13 results
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13ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
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KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver
FDA Recall
Open, Classified
·Pro-Dex Inc·Product code GEY·February 15, 2023
KLS Martin Battery Pack, REF: KLS BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver 2.0 surgical driver, REF: KLS-SD-2000
FDA Recall
Open, Classified
·Pro-Dex Inc·Product code MOQ·September 23, 2024
KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter.
FDA Recall
Open, Classified
·Pro-Dex Inc·Product code GET·February 14, 2023
Laser light show projectors manufactured by BLS, Model PURE 5000/10000.
FDA Recall
Open, Classified
·Beyond Laser Systems, LLC·Product code REA·June 30, 2025
Laser light show projectors manufactured by BLS, Model DIODE 1000/2000/3000.
FDA Recall
Open, Classified
·Beyond Laser Systems, LLC·Product code REA·June 30, 2025
Laser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000.
FDA Recall
Open, Classified
·Beyond Laser Systems, LLC·Product code REA·June 30, 2025
MOSAIQ Oncology Information System
FDA Recall
Open, Classified
·Elekta, Inc.·Product code IYE·May 21, 2026
LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo RD rainbow Adt 8 SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF 11996-000515 Masimo LNCS-II rainbow DCI 8 SpCO, Adult Reusable Sensor REF 11996-000519 Masimo LNCS-II rainbow DCI 8 SpCO, Pediatric Reusable Sensor REF 11996-000520 The LIFEPAK 15 Monitor/Defibrillator (LP15) is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. RD rainbow" 8 SpCO sensors are indicated for the continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2), pulse rate, carboxyhemoglobin saturation (SpCO), and methemoglobin saturation (SpMet) for use with adult, pediatric, infant, and neonatal patients during both no motion and motion conditions, and for patients who are well or poorly perfused in hospitals, hospital-type facilities, mobile, and home environments.
FDA Recall
Open, Classified
·Physio-Control, Inc.·Product code MKJ·January 21, 2025
VIDAS CLINICAL VIDAS PROGESTERONE 60 TESTS, CATALOG 30409-01
FDA Recall
Open, Classified
·Biomerieux Inc·Product code JLS·November 9, 2022
VIDAS PRG Progesterone, REF 30409-01
FDA Recall
Open, Classified
·bioMerieux, Inc.·Product code JLS·September 22, 2021
Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module and retrofitted with IndiGo Drive Assistance modules
FDA Recall
Open, Classified
·ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ul. Ks. Piotra Wawrzyniaka 2 Komorniki Poland·Product code FNL·August 29, 2023
Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module and retrofitted with IndiGo Drive Assistance modules
FDA Recall
Open, Classified
·ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ul. Ks. Piotra Wawrzyniaka 2 Komorniki Poland·Product code FNL·August 29, 2023
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
FDA Recall
Open, Classified
·ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ul. Ks. Piotra Wawrzyniaka 2 Komorniki Poland·Product code FSA·March 10, 2026