FLUDEOXYGLUCOSE F-18 injection [Barbara Ann Karmanos Cancer Hospital]
Updated Date: Mon, 05 Apr 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - April 5, 2021 Category: Drugs & Pharmacology Source Type: alerts
FLUDEOXYGLUCOSE F 18 (fludeoxyglucose f-18) injection, solution [Massachusetts General Hospital]
Updated Date: Fri, 12 Mar 2021 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - March 12, 2021 Category: Drugs & Pharmacology Source Type: alerts
NYC HEALTH HOSPITALS HAND SANITIZER (ethyl alcohol) gel [Brands International]
Updated Date: Thu, 25 Feb 2021 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 25, 2021 Category: Drugs & Pharmacology Source Type: alerts
Getinge Group Logistics America, LLC - Getinge CM320 Series - Class 2 Recall
Getinge CM320 Series Washer Disinfector - Product Usage: A multi chamber washer disinfector intended for washing, disinfecting and drying of surgical instruments, containers, operating theatre shoes and operating theatre accessories normally used in hospitals and central disinfection facilities. The disinfected items must be further processed through terminal sterilization before use in any surgical procedure. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 17, 2021 Category: Medical Devices Source Type: alerts
FLUDEOXYGLUCOSE F-18 injection [Barbara Ann Karmanos Cancer Hospital]
Updated Date: Fri, 18 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 18, 2020 Category: Drugs & Pharmacology Source Type: alerts
Remote Diagnostic Technologies Ltd. - Tempus LSManual - Class 2 Recall
Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: The device is intended to be used in the following environmental: - Primarily in pre-hospital care and transport applications (including ambulances, fixed and rotary wing aircraft). (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 12, 2020 Category: Medical Devices Source Type: alerts
OXYGEN gas [Garrett County Memorial Hospital]
Updated Date: Thu, 10 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 10, 2020 Category: Drugs & Pharmacology Source Type: alerts
Philips North America Llc - Philips IntelliVue X2 - Class 2 Recall
Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport inside and outside of the hospital environment. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 9, 2020 Category: Medical Devices Source Type: alerts
Philips North America Llc - Philips IntelliVue MP2 - Class 2 Recall
Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport inside and outside of the hospital environment. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 9, 2020 Category: Medical Devices Source Type: alerts
Shimadzu Medical Systems - MobileDaRt Evolution - Class 2 Recall
Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan - Product Usage: The device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 5, 2020 Category: Medical Devices Source Type: alerts
Integra LifeSciences Corp. - Integra Padgett Dermatome Set - Class 2 Recall
Integra Padgett Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 12, 2020 Category: Medical Devices Source Type: alerts
Integra LifeSciences Corp. - Integra Padgett Electric Dermatome Set - Class 2 Recall
Integra Padgett Electric Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 12, 2020 Category: Medical Devices Source Type: alerts
Integra LifeSciences Corp. - 13 ft Handpiece Cable - Class 2 Recall
13 ft Handpiece Cable, component of the Dermatome Sets Model S and Model S6 and also as a spare part - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 12, 2020 Category: Medical Devices Source Type: alerts
Klarity Medical Products LLC - Klarity Vacuum Bags - Class 2 Recall
Klarity Vacuum Bags, Item Nos. R7504-30C, R7504-35BC,R7504-35C, R7644-32.5BC, RC7221-25BC, RC7504-17.5C - Product Usage: To be used by trained medical professionals for the stable support and positioning of patients undergoing external beam radiation therapy treatment in a clinic or hospital setting. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 25, 2020 Category: Medical Devices Source Type: alerts
Philips North America, LLC - Philips HeartStart MRx - Class 2 Recall
Philips HeartStart MRx, Monitor/Defibrillators with model numbers M3535A, M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9 - Product Usage: is intended for use in hospital and pre-hospital settings by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac life support or defibrillation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 14, 2020 Category: Medical Devices Source Type: alerts
