FoodJan 28, 2026
CATAO MARKET Gaceniga Authentic Cuban Loaf Cake Classic recall — FDA H-0412-2026
Undeclared colors FD&C Yellow #5
Class IIFDA: TerminatedCATAO MARKET LLC
Latest records
Latest recalls — page 113
The newest recall records with useful source details are listed here.
FoodJan 28, 2026
Lily's Bakery Factory Cuban Crackers Galletas Cubanas, Net Wt 8Oz recall — FDA H-0458-2026
Undeclared colors FD&C yellow #5, FD&C yellow #6, and FD&C red 40
Class IIFDA: TerminatedLily's Bakery Factory
FoodJan 28, 2026
GOLD STAR DISTRIBUTION All human food products distributed from the firm recall — FDA H-0411-2026
Potential exposure of rodents and rodent activity in the distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION INC
FoodJan 28, 2026
CATAO MARKET Mini Gaceniga Authentic Cuban Loaf Cake Classic recall — FDA H-0415-2026
Undeclared colors FD&C Yellow #5
Class IIFDA: TerminatedCATAO MARKET LLC
DrugJan 28, 2026
Zydus Pharmaceuticals (USA) Icosapent Ethyl capsules, 1 gram, 120-count bottles recall — FDA D-0295-2026
Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules
Class IIFDA: OngoingZydus Pharmaceuticals (USA) Inc
VehicleJan 27, 2026
Kia instrument cluster/panel recall — NHTSA campaign 26V046000
Kia America, Inc. (Kia) is recalling certain 2025 Kia K4, 2025-2026 Sorento, Sorento Hybrid, Sorento Plug-In Hybrid Electric (PHEV), 2026 Sportage, Sportage Hybrid, Sportage PHEV, K5, EV9,…
instrument cluster/panelKia America, Inc.
VehicleJan 27, 2026
Hyundai Motor instrument cluster/panel recall — NHTSA campaign 26V047000
Hyundai Motor America (Hyundai) is recalling certain 2025-2026 Tucson Hybrid, Tucson Plug-In Hybrid Electric (PHEV), 2026 IONIQ 5, Santa Cruz, Kona, Palisade, Palisade Hybrid, Santa Fe,…
instrument cluster/panelHyundai Motor America
VehicleJan 23, 2026
Palisade curtain recall — NHTSA campaign 26V034000
Hyundai Motor America (Hyundai) is recalling certain 2020-2025 Palisade vehicles. The side curtain air bags for third-row occupants may deploy improperly in a crash. As such, these vehicles…
curtainHyundai Motor America
VehicleJan 21, 2026
Explorer windshield recall — NHTSA campaign 26V024000
Ford Motor Company (Ford) is recalling certain 2026 Explorer vehicles. During manufacturing, the windshield may not have been properly bonded to the vehicle, allowing it to detach in a…
windshieldFord Motor Company
VehicleJan 21, 2026
Nissan latch recall — NHTSA campaign 26V023000
Nissan North America, Inc. (Nissan) is recalling certain 2025 Altima, Sentra, 2025-2026 Frontier, and 2026 Kicks vehicles. The door strikers may have been improperly welded and break,…
latchNissan North America, Inc.
Medical DeviceJan 21, 2026
Medline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M recall — FDA Z-1088-2026
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJan 21, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD20 recall — FDA Z-1066-2026
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceJan 21, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD10 recall — FDA Z-1073-2026
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceJan 21, 2026
Abbott Diabetes Care FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 recall — FDA Z-1023-2026
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Class IFDA: OngoingAbbott Diabetes Care, Inc.
Medical DeviceJan 21, 2026
PALACOS MV+G pro 40; PALACOS MV+G pro 80 recall — FDA Z-1082-2026
increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage.…
Class IIFDA: OngoingHeraeus Medical GmbH (Dental Division)
Medical DeviceJan 21, 2026
Medline Kits containing B recall — FDA Z-1050-2026
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJan 21, 2026
Abbott Diabetes Care FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 recall — FDA Z-1022-2026
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Class IFDA: OngoingAbbott Diabetes Care, Inc.
Medical DeviceJan 21, 2026
Medline Kits containing B recall — FDA Z-1052-2026
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJan 21, 2026
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING MAXXUS, System, Tomography, Computed, Emission recall — FDA Z-1047-2026
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product…
Class IIFDA: OngoingGE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
Medical DeviceJan 21, 2026
PALACOS R pro 40; PALACOS R pro 80 recall — FDA Z-1080-2026
increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage.…
Class IIFDA: OngoingHeraeus Medical GmbH (Dental Division)
Medical DeviceJan 21, 2026
Catalyst+ Catalyst, Catalyst+ recall — FDA Z-1092-2026
Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups. n certain cases, the system may indicate the patient…
Class IIFDA: OngoingC-RAD POSITIONING AB
Medical DeviceJan 21, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD20 Biplane recall — FDA Z-1071-2026
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceJan 21, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD20 OR Table recall — FDA Z-1072-2026
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceJan 21, 2026
Medline Kits containing B recall — FDA Z-1053-2026
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck…
Class IIFDA: OngoingMedline Industries, LP
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September 2026300 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