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

1976–2000 of 39987

ModerateFDA (Devices)·Z-1132-2026·2026-01-28
Long distal radius plates recalled over an incorrect thread orientation
Tyber Medical is recalling 64 units VOLT Wrist Treatment System distal radius plates because the supplier manufactured anatomical left plates with an incorrect thread orientation.
Product
Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/14Shaft/Left/Std/186mm Model/Catalog Number: 02.426.691S Product Description: 2 Column Distal Radius Plate - 6 Head, 14 Shaft, Standard Left - 186mm Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1137-2026·2026-01-28
TRAM powered lift devices recalled over potential strap fraying
Community Products is recalling 3,238 units of the Rifton TRAM over potential fraying on the body support strap.
Product
Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1139-2026·2026-01-28
Gait training devices recalled over potential fraying on the body support strap
Community Products is recalling 470 units of the Rifton E-Pacer gait training device over potential fraying on the body support strap.
Product
Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1133-2026·2026-01-28
Reusable hip trial components recalled over missing FDA premarket authorization
MicroPort Orthopedics is recalling 91 units of the HIPTURN 36mm reusable femoral head trial because the product does not have FDA premarket authorization for US distribution.
Product
Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software Version: N/A Product Description: HIPTURN FEM HEAD TRIAL 36MM REUSABLE
Category
Medical Device
Distribution
13 states
ModerateFDA (Food)·H-0414-2026·2026-01-28
Infusion pumps recalled over hard limit messages blocking piggyback flush programming
ICU Medical is recalling Plum Duo Precision IV Pumps because clinicians may receive an Upper or Lower Hard Limit violation message that prevents a piggyback flush from being programmed.
Product
Mini Gaceniga Authentic Cuban Loaf Cake Raisins (Net Wt. 12 oz (340g)) packaged in wax paper, placed in clear bag and packed in cardboard carton. 12/ 12 oz per master case.
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1120-2026·2026-01-28
Plum Solo pumps recalled over hard limit messages blocking flush programming
ICU Medical is recalling the Plum Solo Precision IV Pump because clinicians may receive an Upper or Lower Hard Limit violation message that prevents a piggyback flush from being programmed.
Product
ICU Medical Plum Solo Precision IV Pump, List Numbers: 400010401 (US), 400011001 (Philippines)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1155-2026·2026-01-28
Telemetry transmitters recalled over potential cybersecurity issues flagged by FDA
Edan Diagnostics is recalling 1,457 units of its iT20 Telemetry Transmitter after an FDA letter raising potential cybersecurity issues with the firm's devices.
Product
Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number: iT20 Product Description: iT20 collects physiological parameters by ECG cables and SpO2 sensors, then achieves data analyzing and processing. After that, data will be sent to MFM-CMS via Wi-Fi. The para
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1130-2026·2026-01-28
Surgical laser consoles recalled over a label missing the DANGER symbol
Leaseir Technologies is recalling two MHR Xcell surgical laser systems because the console label on the affected devices is missing the "DANGER" symbol.
Product
Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b Software Version: 1.5.0.0 Product Description: The Leaseir MHR Xcell is a surgical laser instrument for use in general and plastic surgery and dermatology, intended for hair removal and treatm
Category
Medical Device
Distribution
Distributed nationwide
CriticalCPSC·26215·2026-01-22
Semi electric homecare beds recalled over hand pendants that may overheat
Medline is recalling 373,392 units of the Semi Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Product
Mikario Trading 5-in-1 Convertible Baby Gyms
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1021-2026·2026-01-21
Libre 3 Plus sensors recalled in a second lot over carbon build up
Abbott Diabetes Care is recalling 1,663,241 FreeStyle Libre 3 Plus sensors, REF 78768-01, because carbon build up in the sensor may result in incorrect low glucose results.
Product
FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Category
Medical Device
Distribution
36 states
CriticalFDA (Devices)·Z-1020-2026·2026-01-21
Glucose monitoring sensors recalled over carbon build up causing low readings
Abbott Diabetes Care is recalling 1,060,723 FreeStyle Libre 3 sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.
Product
FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Category
Medical Device
Distribution
36 states
CriticalFDA (Devices)·Z-1022-2026·2026-01-21
Libre 3 Plus sensors, REF 78769-01, recalled over carbon build up
Abbott Diabetes Care is recalling 258,913 FreeStyle Libre 3 Plus sensors, REF 78769-01, because carbon build up in the sensor may result in incorrect low glucose results.
Product
FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Category
Medical Device
Distribution
36 states
CriticalFDA (Devices)·Z-1023-2026·2026-01-21
Libre 3 Plus sensors recalled over carbon build up causing low readings
