Medical DeviceJan 29, 2025
Adept Medical Otological Ventilation Tube - T-Tube 6mm - Double - Silicone recall — FDA Z-0964-2025
Lack of 510(k) clearance.
Class IIFDA: OngoingAdept Medical Ltd
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 148
Records are ordered by the best available source date.
Medical DeviceJan 29, 2025
CareFusion 303 BD Pyxis Med ES Auxiliary (AUX), REF 343 recall — FDA Z-0975-2025
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation…
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJan 29, 2025
Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument THUNDERBEAT 5 mm,35 cm recall — FDA Z-0996-2025
The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceJan 29, 2025
Percussionaire VDR4 Phasitron Breathing Circuit Models that contain the venturi component recall — FDA Z-0960-2025
Due to internal venturi component getting transiently stuck in the forward position within the breathing circuit and may cause a reduction of amplitude and volume of ventilation.
Class IFDA: OngoingPercussionaire Corporation
FoodJan 29, 2025
Braga Fresh Foods Marketside, BROCCOLI FLORETS, 12oz, BEST IF USED BY DEC 10 recall — FDA F-0424-2025
Potential contamination with Listeria monocytogenes.
Class IFDA: OngoingBraga Fresh Foods LLC
FoodJan 29, 2025
Acme Smoked Fish KIRKLAND Signature Smoked Salmon NET WT 340 g recall — FDA F-0420-2025
The firm was notified after laboratory analysis that the product test positive for Listeria monocytogenes.
Class IFDA: TerminatedAcme Smoked Fish Corp.
FoodJan 29, 2025
Lidl US TRADING Buttered Vegetables KEEP FROZEN NET WT 10.5 OZ recall — FDA F-0422-2025
Undeclared Milk. During an FDA investigation the manufacturer was notified that the label does not list the allergen milk in the ingredient statement.
Class IIFDA: TerminatedLidl US TRADING
FoodJan 29, 2025
Horizon Organic Aseptic Plain Whole Milk 8OZ 12 Pack recall — FDA F-0406-2025
Potential for premature product spoilage during shelf life.
Class IIFDA: TerminatedHorizon Organic Dairy, LLC
FoodJan 29, 2025
The Granola Bar brand The OG Bar recall — FDA F-0421-2025
Product contains undeclared milk and soy.
Class IIFDA: TerminatedThe Granola Bar
VehicleJan 29, 2025
Toyota Motor Engineering & Manufacturing column recall — NHTSA campaign 25V040000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2023 Toyota Corolla, Corolla Cross, Corolla Cross Hybrid, Highlander, Highlander Hybrid, Tacoma, Lexus RX350,…
columnToyota Motor Engineering & Manufacturing
DrugJan 29, 2025
SHOPPERS- PLAZA FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle, Sold and recall — FDA D-0207-2025
Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
Class IFDA: OngoingSHOPPERS- PLAZA
VehicleJan 23, 2025
Acura MDX back over prevention software recall — NHTSA campaign 25V032000
Honda (American Honda Motor Co.) is recalling certain 2025 Acura MDX vehicles. The touchscreen in the center console may go blank, resulting in the rearview camera image not displaying as…
back over prevention softwareHonda (American Honda Motor Co.)
VehicleJan 23, 2025
Forester wheels recall — NHTSA campaign 25V033000
Subaru of America, Inc. (Subaru) is recalling certain 2025 Forester vehicles equipped with 18" aluminum alloy wheels. The wheels may have been manufactured with an incorrectly specified lug…
wheelsSubaru of America, Inc.
VehicleJan 23, 2025
Honda fuel injection system recall — NHTSA campaign 25V031000
Honda (American Honda Motor Co.) is recalling certain 2022-2025 Acura MDX Type-S, 2023-2025 Honda Pilot, and 2021-2025 Acura TLX Type-S vehicles. A software error in the fuel injection…
fuel injection systemHonda (American Honda Motor Co.)
Medical DeviceJan 22, 2025
Cardinal Health Presource Kits: 1 ) TRIPLE ENDO PACK recall — FDA Z-0909-2025
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceJan 22, 2025
Intuitive Surgical 8MM,FENESTRATED BIPOLAR FORCEPS,IS4000 REF 471205 recall — FDA Z-0878-2025
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceJan 22, 2025
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING GE Healthcare Varicam Millennium VG Discovery recall — FDA Z-0900-2025
GE HealthCare has become aware that certain Infinia, VariCam/VG/VH, Brivo NM 615, Discovery NM 630, Discovery NM/CT 670, and Optima NM/CT 640 Nuclear Medicine systems (see Affected Products…
Class IIFDA: OngoingGE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
Medical DeviceJan 22, 2025
muRata Vios Monitoring System Model 2050 recall — FDA Z-0956-2025
During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms can become distorted and will flicker or flash very fast. This…
Class IIFDA: CompletedMurata Vios, Inc.
Medical DeviceJan 22, 2025
Intuitive Surgical 8MM,LONG BIPOLAR GRASPER,IS4000 REF 471400 recall — FDA Z-0882-2025
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceJan 22, 2025
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE recall — FDA Z-0837-2025
Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance.
Class IIFDA: OngoingKarl Storz Endoscopy
Medical DeviceJan 22, 2025
VITROS Chemistry Products DGXN Slides recall — FDA Z-0901-2025
Hemoglobin interference may occur at concentrations lower than the claimed 300 mg/dL, and may cause negatively biased digoxin results.
Class IIFDA: OngoingQUIDEL ORTHO
Medical DeviceJan 22, 2025
Intuitive Surgical 8MM,MEGA SUTURECUT ND,IS4000 REF 470309 recall — FDA Z-0865-2025
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceJan 22, 2025
Intuitive Surgical 8MM,TENACULUM FORCEPS,IS4000 REF 470207 recall — FDA Z-0860-2025
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceJan 22, 2025
Intuitive Surgical 8MM,CADIERE FORCEPS,IS4000 ¿ REF 470049 recall — FDA Z-0853-2025
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Class IIFDA: OngoingIntuitive Surgical, Inc.
About the 2025 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.