Category

Medical Devices Recalls

15,654 medical devices recalls on record from CPSC, FDA, and USDA.

15,654 recalls
High RiskFDA
Baxter Healthcare Corporation
Baxter Flo-Rester, Disposable internal vessel occluder, distributed in the following sizes: a) Product Code 50100: 12MM, 1.00 MM GLOBAL...
Medical Devices·0 affected·Dec 6, 2023
High RiskFDA
Baxter Healthcare Corporation
PERI-GUARD SUPPLE, Product Codes: a) SPG1016: 10X16 CM US, TS; b) SPG0404: 4 X 4 CM US, TS; c) SPG0608: 6 X 8 CM US, TS; d) S...
Medical Devices·0 affected·Dec 6, 2023
High RiskFDA
Oakworks Inc
Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with Electric Access Back Sup...
Medical Devices·20 affected·Dec 5, 2023
CriticalFDA
Ambu Inc.
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
Medical Devices·11,845 affected·Dec 5, 2023
High RiskFDA
Shirakawa Olympus Co., Ltd.
Model No. CYF-V2, VISERA Cysto-Nephro Videoscope
Medical Devices·2,210 affected·Dec 4, 2023
CriticalFDA
Cardinal Health 200, Llc
Dover" IRRIGATION 1200 CC TRAY, 60 CC PISTON SYRINGE, STERILE SALINE, TIP PROTECTOR, ALCOHOL, LIDDED
Medical Devices·63,360 affected·Dec 4, 2023
CriticalFDA
Cardinal Health 200, Llc
TRACH KIT W/HYDROGEN & SALI
Medical Devices·661,560 affected·Dec 4, 2023
High RiskFDA
Olympus Corporation Of The Americas
Soltive SuperPulsed Laser System TFL Fiber Stripper, Model Numbers TFL-AFS150, TFL-AFS200, TFL-AFS365, TFL-AFS550, TFL-AFS940
Medical Devices·3,001 affected·Dec 4, 2023
High RiskFDA
Shirakawa Olympus Co., Ltd.
Model No. CYF-VH, CYSTO-NEPHRO VIDEOSCOPE
Medical Devices·4,780 affected·Dec 4, 2023
CriticalFDA
Cardinal Health 200, Llc
Dover" 100% SILICONE 400ML U/M TEMP SENSE FOLEY TRAY, LL, 18 FR (6.0 MM), 5CC, 2000ML DRAIN BAG, CSD
Medical Devices·36,300 affected·Dec 4, 2023
High RiskFDA
Shirakawa Olympus Co., Ltd.
Model No. CYF-VHR, CYSTO-NEPHRO VIDEOSCOPE
Medical Devices·1,547 affected·Dec 4, 2023
High RiskFDA
Shirakawa Olympus Co., Ltd.
Model No. BF-XP190, EVIS EXERA III Bronchovideoscope
Medical Devices·1,187 affected·Dec 4, 2023
High RiskFDA
Shirakawa Olympus Co., Ltd.
Model No. CYF-V2R, VISERA Cysto-Nephro Videoscope
Medical Devices·608 affected·Dec 4, 2023
CriticalFDA
Cardinal Health 200, Llc
Dover" 100% SILICONE FOLEY TRAY, LUER LOCK, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG, DRAIN SPOUT; Dover" 100% SILICONE 400 ML U/M FOLEY T...
Medical Devices·4,620 affected·Dec 4, 2023
CriticalFDA
Cardinal Health 200, Llc
Dover" HYDROGEL COATED LATEX 400 ML U/M FOLEY TRAY, LL, 14 FR (4.7 MM), 5 CC, 2000 ML DRAIN BAG, CSD; Dover" 100% SILICONE SILVER-HYDROG...
Medical Devices·7,800 affected·Dec 4, 2023
High RiskFDA
Shirakawa Olympus Co., Ltd.
Model No. CYF-5R, Cystonephrofiberscope
Medical Devices·2,551 affected·Dec 4, 2023
CriticalFDA
Cardinal Health 200, Llc
Dover URINE METER ADD-A-FOLEY TRAY, 200 ML, NEEDLE SAMPLING PORT, DRAIN TUBE, PREP TRAY; Dover UNIVERSAL TRAY, 1000 ML BASIN, PVP SWAB ST...
Medical Devices·435,060 affected·Dec 4, 2023
High RiskFDA
Shirakawa Olympus Co., Ltd.
Model No. BF-P190, EVIS EXERA III Bronchovideoscope
Medical Devices·2,600 affected·Dec 4, 2023
High RiskFDA
Howmedica Osteonics Corp.
Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for knee replacement Part Number: 72-16-0910
Medical Devices·9 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product Number: 6637-4-031
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Maquet Cardiovascular, Llc
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
Medical Devices·554 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-411
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-0110
Medical Devices·61 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-631
Medical Devices·0 affected·Dec 1, 2023
CriticalFDA
Olympus Corporation Of The Americas
SOLTIVE SuperPulsed Laser Fibers Model Numbers TFL-FBX150S, TFL-FBX200S, TFL-FBX365S, TFL-FBX550S, TFL-FBX940S, TFL-FBX150BS, TFL-FBX200BS
Medical Devices·82,200 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710
Medical Devices·118 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-2910
Medical Devices·16 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-2710
Medical Devices·36 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110
Medical Devices·107 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642-1-911
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026
Medical Devices·94 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0028
Medical Devices·52 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032
Medical Devices·70 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-028
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0030
Medical Devices·77 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-609
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-32J
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-0710
Medical Devices·269 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-0910
Medical Devices·192 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-611
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308
Medical Devices·1 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
TIBIAL BEARING INSERT SERIES P-S I ASSY Intended for knee replacement Product Number: 7291-0324
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-416
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-413
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7514
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-711
Medical Devices·0 affected·Dec 1, 2023
High RiskFDA
Howmedica Osteonics Corp.
HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-28J
Medical Devices·0 affected·Dec 1, 2023