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.

Agency

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

376–400 of 26077

SevereFDA (Devices)·Z-2231-2026·2026-06-03
Medline Anesthesia Kits Recalled for Quality and Efficacy Concerns
Medline is recalling 1100 anesthesia trays containing Bupivacaine due to quality issues, microbiology testing data integrity concerns, and reported efficacy complaints. The kits were distributed worldwide to healthcare facilities.
Product
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) ANESTHESIA TRAY, Medline SKU DYNJRA1355A; 2) SPINAL ANESTHESIA TRAY, Medline SKU DYNJRA2151.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2232-2026·2026-06-03
Medline Spinal Block Kits Recalled for Data Integrity and Efficacy Issues
Medline Industries recalled approximately 28,106 anesthesia kits containing Huons bupivacaine due to microbiology testing data integrity concerns and reported efficacy complaints.
Product
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) PAIN TRAY, Medline Kit SKU DYNJRA1555; 2) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1817; 3) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA1920; 4) ULTRASOUND
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2160-2026·2026-06-03
RelayPro Thoracic Stent-Graft System Proximal Clasp Disconnection
Bolton Medical's RelayPro Thoracic Stent-Graft System may fail to release from its delivery system due to proximal clasp disconnection. This FDA Class I recall affects multiple device configurations distributed worldwide.
Product
RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-32U 28-N4-32-209-28U 28-N4-32-209-32U 28-N4-32-259-32U 28-N4-34-109-34U 28-N4-34-154-30U 28-N4-34-154-34U 28-N4-34-209-30U 28-N4-34-209-34U 28-N4-34-259-34U 28-
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·H-0858-2026·2026-06-03
Wawa Fruit Punch Pint Recalled for Undeclared Milk Allergen
Wawa Beverage Company is recalling Wawa Fruit Punch Pint (16oz) bottles due to undeclared milk allergen. The product was distributed to Delaware, Maryland, New Jersey, Pennsylvania, and Virginia.
Product
Wawa Fruit Punch Pint (16oz), Plastic bottle
Category
Food
Distribution
5 states
SevereFDA (Food)·H-0852-2026·2026-06-03
Giant Eagle Baked Pita Chips Recalled for Salmonella Contamination
Giant Eagle Baked Pita Chips with Parmesan, Garlic & Herb and Bagel Crisps are recalled due to Salmonella contamination from California Dairies milk powder. The affected products were distributed in Pennsylvania and Wisconsin.
Product
giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt 7.33 oz. Shipping Case: 12 ct - 7.33 oz Bags Net Weight: 5.49 lbs. Legacy Bakehouse, LLC, Waukesha WI 53186.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-2260-2026·2026-06-03
Medline Medical Convenience Kit Recalled: Wrong Syringe Type Inside
Medline medical convenience kits are being recalled because the outer carton is mislabeled. The packaging states the contents are 1 mL Luer Lock Tuberculin Syringes, but the actual syringes inside are U-100 insulin syringes.
Product
Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2230-2026·2026-06-03
Halyard Purezero Ultraviolet Nitrile Exam Gloves Recalled for Chemical Permeation Failure
O&M Halyard is recalling approximately 452,500 Purezero Ultraviolet Nitrile Exam Gloves due to failure to meet chemical permeation performance specifications, potentially exposing users to chemical penetration.
Product
Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2243-2026·2026-06-03
GE APEXPRO and CARESCAPE Telemetry Systems Risk Loss of Patient Monitoring
GE Medical Systems is recalling APEXPRO v5.0 and v6.0 telemetry monitoring systems due to potential loss of ECG and SpO2 monitoring during network connectivity issues. The recall affects 14 units distributed worldwide.
Product
GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2245-2026·2026-06-03
Patient Telemetry Server Potential Loss of ECG and SpO2 Monitoring Function
GE HealthCare CARESCAPE Telemetry Server (ARK-2250L) may lose ECG and SpO2 monitoring capability during network communication failures. Approximately 1,249 units have been recalled worldwide.
Product
GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Category
Medical Device
Distribution
0 states
HighFDA (Food)·H-0854-2026·2026-06-03
Fly By Jing Creamy Sesame Noodles recalled for possible undeclared peanut allergen
Fly By Jing Inc. is recalling Creamy Sesame Noodles due to possible cross-contamination with undeclared peanut. Consumers with peanut allergies should not consume affected products.
Product
Fly By Jing (branded) Creamy Sesame Noodles; 3.8 oz packets. Sold in single and 4 packs. Single UPC: 8-50052-23988-6 4 pack UPC: 8-50052-23991-6
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2258-2026·2026-06-03
Philips Azurion and Allura Imaging Systems Recalled for Hard Drive Degradation
Philips is recalling certain Azurion and Allura medical imaging systems due to potential hard drive degradation after six years of service. The issue may cause loss of imaging functionality or motorized movement, though no injuries have been reported.
Product
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2259-2026·2026-06-03
