Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

6751–6775 of 39844

HighFDA (Devices)·Z-2229-2024·2024-07-10
Surgical Convenience Kits Recalled for Weak Seals Affecting Sterility
Medline Industries recalls 7,673 surgical convenience kits due to weak Pure Pouch seals that may compromise sterility. Kits were distributed nationwide to healthcare facilities.
Product
Nonsterile convenience kits: a. Medline Delivery, Pack #DYNJ901130I, containing a Pure Pouch with component Reorder #DYND04000, O.R. Scissors, S/B, 5.5 Sterile. b. Medline C-Section, Pack DYNJ902938J, containing a Pure Pouch with component Reorder #DYND04000, O.R. Scissor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2261-2024·2024-07-10
Stryker Corporation Recalls Expired Sterile Surgical Cannula Devices
Stryker Corporation has recalled expired sterile cannula devices distributed nationwide. The devices were past their expiration date, potentially compromising sterility and device safety.
Product
This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed once the cannula is placed. The electrode is then inserted into the cannula. Catalog Number: 0406-630-225
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2235-2024·2024-07-10
Surgical retractor blade manufacturing defect could cause bone fracture
SeaSpine Orthopedics is recalling Fathom Pedicle-Based Retractor C/C Blades due to manufacturing defects that could cause bone fracture. The recall affects 31 units distributed across nine US states.
Product
Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade, 50-80mm Model/Catalog Number: MR2102050 Product Description: Cranial Caudal Blade Component: Yes, a component of a retractor blade
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2265-2024·2024-07-10
Abbott Liberta RC Pulse Generator Unexpectedly Shuts Down Periodically
Abbott Liberta RC implantable pulse generators used for deep brain stimulation may unexpectedly turn off approximately every 50 days after activation, resulting in loss of therapy. Approximately 302 units have been recalled nationwide.
Product
Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2236-2024·2024-07-10
Acumatch L-Series Hip Implant Liners Recalled for Packaging Defect
Exactech is recalling Acumatch L-Series hip implant liners because some units were packaged without the specified protective ethylene vinyl alcohol (EVOH) layer, which is required for proper device protection.
Product
Acumatch L-Series BIPOLAR LINER, 22mm (BIPOLAR ENDOPROSTHESIS-Hip), Item Numbers: a) 100-22-19, SZ. L; b) 100-22-20, SZ. M; c) 100-22-21, SZ. N; d) 100-22-22, SZ. P; e) 100-22-23, SZ. R; f) 100-22-24, SZ. S; g) 100-22-25, SZ. T
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-2260-2024·2024-07-10
Stryker Curved Cement Delivery Needles Recalled: Expired Products Distributed
Stryker recalled its Curved Cement Delivery Needle (Lot 6659783) due to expired product distribution. Three units were distributed to customers in Arkansas, California, Colorado, Florida, and Michigan.
Product
Curved, super elastic cement delivery needle that passes through the cannula in a straight configuration and enters the vertebral body in a curved configuration. This provides physicians with the ability to inject bone cement into multiple different areas through a single point o
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2245-2024·2024-07-10
Medical Device Calibrator Kit Assigned Extended Incorrect Expiration Date
Ortho-Clinical Diagnostics is recalling a calibrator kit with an incorrect expiration date that could bias lab results if used past its true expiration date.
Product
VITROS Chemistry Products Calibrator Kit 29- In-Vitor used to calibrate the VITROS 5,1 FS/4600 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems for the quantitative measurement of total iron-binding capacity (TIBC) using VITROS Chemistry Products dTIBC Reagent Mo
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2233-2024·2024-07-10
Operating Room System Recalled for Incomplete Electrical Safety Testing Records
Olympus has recalled 227 EasySuite 4K operating room systems worldwide due to incomplete documentation of earth leakage testing, which is required to confirm electrical current levels are within safety standards.
Product
EasySuite 4K Integrated Operating Room System Model/Catalog Number: EasySuite 4K- The EasySuite 4K system includes a touch panel user interface for quick routing of 2K/4K procedural video to displays within the operating room and for convenient control of room video cameras, sur
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2243-2024·2024-07-10
WOM Tube Set for Irrigation Recalled Due to RFID Tag Data Error
WOM Tube Set for Irrigation (1700 units, Lots 4030902 and 4030903) is recalled due to incorrect RFID tag data that causes an error message preventing use in endoscopic surgeries, potentially resulting in surgical delays.
Product
WOM Tube Set for lrrlgatlon, single-use- Intended to transport irrigation fluid to the patient in endoscopic surgeries. Distr. by Endoscopy Smith & Nephew Inc. REF Numbers: T0449-01
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2140-2024·2024-07-03
Life2000 Ventilator systems recalled due to battery charging failure risk
The Life2000 Ventilator may fail to charge or experience intermittent charging behavior due to damage to the battery charger dongle. This FDA Class I recall affects approximately 2,510 units distributed nationwide.
Product
Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and BT-20-0002AP. The Life2000 ventilation system includes the Life2000 ventilator which has its individual label.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2159-2024·2024-07-03
Inspire Model 3028 Implantable Pulse Generator Manufacturing Defect
Inspire Medical Systems recalls the Model 3028 Implantable Pulse Generator due to a manufacturing defect causing electrical leakage and system malfunction that requires revision surgery. The recall affects 24 devices distributed in the US and Germany.
Product
Inspire Model 3028, IV Implantable Pulse Generator
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2164-2024·2024-07-03
Philips MR Torso Coil Recall: Potential Patient Burn Risk
