Bruder Healthcare Company, LLC - Bruder Thermalon - Class 2 Recall
Thermalon Sinus Compress (French), Item Number 24332F (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
Randox Laboratories Ltd. - Cystatin C Calibrator - Class 2 Recall
Cystatin C Calibrator - In vitro diagnostic (IVD) use in the calibration of the Randox Cystatin C assay on automated analysers Catalog Number: CVS 2699 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
Bio-Rad Laboratories - BioRad, QXDx BCRABL IS Kit - Class 2 Recall
Bio-Rad, REF: 12005660, QXDx BCR-ABL %IS Kit (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
Olympus Corporation of the Americas - InstaClear Lens Cleaner - Class 2 Recall
InstaClear Lens Cleaner-indicated for use during routine diagnostic procedures and during endoscopic sinus surgery. Model Number: LCS1500UNOL LCS1800UNST LCS4K00UNOL LCS1530BTOL LCS1830BTST LCS4K30BTOL LCS1530TPOL LCS1830TPST LCS4K30TPOL LCS1545BTOL LCS1845BTST LCS4K45BTOL LCS1545TPOL LCS1845TPST LCS4K45TPOL LCS1570BTOL LCS1870BTST LCS4K70BTOL LCS1570TPOL LCS1870TPST LCS4K70TPOL (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
Hologic, Inc. - Aptima CMV Quant Assay - Class 2 Recall
Aptima CMV Quant Assay, Reference numbers: AW-22600-001, AW-25509-001, and AW-26381-001 Amplification Reagent, Enzyme Reagent, Promoter Reagent, Amplification Reconstitution Solution, Enzyme Reconstitution Solution, Promoter Reconstruction solution, Target capture Reagent, Reconstitution Collars. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
Alcon Research, LLC - Alcon Custom Pak Surgical Procedure Pack - Class 2 Recall
SYRINGE,BULB,2OZ/60CC,GREEN, Part: 300055070, packaged inside Alcon Custom-Pak Surgical Procedure Packs, Products: 18018-06, 3865-44, 5675-76, 13554-11, 18018-06, 15190-16 , 15190-16, 15190-16, 15190-16, 15190-16, 13554-11, 5918-39, 15190-16, 15190-16, 9208-66, 9208-66, 5675-76, 5918-39, 9208-66, 15190-16, 9065-25, 5918-39, 16066-15, 16066-15 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
Ortho-Clinical Diagnostics - VITROS Chemistry Products Performance Verifier - Class 2 Recall
VITROS Performance Verifier II (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
Ortho-Clinical Diagnostics - VITROS Chemistry Products Performance Verifier - Class 2 Recall
VITROS Performance Verifier I (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
Thoratec Corp. - HeartMate III Left Ventricular Assist System - Class 1 Recall
HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemption (IDE) 2. HeartMate 3TM Sealed Outflow Graft with Bend Relief, US 3. HeartMate 3TM Sealed Outflow Graft with Bend Relief, OUS 4. HeartMate 3 LVAS Implant Kit, IDE 5. HeartMate 3TM LVAS Implant Kit, US 6. HeartMate 3TM LVAS Implant Kit, OUS HeartMate 3"Left Ventricular Assist System: The HeartMate 3 LVAS is a set of equipment and materials that together comprise a medical device designed to provide therapeutic benefit to those affected with advanced heart failure. In service, the LVA...
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
Thoratec Corp. - HeartMate II Left Ventricular Assist System - Class 1 Recall
HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate IITM Sealed Outflow Graft with Bend Relief REF 103393 2. HeartMate IITM LVAS Implant Kit, US REF 106015 3. HeartMate IITM LVAS Implant Kit, OUS REF 106016 Update (February 14, 2024) HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II¿ LVAS Implant Kit, OUS REF 102139 2. HeartMate II¿ LVAS Implant Kit, US REF 1355 3. HeartMate II¿ LVAS Implant Kit (with RSOC Controller), US REF 103695 4. HeartMate II¿ LVAS Implant Kit (with RSOC Controller), OUS REF 103693 5. HeartMate II¿ LVAS Implant Kit (with Sealed Graft), US REF 1...
Source: Medical Device Recalls - March 23, 2024 Category: Medical Devices Source Type: alerts
ConvaTec, Inc - Convatec EsteemBody - Class 2 Recall
Convatec EsteemBody Soft Convex, Drainable Pouch, Product codes (REF): a) 423643, b) 423658, c) 423659, d) 423664, e) 423666, f) 423645, g) 423667, h) 423657, i) 423652, j) 423646, k) 423654, l) 423653, m) 423647, n) 423644, o) 423648, p) 423665, q) 423656, r) 423651, s) 423660, t) 423661 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 22, 2024 Category: Medical Devices Source Type: alerts
Covidien - Situate Laparotomy Sponge - Class 2 Recall
Situate Laparotomy Sponge, RF and X-ray Detectable, REF: L1818-04P01C-1 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 22, 2024 Category: Medical Devices Source Type: alerts
ARROW INTERNATIONAL Inc. - ARROW QuickFlash - Class 1 Recall
ARROW QuickFlash Radial Artery Catherization (wire, guide, catheter), Part Numbers: a) REF AK-04220; b) REF ASK-04220-FMH1; c) REF ASK-04220-HHC; d) REF ASK-04220-KSP; e) REF ASK-04220-PSU; f) REF ASK-04220-UCL1; g) REF ASK-04500-AH; h) REF ASK-04500-HF-S; i) REF NA-04220-S1A; j) REF NA-04220-X1A; k) REF RA-04220; l) REF RA-04220-W (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 22, 2024 Category: Medical Devices Source Type: alerts
Angiodynamics, Inc. - Class 2 Recall
MINI STICK MAX 4F X 10 CM STD .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-749 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 22, 2024 Category: Medical Devices Source Type: alerts
Angiodynamics, Inc. - Class 2 Recall
MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759 (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 22, 2024 Category: Medical Devices Source Type: alerts
