DrugJul 24, 2024
Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, 100-count bottle recall — FDA D-0606-2024
CGMP Deviations
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
Latest records
Latest recalls — page 369
The newest recall records with useful source details are listed here.
VehicleJul 24, 2024
Tesla latch recall — NHTSA campaign 24V554000
Tesla, Inc. (Tesla) is recalling certain 2021-2024 Model 3, Model S, Model X, and 2020-2024 Model Y vehicles. The hood latch assembly may fail to detect an unlatched hood condition after…
latchTesla, Inc.
VehicleJul 23, 2024
Gulf States Toyota labels recall — NHTSA campaign 24V548000
Gulf States Toyota, Inc. (GST) is recalling certain Toyota 2023 GR Supra, 2024 4 Runner, Corolla, Grand Highlander, Grand Highlander Hybrid, Land Cruiser Hybrid, Tacoma, Tacoma Hybrid,…
labelsGulf States Toyota, Inc.
Medical DeviceJul 17, 2024
GE Vingmed Ultrasound As GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB recall — FDA Z-2316-2024
GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed…
Class IIFDA: OngoingGE Vingmed Ultrasound As
Medical DeviceJul 17, 2024
Maquet Cardiovascular The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed recall — FDA Z-2338-2024
There were 27 complaints between March 22, 2024, and April 30, 2024, related to VH-3500 and VH-4000, reporting that the C-Ring wire was straightened (due to insufficient bend radius) and…
Class IIFDA: OngoingMaquet Cardiovascular, LLC
Medical DeviceJul 17, 2024
ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator recall — FDA Z-2324-2024
G5 Semi-Automatic AED is shipped, with a protective film over its front panel, to protect the screen and shock button from cosmetic damage during shipping. It has come to our attention that…
Class IIFDA: OngoingZoll Medical Corporation
Medical DeviceJul 17, 2024
Fresenius Medical Care Holdings RTL190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor recall — FDA Z-2345-2024
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJul 17, 2024
Cardinal Health 200 Presource kits and trays, labeled as: 1) ANGIOGRAPHY PACK, Catalog recall — FDA Z-2327-2024
Cardinal Health is following the FDA's recommendations regarding the disposition of affected Jiangsu Shenli Medical Production Co. Ltd (Shenli) Syringes in the Merit Medical supplied…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJul 17, 2024
Fresenius Medical Care Holdings 191014: 2008K@HOME HD SYSTEM W/BIBAG (CANADA) - Blood Pump recall — FDA Z-2342-2024
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJul 17, 2024
Cardinal Health 200 Presource kits and trays, labeled as: 1) Cardiac Catheterization Kit recall — FDA Z-2328-2024
Cardinal Health is following the FDA's recommendations regarding the disposition of affected Jiangsu Shenli Medical Production Co. Ltd (Shenli) Syringes in the Merit Medical supplied…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJul 17, 2024
Pivotal Health Solutions Decompression Table Model E9011 recall — FDA Z-2326-2024
This product is being recalled due to potentially insufficient rework on a part (E7130-B) on the lumbar section of the frame on 6 distributed tables. There were 4 additional tables with the…
Class IIFDA: OngoingPivotal Health Solutions, Inc.
Medical DeviceJul 17, 2024
Fresenius Medical Care Holdings RTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood recall — FDA Z-2346-2024
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJul 17, 2024
Fresenius Medical Care Holdings 190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor recall — FDA Z-2341-2024
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJul 17, 2024
Echonous Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a recall — FDA Z-2325-2024
Ultrasound system has a bug in affected iOS software, which after DICOM export, can cause inaccuracy in postprocessed measurements done in 3rd party software, such as PACS or other…
Class IIFDA: OngoingEchonous Inc.
Medical DeviceJul 17, 2024
Baxter Healthcare VidiaPort carrying arm, mount for auxiliary products, model numbers: a) recall — FDA Z-2313-2024
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 17, 2024
Baxter Healthcare iLED 7 surgical lights, Model Numbers: a) 4068110 recall — FDA Z-2315-2024
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 17, 2024
Preat 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in recall — FDA Z-2318-2024
Due to incorrect milled titanium abutment being packaged and labeled.
Class IIFDA: OngoingPreat Corp
Medical DeviceJul 17, 2024
Fresenius Medical Care Holdings 190395: 2008K@HOME MACHINE, SHORT CAB,OLC/DP,HP - Blood Pump recall — FDA Z-2343-2024
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJul 17, 2024
Fresenius Medical Care Holdings 190904 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump recall — FDA Z-2340-2024
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJul 17, 2024
Fresenius Medical Care Holdings RTLR190395: 2008K@HOME MACHINE, SHORT CAB,OLC/DP,HP - Blood recall — FDA Z-2347-2024
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJul 17, 2024
Cardinal Health 200 Presource kits and trays, labeled as: 1) Neurological Tray, Catalog recall — FDA Z-2330-2024
Cardinal Health is following the FDA's recommendations regarding the disposition of affected Jiangsu Shenli Medical Production Co. Ltd (Shenli) Syringes in the Merit Medical supplied…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJul 17, 2024
Getinge Usa Sales ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B5 recall — FDA Z-2272-2024
The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate…
Class IIFDA: OngoingGetinge Usa Sales Inc.
Medical DeviceJul 17, 2024
SVS Non-sterile, single use, disposable gloves intended for medical purposes to be worn on recall — FDA Z-2320-2024
Firm received complaints regarding skin irritation when using the gloves, disintegration of the gloves when used with certain cleaning solutions, and mislabeled products (e.g., outer box…
Class IIFDA: OngoingSVS LLC
Medical DeviceJul 17, 2024
Baxter Healthcare Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 recall — FDA Z-2314-2024
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed…
Class IIFDA: OngoingBaxter Healthcare Corporation
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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