Philips is recalling 307 SENSE XL TORSO COIL 3.0T units used in MR imaging systems worldwide due to potential for coils to overheat and cause patient burn injuries.
Product
SENSE XL TORSO COIL 3.0T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567394941, 453567394942, 453567394943, 453567394945, 459801593182. Coils may be included in kits with Mode Numbers: 989603050641, 98960
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2165-2024·2024-07-03
Philips SENSE XL Torso Coil 1.5T Recalled for Overheating Risk
Philips recalled 14 SENSE XL Torso Coils worldwide due to potential overheating. The coils could heat up during use and cause patient burn injuries.
Product
SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567502281, 453567502282, 453567502283, 453567502284, 453567502285, 453567502286, 459801585212.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2163-2024·2024-07-03
Philips SENSE XL TORSO COIL Recall Due to Potential Patient Burn Hazard
Philips is recalling SENSE XL TORSO COIL units used in MRI imaging because the coils may heat up excessively and cause patient burns. This FDA Class I recall affects 729 units distributed worldwide.
Product
SENSE XL TORSO COIL 1.5T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567141882, 453567141883. Coils may be included in kits with Mode Numbers: 989603014351 & 989603014352.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2212-2024·2024-07-03
Medtronic Implantable Defibrillators Recalled for Manufacturing Weld Defect
Medtronic is recalling 82 implantable cardioverter defibrillators due to a manufacturing defect involving weld cracks discovered during quality control testing before distribution to patients.
Product
Product not distributed in the US. Implantable Cardioverter Defibrillators: a. VIVA QUAD XT CRT-D, Model Number DTBA2QQ. b. CLARIA MRI CRT-D SureScan, Model Number DTMA2D1. c. CLARIA MRI QUAD CRT-D SureScan, Model Number DTMA2QQ. d. AMPLIA MRI CRT-D SureScan, Mod
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2195-2024·2024-07-03
Medtronic Implantable Defibrillator Recalled for Manufacturing Weld Defect
Medtronic recalls 26 units of CROME HF QUAD CRT-D implantable defibrillators worldwide due to weld cracks discovered during manufacturing quality control. Devices were contained before reaching patients.
Product
CROME HF QUAD CRT-D MRI SureScan, Model Number DTPC2QQ, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2187-2024·2024-07-03
X-ray table recalled for fire hazard from power supply unit short circuit
Siemens MULTIX TOP I PRO X-ray tables are recalled due to a power supply short circuit that may cause overheating and fire. Three units have been identified.
Product
MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 475525
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2200-2024·2024-07-03
Medtronic PRIMO MRI DR SureScan Cardioverter Defibrillators Recalled for Manufacturing Defect
Medtronic is recalling two PRIMO MRI DR SureScan implantable cardioverter defibrillators due to a potential manufacturing defect involving weld cracks detected during manufacturing quality testing.
Product
PRIMO MRI DR SureScan, Model Number DDMD3D1, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2194-2024·2024-07-03
Medtronic COBALT XT Heart Devices Recalled Due to Manufacturing Defect
Medtronic is recalling 58 COBALT XT HF QUAD implantable cardioverter defibrillators worldwide due to a weld crack manufacturing defect that caused devices to fail quality checks.
Product
COBALT XT HF QUAD CRT-D MRI SureScan, Model Number DTPA2QQ, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2186-2024·2024-07-03
Siemens Multix TOP X-ray Table Recalled Due to Fire Risk
Siemens is recalling 3 Multix TOP I PRO radiographic X-ray tables due to a short circuit in the Touch Display power supply unit that may cause overheating and fire.
Product
MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number:475517
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2202-2024·2024-07-03
Implantable Cardioverter Defibrillator Recalled Due to Manufacturing Weld Defect
Medtronic is recalling 26 MIRRO MRI DR SureScan Implantable Cardioverter Defibrillators due to a manufacturing defect involving a weld crack that could affect device function.
Product
MIRRO MRI DR SureScan, Model Number DDME3D4, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2216-2024·2024-07-03
NovaGuide 2 Ultrasound Systems Recalled for Electrical Shock Risk
FDA is recalling 45 NovaGuide 2 Intelligent Ultrasound systems due to a defective grounding cable that could become disconnected and cause electrical shock, electrical interference, or equipment malfunction.
Product
NovaGuide 2 Intelligent Ultrasound, REFs: NSC-NVGSYS2 & NSC-NVGSYS2-CA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2196-2024·2024-07-03
Medtronic EVERA S VR Implantable Cardioverter Defibrillator Recalled for Manufacturing Defect
Medtronic is recalling EVERA S VR implantable cardioverter defibrillators due to a potential manufacturing defect involving a weld crack that can cause device failure. The defect was identified during manufacturing leak testing.
Product
EVERA S VR, Model Number DVBC3D1, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2172-2024·2024-07-03
CARESCAPE Patient Monitors May Not Power On After Battery Replacement
Certain GE CARESCAPE patient monitors may fail to power on after mains power loss during battery maintenance, potentially delaying recognition of patient condition changes.
Product
CARESCAPE B850 Model Numbers: a) MBC303, Model Numbers: 1) 2078633-001, 2) 2078633-010, 3) 2078633-012, 4) 2078633-017, 5) 2078633-028, 6) 2095802-001-54069330, 7) 2095802-001-554922, 8) 2095802-001-554923, 9) 2095802-001-554924, 10) 2095802-001-554925, 11) 2095802
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2203-2024·2024-07-03
Implantable Cardioverter Defibrillator Recalled for Manufacturing Weld Defect
Medtronic recalls 46 PRIMO MRI VR SureScan implantable cardioverter defibrillators due to a manufacturing defect. Weld cracks identified during manufacturing quality checks could cause device failure.
Product
PRIMO MRI VR SureScan, Model Number DVMD3D4, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide

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6751–6775 of 39844