TELEFLEX MEDICAL INC: 9 recalls on record

Recalls filed with 1 agency: FDA (9).

First recall on record: February 19, 2020. Most recent: June 1, 2022.

Risk classification: Class I: 3 · Class II: 6

Most recent recalls

DateAgencyProduct
June 1, 2022FDA(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex…Z-1126-2022
February 23, 2022FDAArrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W c…Z-0625-2022
February 23, 2022FDAArrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-WC …Z-0626-2022
August 12, 2020FDAPleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A-8000I-06 - Product Usage: CHEST…Z-2749-2020
August 5, 2020FDARusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: T…Z-2726-2020
August 5, 2020FDARusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) - Product Usage: T…Z-2731-2020
February 26, 2020FDAPilling Aortic Punch, 4.0 mm Standard Tip, REF 353440Z-1269-2020
February 19, 2020FDAHUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kitZ-1114-2020
February 19, 2020FDARusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic SystemZ-1117-2020

Questions about this company

How many recalls does TELEFLEX MEDICAL INC have?
Recalert has 9 U.S. recalls on record for TELEFLEX MEDICAL INC, published between February 19, 2020 and June 1, 2022.
What was the most recent TELEFLEX MEDICAL INC recall?
FDA recall Z-1126-2022, published June 1, 2022: (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-sterile; (3) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/Swivel, Product #190…
Which agencies have handled TELEFLEX MEDICAL INC recalls?
TELEFLEX MEDICAL INC appears as the recalling firm in recalls from: FDA (9).

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