Abbott Diabetes Care is recalling 8,062 FreeStyle Libre 3 Plus sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.
Product
FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Category
Medical Device
Distribution
36 states
HighFDA (Devices)·Z-1071-2026·2026-01-21
MRI systems recalled over ice that may block the magnet venting system
Canon Medical Systems is recalling 34 Vantage Galan 3T MRI systems because ice may form in the venting system, and a quench in that condition could rupture the helium vessel.
Product
Allura Xper FD20 Biplane; Model Number: 722013;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1044-2026·2026-01-21
SMV DSX New Line systems recalled over a potential detector fall
GE HealthCare is recalling 7 units of the SMV DSX New Line nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.
Product
SMV DSX New Line, System, Tomography, Computed, Emission
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1098-2026·2026-01-21
Venous stents recalled over a nitinol anomaly that reduces deployed diameter
Medtronic is recalling 442 Abre Venous Self-Expanding Stent Systems because a nitinol anomaly causes a reduced stent diameter and radial force when deployed, which may result in migration.
Product
Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G12100090 AB9G14080090 AB9G12080090 AB9U12060090 AB9U14100090 AB9U14080090 AB9U12080090 AB9U14060090 AB9G14100090 AB9G12060090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1096-2026·2026-01-21
Surgical access port kits recalled over trays that may crack
Intuitive Surgical is recalling 41,526 da Vinci SP Access Port Kits because the Access Port System tray may develop cracks, potentially resulting in a sterility breach.
Product
da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075 (2.7-7cm,SP1098,Box)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0401-2026·2026-01-21
SMV BodyTrack nuclear medicine systems recalled over a potential detector fall
GE HealthCare is recalling 12 units of the SMV BodyTrack nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.
Product
Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. 32 OZ (2 LB) 907g UPC: 1 93968 00697 6
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1092-2026·2026-01-21
Patient positioning systems recalled over stereotactic radiosurgery tolerance errors
C-RAD Positioning is recalling 189 Catalyst and Catalyst+ systems because the system may indicate a patient as correctly positioned at the isocenter when it is outside tolerance.
Product
Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version: cSRS module in combination with cMotion module Product Description: GMDN: 40893 Patient positioning device, diagnostic imaging/radiotherapy, laser Component
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1078-2026·2026-01-21
Oncology information system recalled over a potential for overtreatment
Elekta is recalling a MOSAIQ Oncology Information System with Particle Therapy License because a specific sequence can result in a partial treatment being delivered twice.
Product
MOSAIQ Oncology Information System with Particle Therapy License (License Kit 45700000000IQRO)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1095-2026·2026-01-21
Coagulation reagent recalled over potential for microbial contamination
Instrumentation Laboratory is recalling 7,720 units of a coagulation reagent used for evaluating the intrinsic pathway and monitoring heparin therapy over potential microbial contamination.
Product
The product is used for the evaluation of the intrinsic coagulation pathway, APTT substitution test and the monitoring of heparin therapy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1099-2026·2026-01-21
Circulatory support blood pumps recalled over locking into the motor
Thoratec is recalling 8,399 CentriMag blood pump products after reports that the pump may not fit or lock securely into the motor using the screw-in locking feature.
Product
CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag Pre-connected Pack, REF: CMAEK00; CentriMag VAD KIT, REF: 201-51006, 201-51007, 201-90001 201-90001T; Blood Pump with CentriMag Acute Circulatory Support System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1045-2026·2026-01-21
SMV DSI nuclear medicine systems recalled over a potential detector fall
GE HealthCare is recalling 3 units of the SMV DSI nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.
Product
SMV DSI, System, Tomography, Computed, Emission
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1018-2026·2026-01-21
MRI systems recalled over ice that may block magnet venting
Canon Medical Systems is recalling 22 Vantage Titan 3T MRI systems because ice in the magnet venting system could lead to a helium vessel rupture during a quench.
Product
VANTAGE TITAN 3T Model MRT-3010/MEXL-3010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1101-2026·2026-01-21
Spinal tray syringes recalled over a crack on the syringe collar
ICU Medical is recalling 64,290 Portex Spinal Trays because syringes may have a crack on the collar, which may lead to delayed or repeated blood draws and blood leakage.
Product
Portex Spinal Tray, Item No. A3729-24 A3595
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

1976–2000 of 39987