015 | FDA | MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A h…Z-1008-2015 | Z-1008-2015 |
Questions about this company
- How many recalls does Teleflex, Inc. have?
- Recalert has 5 U.S. recalls on record for Teleflex, Inc., published between February 18, 2015 and August 26, 2015.
- What was the most recent Teleflex, Inc. recall?
- FDA recall Z-2411-2015, published August 26, 2015: Carlens Bronchial Double Lumen Tube Set (Left) Sterile
- Which agencies have handled Teleflex, Inc. recalls?
- Teleflex, Inc. appears as the recalling firm in recalls from: FDA (5).
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