BEUDAMED
    22 results · 11ms · Sources: EU EUDAMED, US FDA

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    iQ200 Series Urine Microscopy Analyzer: a) iQ 200 Select, Part Numbers C10684 and 700-3345; b) iQ 200 Elite, Part Numbers C10683 and 700-3375; in-vitro diagnostic device, urine analysis, c) iQ200 Select 1500, Part Number 700-3347, d) iQ200 Sprint, Part Number 700-3325

    FDA Recall
    Open, Classified ·Beckman Coulter, Inc.·Product code KQO·April 5, 2023

    Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Sensititre Aris HIQ system YV4000-VZ

    FDA Recall
    Open, Classified ·Remel, Inc·Product code LRG·February 12, 2025

    Atrium Pneumostat Chest Drain Valve, Part Number 16100

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code KDQ·August 26, 2021

    DeRoyal SafeLiner Suction Canister, 1000cc, REF PHESL-1000B

    FDA Recall
    Open, Classified ·DeRoyal Industries Inc·Product code KDQ·February 9, 2023

    Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two boxes. One box includes 50 eaches of liners in a poly bag and the second box includes 50 eaches of lids in a poly bag. For OR530H, the customer receives the number of liners and lids purchased in one case without the individual boxes. The "H" denotes a single quantity when being ordered.

    FDA Recall
    Open, Classified ·Medline Industries Inc·Product code KDQ·January 31, 2019

    The Ocean Water Seal Chest Drain is a plastic, three bottle vacuum collection device. It consists of a collection chamber that holds shed mediastinal blood, a water seal chamber using a water seal that prevents air from entering into the pleural space and a suction control chamber, which incorporates a mechanical regulator to control suction pressures imposed upon the patient's pleural cavity.

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code KDQ·October 22, 2021

    Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code KDQ·October 18, 2022

    Express Mini 500 Dry Seal Chest Drain, Part Number 16400

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code KDQ·March 1, 2023

    LINER, SOFT, SUCTION CANISTER, 1500CC, REF OR929K

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code KDQ·March 22, 2024

    1,5L MED-SOFT SINGLE LINER WITH SOLIDIFIER, REF OR1920PG

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code KDQ·March 22, 2024

    Atrium Oasis Dry Suction Water Seal Chest Drain, Part Number: 3600-100, DRAIN, OASIS SINGLE W/AC, 3600 SINGLE COLLECTION.

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code KDQ·September 5, 2023

    Atrium Pneumostat Chest Drain Valve, Part Number 16100

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code KDQ·March 1, 2023

    LINER, SOFT, SUCTION CANISTER, 1500CC, REF DYNDSCL1500

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code KDQ·March 22, 2024

    1,5L MED-SOFT LINER W/ 6MMX3M TUB. & ADULT VC, REF OR53929

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code KDQ·March 22, 2024

    Medline Semi-rigid suction liners labeled as follows: a) SEMI RIGID SUCTION LINER, REF OR515; b) SEMI RIGID SUCTION LINER WITH TUBING, REF OR526K; c) SEMI RIGID SUCTION LINER WITH TUBING, REF OR527K; d) SEMI RIGID SUCTION LINER WITH TUBING, REF OR529K

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code KDQ·June 27, 2024

    Pleur-Evac Adult-Ped Wet, LF Intl Eng, product code: A-8000I - Product Usage: CHEST DRAINAGE: To evacuate air and/or fluid from the chest cavity or mediastinum. To help prevent air and/or fluid from re-accumulating in the chest cavity or mediastinum. To help re-establish and maintain normal intra-thoracic pressure gradients. To facilitate complete lung re-expansion to restore normal breathing dynamics.

    FDA Recall
    Open, Classified ·TELEFLEX MEDICAL INC·Product code KDQ·June 30, 2020

    1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code KDQ·March 22, 2024

    1,5L MED-SOFT LINER W/ 6MMX1,8M TUB. & ADULT VC, REF OR53926

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code KDQ·March 22, 2024

    Medline medical procedure kits labeled as follows: a) KIT CANISTER SUCT W 12FT, REF DYKM2169

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code KDQ·March 22, 2024

    GETINGE USA SALES LLC OCEAN Chest Drain System Atrium 2100 mL Model Number: 2002-000

    FDA Recall
    Open, Classified ·Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233·Product code KDQ·May 25, 2022