TERRASIL BED SORE AND PRESSURE SORE RELIEF (allantoin) ointment [Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions]
Updated Date: Fri, 01 Dec 2023 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 1, 2023 Category: Drugs & Pharmacology Source Type: alerts
TRIDERMA PRESSURE SORE RELIEF (calendula officinalis) cream [Genuine Virgin Aloe Corporation]
Updated Date: Fri, 03 Feb 2023 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 3, 2023 Category: Drugs & Pharmacology Source Type: alerts
ISHANCARE BED AND PRESSURE SORE ointment [Hunan Xiong Shi Pharmaceutical Co., Ltd]
Updated Date: Mon, 03 Oct 2022 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 3, 2022 Category: Drugs & Pharmacology Source Type: alerts
Stryker Medical Division of Stryker Corporation - Class 2 Recall
IsoGel Air - support surface assists in the prevention and treatment of all pressure ulcers stages, Model Number 2860, Part 2860000999 (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 7, 2021 Category: Medical Devices Source Type: alerts
Stryker Medical Division of Stryker Corporation - Class 2 Recall
Proform- support surface is used to assist in the prevention and treatment of all categories/stages of pressure ulcers, Model Number: 2710, Part #¿2710000027¿¿¿¿ (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 7, 2021 Category: Medical Devices Source Type: alerts
TERRASIL BED SORE AND PRESSURE SORE RELIEF (calendula officinalis flower, thuja occidentalis whole) ointment [Aidance Skincare & Topical Solutions, LLC]
Updated Date: Mon, 07 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 7, 2020 Category: Drugs & Pharmacology Source Type: alerts
Hill-Rom, Inc. - Progressa Bed - Class 2 Recall
Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Percussion/Vibration Therapy. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 31, 2020 Category: Medical Devices Source Type: alerts
Hill-Rom, Inc. - Centrella Smart Bed - Class 2 Recall
Centrella Smart+ Bed, Catalog No. P7900 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Percussion/Vibration Therapy. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 31, 2020 Category: Medical Devices Source Type: alerts
KCI USA, INC. - Negative Pressure Wound Therapy Powered Suction Pump - Class 2 Recall
ACTIV.A.C Therapy System; Model Numbers; US: 340000 ACTIV.A.C., NORTH AMERICAN UDI (01)00878237008188 - Product Usage: is an integrated wound management system for use in the acute, extended, and home care settings. When used on open wounds, it is intended to create an environment that promotes wound healing by secondary or tertiary (delayed primary) intention by preparing the wound bed for closure, reducing edema, promoting granulation tissue formation and perfusion, and by removing exudate and infectious material. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 10, 2020 Category: Medical Devices Source Type: alerts
Gentell, Inc - Gentell Hydrogel Ag - Class 2 Recall
Gentell Hydrogel Ag 4x4, model no. GEN-11420 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 6, 2020 Category: Medical Devices Source Type: alerts
Gentell, Inc - Gentell Hydrogel Ag - Class 2 Recall
Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 6, 2020 Category: Medical Devices Source Type: alerts
Gentell, Inc - Gentell Hydrogel Ag - Class 2 Recall
Gentell Hydrogel Ag 2x2, model no GEN-11220 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 6, 2020 Category: Medical Devices Source Type: alerts
Gentell, Inc - Gentell Hydrogel Ag - Class 2 Recall
Gentell Hydrogel Ag 4oz. Tube, model no. - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Silver Antimicrobial Wound Dressing is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 6, 2020 Category: Medical Devices Source Type: alerts
Degania Silicone, Ltd. - Smith & Nephew Negative Pressure Wound Therapy 15FR Channel Wound Drain - Class 2 Recall
Smith & Nephew Negative Pressure Wound Therapy 15FR Channel Wound Drain PN: 02872 An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels, drain fluids from body cavities, or evaluate certain physiologic conditions. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 13, 2019 Category: Medical Devices Source Type: alerts
Medela Inc - Invia Motion Negative Pressure Wound Therapy System. - Class 2 Recall
Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure Wound Therapy (Model 087.4010); b. 15 Days Negative Pressure Wound Therapy (Model 087.4012); c. 60 Days Negative Pressure Wound Therapy (Model 087.4014) Product Usage: The Invia Motion Negative Pressure Wound Therapy (NPWT) system is indicated for patients who would benefit from a suction device (NPWT) as it creates an environment that promotes wound healing by secondary or tertiary (delayed primary) intention by preparing the wound bed for closure, reducing edema, promoting granulation tissue formation and perfusion, and by r...
Source: Medical Device Recalls - July 24, 2018 Category: Medical Devices Source Type: alerts
