354 results · 25ms · Sources: EU EUDAMED, US FDA

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Dri-Sate Glacial Acidic Acid (liquid component of Dri-Sate Dry Acid Concentrate DR-240); 1 quart (0.95 liters); manufactured by Rockwell Medical Technologies, Inc., Grapevine, TX 76051.

FDA Recall
Terminated ·Rockwell Medical Technologies, Inc·Product code KPO·December 3, 2007

Oasis Dry Suction Water Seal Chest Drain, DRY SINGLE W/AC P/N: 3600-100

FDA Recall
Terminated ·Atrium Medical Corporation·Product code PAD·May 7, 2015

Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.

FDA Recall
Terminated ·Teleflex Medical·Product code KDQ·March 13, 2015

Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Product Number: 5999LPL, Exu-Dry Leg Dressing, Smith & Nephew, Inc.,Largo, Florida

FDA Recall
Terminated ·Smith And Nephew, Inc. Wound Management Division·Product code MCY·November 21, 2007

Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Product Number: 5999LV1, Exu-Dry Large Burn Vest, Smith & Nephew, Inc.,Largo, Florida

FDA Recall
Terminated ·Smith And Nephew, Inc. Wound Management Division·Product code MCY·November 21, 2007

Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Product Number: 5999BP1, Exu-Dry Adult Buttocks Dressing, Smith & Nephew, Inc.,Largo, Florida.

FDA Recall
Terminated ·Smith And Nephew, Inc. Wound Management Division·Product code MCY·November 21, 2007

Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Product Number : 5999MJ1, Exu-Dry Medium Burn Jacket, Smith & Nephew, Inc.,Largo, Florida.

FDA Recall
Terminated ·Smith And Nephew, Inc. Wound Management Division·Product code MCY·November 21, 2007

Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Product Number: 5999SJ1, Exu-Dry Small Burn Jacket , Smith & Nephew, Inc.,Largo, Florida.

FDA Recall
Terminated ·Smith And Nephew, Inc. Wound Management Division·Product code MCY·November 21, 2007

Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Product Number: 5999LJ1, Exu-Dry Large Burn Jacket, Smith & Nephew, Inc.,Largo, Florida

FDA Recall
Terminated ·Smith And Nephew, Inc. Wound Management Division·Product code MCY·November 21, 2007

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019

C7000 - CUSA Clarity Ultrasonic Tissue Ablation System

FDA Recall
Terminated ·Integra LifeSciences Corp.·Product code LFL·October 21, 2019