Philips Allura Imaging Systems Hard Drive Degradation Affects Functionality
Philips Allura fluoroscopic imaging systems may experience hard drive degradation after six years of service, potentially resulting in loss of imaging capability and motorized movement.
Product
Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allur
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2242-2026·2026-06-03
GE CARESCAPE Telemetry Server may lose patient ECG and oxygen saturation monitoring
GE HealthCare is recalling CARESCAPE Telemetry Server v5 (476 units) because network failures can cause loss of ECG and SpO2 monitoring at the central station. Affected systems are used in healthcare facilities worldwide.
Product
GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2244-2026·2026-06-03
GE HealthCare CARESCAPE Telemetry Server May Lose Cardiac Monitoring
GE HealthCare CARESCAPE Telemetry Servers (versions 5.0 and 6.0) may lose ECG and SpO2 patient monitoring during network connectivity failures. Seven affected units have been identified worldwide.
Product
GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2246-2026·2026-06-03
GE CARESCAPE Telemetry Server monitoring loss during network connectivity failures
GE HealthCare CARESCAPE Telemetry Server may lose ECG and SpO2 monitoring capability during persistent network connectivity failures at the Central Station, potentially delaying detection of patient changes.
Product
GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2247-2026·2026-06-03
GE HealthCare ApexPro Cardiac Monitor May Lose ECG and SpO2 Monitoring
GE HealthCare ApexPro v6.0 cardiac telemetry software may experience loss of cardiac and oxygen monitoring due to network disconnection at the central monitoring station. Approximately 2,187 units are affected worldwide.
Product
GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Category
Medical Device
Distribution
0 states
HighNHTSA·25V170000·2026-06-03
2025 Tesla Cybertruck Light Bar Can Delaminate and Detach
Tesla is recalling 2024-2025 Cybertruck vehicles because the light bar can delaminate and detach, potentially becoming a road hazard and increasing crash risk.
Product
TESLA — 2025 TESLA CYBERTRUCK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V135000·2026-06-03
2026 Kia K4 vehicles recalled for defective rear seat belt anchor
Kia is recalling certain 2026 K4 vehicles because the rear center seat belt anchor buckle may not latch properly, risking occupant restraint failure in a crash.
Product
KIA — 2026 KIA K4
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V102000·2026-06-02
2025 Volvo VNR trucks recalled for delayed brake activation defect
Volvo Trucks is recalling certain 2023-2025 VN trucks because their brakes may take longer than expected to activate, increasing the stopping distance and crash risk. Dealers will install a new pneumatic circuit.
Product
VOLVO — 2025 VOLVO VNR (4)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V068000·2026-06-02
2025-2026 Hyundai IONIQ 5 and 2026 IONIQ 9 Battery Fire Risk Recall
Hyundai is recalling certain 2025-2026 IONIQ 5 and 2026 IONIQ 9 vehicles due to an improperly tightened bus bar in the high voltage battery system that can cause an electrical short and increase fire risk.
Product
HYUNDAI — 2025 HYUNDAI IONIQ 5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V069000·2026-06-02
2026 Hyundai Kona vehicles recalled for front steering knuckle defect
Hyundai is recalling certain 2026 Kona vehicles because the front steering knuckles may crack and break due to a manufacturing error, which can cause loss of steering control and increase crash risk.
Product
HYUNDAI — 2026 HYUNDAI KONA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V073000·2026-06-02
Mercedes-Benz EQB high voltage battery fire hazard recall
Mercedes-Benz USA is recalling certain 2022-2024 EQB models due to a high voltage battery defect that may cause vehicle fires. Owners should park outside and limit charging to 80% until repairs are completed.
Product
MERCEDES-BENZ — 2022 MERCEDES-BENZ EQB 300 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V070000·2026-06-02
Water Accumulation in Air Bag Control Units Affects Mercedes-Benz Metris
Water can accumulate on the air bag control unit in certain 2020-2023 Mercedes-Benz Metris right-hand-drive vehicles, preventing air bags from deploying in a crash.
Product
MERCEDES-BENZ — 2020 MERCEDES-BENZ METRIS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V052000·2026-06-01
Spartan K Series RV Chassis Steering Gear Defect May Cause Power Loss
Shyft Group is recalling approximately 797 Spartan K2, K3, and K4 RV chassis from 2023-2025 due to foreign material in the steering gear that may cause loss of power steering assist, increasing crash risk.
Product
SPARTAN — 2023 SPARTAN K2
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V053000·2026-06-01
2024 Nissan Murano Recalled for Detaching Quarter Glass Panels
Nissan is recalling certain 2024 Murano vehicles due to defective primer on quarter glass panels, which may cause them to detach. Detached glass becomes a road hazard and increases crash risk.
Product
NISSAN — 2024 NISSAN MURANO
Category
Vehicle
Distribution
Distributed nationwide

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