Medical DeviceMay 29, 2024
GMAX SYR 3ML/LL syringe recall — FDA Z-2108-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Latest records
Latest recalls — page 389
The newest recall records with useful source details are listed here.
Medical DeviceMay 29, 2024
MEDLINE SYR 10ML L/L recall — FDA Z-2047-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
Philips Ingenia 1.5T S Model Number (REF): 781347 recall — FDA Z-1847-2024
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceMay 29, 2024
Siemens Healthcare Diagnostics IMMULITE 2000 Anti-TG Ab Catalog # L2KTG6 (600 Tests), SMN recall — FDA Z-1887-2024
The potential for falsely elevated patient sample results when using impacted lots (785, 790, 791, and 793) of IMMULITE 2000 Anti-TG Ab.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceMay 29, 2024
MEDLINE SYR 20ML L/L WHITE SALINE recall — FDA Z-2086-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
FUJIFILM Healthcare Americas Noblus AC Adapter used with the Noblus Ultrasound Imaging recall — FDA Z-1884-2024
AC adapters of Noblus can heat up, and cause smoke in the worst case, when an excessive mechanical stress is applied to the socket for power cable (frequent insertion/removal of the power…
Class IIFDA: OngoingFUJIFILM Healthcare Americas Corporation
Medical DeviceMay 29, 2024
MEDLINE SYR 10ML L/L YELLOW CONT recall — FDA Z-2076-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
Philips Incisive CT - Computed Tomography X-Ray System intended to produce cross-sectional recall — FDA Z-1871-2024
Metal mounting box on the rotating scanner on rotor (heat change box) located within the Incisive CT system, may become compromised, resulting in potential contact with other gantry…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceMay 29, 2024
Siemens Healthcare Diagnostics IMMULITE 2000 Anti-TG Ab Catalog # L2KTG2 (200 Tests), SMN recall — FDA Z-1886-2024
The potential for falsely elevated patient sample results when using impacted lots (782, 783, 785, 786, 787, 788, 789, 790, 791, 792 and 793), of IMMULITE 2000 Anti-TG Ab.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceMay 29, 2024
Yamaha Surface Mounter YR series, YS series, i-Pulse series, Sigma series, S series, M recall — FDA Z-1815-2024
Non-medical laser products which were determined to not be in compliance with 21 C.F.R. ¿ 1010.2 in that they currently do not bear the required certification label.
Class IIFDA: OngoingYAMAHA MOTOR CORPORATION
Medical DeviceMay 29, 2024
MEDLINE SYR 10ML L/L RED LIDO recall — FDA Z-2079-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
GMAX SYR 60ML/LL Blue syringe recall — FDA Z-2123-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
MEDLINE SYR 3ML L/L GREEN recall — FDA Z-2055-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
Philips SmartPath to Ingenia Elition X - Magnetic Resonance (MR) systems are Medical recall — FDA Z-1863-2024
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceMay 29, 2024
MEDLINE SYR 20ML L/L WHITE recall — FDA Z-2070-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
MEDLINE SYR 5ML L/L BLUE recall — FDA Z-2059-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
GMAX SYR 5ML/LL syringe recall — FDA Z-2109-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
Philips Incisive CT - Computed Tomography X-Ray System intended to produce cross-sectional recall — FDA Z-1872-2024
Metal mounting box on the rotating scanner on rotor (heat change box) located within the Incisive CT system, may become compromised, resulting in potential contact with other gantry…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceMay 29, 2024
Philips SmartPath to dStream for XR and 3.0T- Magnetic Resonance (MR) systems are Medical recall — FDA Z-1862-2024
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceMay 29, 2024
Philips Ingenia 1.5T Model Number (REF): (1) 782140 recall — FDA Z-1845-2024
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceMay 29, 2024
Philips Upgrade dStream - Magnetic Resonance (MR) systems are Medical Electrical Systems recall — FDA Z-1865-2024
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceMay 29, 2024
MEDLINE SYR 10ML L/L BLUE SALINE recall — FDA Z-2078-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
Wolf Medical - WOLF-PAK DISPOSABLE SYRINGE 1 mL (cc) Luer Lock STERILE LATEX FREE NON recall — FDA Z-2101-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
Medical DeviceMay 29, 2024
GMAX SYR 12ML/LL syringe recall — FDA Z-2112-2024
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Class IIFDA: OngoingJiangsu Shenli Medical Production Co., Ltd.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories