The Recall Desk

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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

2676–2700 of 30649

  • HighFDA (Devices)·Z-1095-2026·2026-01-21

    Coagulation Testing Device Recalled for Potential Microbial Contamination

    Instrumentation Laboratory is recalling approximately 7,720 coagulation testing devices due to potential microbial contamination. These devices are used to evaluate blood coagulation pathways and monitor heparin therapy.

    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-1053-2026·2026-01-21

    Medline IV Administration Sets Recalled for Stuck Check Valves

    Medline Industries is recalling 33 units of IV and pump administration sets due to check valve components that may become stuck in open or closed positions, potentially affecting fluid delivery.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: RR-LAP DONOR NEP ACCESSORY, Medline kit SKU DYNJ63395B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1099-2026·2026-01-21

    CentriMag blood pump may fail to lock securely to motor

    CentriMag blood pumps may fail to lock securely into their motors, potentially preventing proper alarm activation and causing delays in circulatory support or serious complications.

    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-1046-2026·2026-01-21

    GE HealthCare Nuclear Medicine Systems May Have Detector Mounting Failure

    Certain GE HealthCare nuclear medicine systems transported without proper detector support may have compromised mounting mechanisms, potentially resulting in detector fall and life-threatening injury. No injuries have been reported.

    Product
    SMV BodyTrack, System, Tomography, Computed, Emission
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1080-2026·2026-01-21

    Bone Cement Ampoules May Break or Fail to Break Properly

    Heraeus Medical is recalling PALACOS R pro bone cement due to ampoule breakage within the device system. If ampoules don't break properly, appropriate cement cannot be formed for use.

    Product
    Brand Name: PALACOS Product Name: PALACOS R pro 40; PALACOS R pro 80 Model/Catalog Number: 5081286; 5081287 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable fo
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1072-2026·2026-01-21

    Allura Xper FD20 operating room table cooling unit drip tray not installed

    Some Allura Xper FD20 operating room tables may lack a cooling unit drip tray, which could allow coolant to contact electrical components and cause system shutdown.

    Product
    Allura Xper FD20 OR Table; Model Number: 722023;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1092-2026·2026-01-21

    Patient positioning system software may fail to detect stereotactic radiosurgery positioning errors

    C-RAD Catalyst and Catalyst+ patient positioning systems for stereotactic radiosurgery may incorrectly indicate proper patient positioning, potentially compromising radiation treatment accuracy. Approximately 189 units have been distributed in 37 countries including the United States.

    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-1047-2026·2026-01-21

    GE MAXXUS Nuclear Medicine System Detector Mounting Mechanism Recall

    GE HealthCare is recalling certain MAXXUS nuclear medicine systems that may have been transported without proper detector support, potentially compromising mounting mechanisms. No injuries have been reported to date.

    Product
    MAXXUS, System, Tomography, Computed, Emission
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1042-2026·2026-01-21

    Boston Scientific Coyote Balloon Dilation Catheter Inflation Deflation Failure

    Boston Scientific is recalling certain batches of Coyote Over-the-Wire Balloon Dilation Catheters that may not properly inflate or deflate during use in peripheral vessels.

    Product
    Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter, 4F, 1) 2.5mm x120mm, 150 cm, UPM/Model No. REF H74939186251210; 2) 3.5mm x120mm, 150 cm, UPM/Model No. REF H74939186351210; Catheter, Angioplasty, Peripheral, Transluminal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1066-2026·2026-01-21

    Philips medical imaging system may lack cooling unit drip tray

    The Philips Allura Xper FD20 fluoroscopy system may lack a drip tray beneath its cooling unit, potentially allowing coolant to contact electrical components and cause device shutdown. The recall affects 143 units worldwide.

    Product
    Allura Xper FD20; Model Number: 722006;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1073-2026·2026-01-21

    Philips Allura Xper FD10 medical imaging system drip tray installation issue

    Philips is recalling the Allura Xper FD10 because the drip tray beneath the cooling unit may not be installed in some units, potentially allowing coolant to contact electrical components and cause system shutdown.

    Product
    Allura Xper FD10; Model Number: 722026;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1101-2026·2026-01-21

    Portex Spinal Tray syringes recalled due to syringe collar cracks

    ICU Medical is recalling Portex Spinal Tray syringes due to cracks in the syringe collar. The defect may cause delayed blood draws, fluid leakage during arterial blood sampling, or improper delivery.

    Product
    Portex Spinal Tray, Item No. A3729-24 A3595
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1068-2026·2026-01-21

    Philips Allura Xper FD10 imaging system recall for missing cooling unit drip tray

    Philips is recalling Allura Xper FD10 X-ray systems with potentially missing drip trays beneath the cooling unit. If missing, coolant could contact electrical components, causing short-circuits and system shutdown.

    Product
    Allura Xper FD10; Model Number: 722010;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1038-2026·2026-01-21

    Medicrea IB3D Universal Implant Inserter Handle May Separate During Surgery

    Medicrea is recalling 44 units of the IB3D Universal Implant Inserter due to a mechanical defect where the handle may separate from the shaft, preventing proper implant rotation during surgery.

    Product
    Medicrea, IB3D Universal Implant Inserter, Rx Only REF: A24000000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1060-2026·2026-01-21

    Medline IV Administration Kits Recalled for Stuck Check Valve Components

    Medline is recalling IV administration kits containing B. Braun components because check valves may become stuck in the open or closed positions. The recall affects 338 units distributed nationwide.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-PLASTIC CRANIOFACIAL PK-LF, Medline kit SKU DYNJ0395085V; 2) NH PERI DISC PACK, Medline kit SKU DYNJ66311C; 3) DISCECTOMY PACK, Medline kit SKU DYNJ86770; 4) TOTAL KNEE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1067-2026·2026-01-21

    Philips Allura Xper Biplane Systems Missing Critical Cooling Drip Tray

    Philips recalls Allura Xper FD20 Biplane systems with a missing cooling drip tray. Coolant exposure to electrical components could cause short-circuits and system shutdown.

    Product
    Allura Xper FD20 Biplane; Model Number: 722008;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1083-2026·2026-01-21

    Bone Cement Ampoule Breakage Defect Prompts Heraeus PALACOS Recall

    Heraeus Medical recalls PALACOS MV pro bone cement products due to ampoule breakage defects that prevent proper mixing. Affected devices may fail to produce usable cement during surgical application.

    Product
    Brand Name: PALACOS Product Name: PALACOS MV pro 40; PALACOS MV pro 80 Model/Catalog Number: 5150633; 5150635 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1094-2026·2026-01-21

    Plum Duo Infusion Pump speaker defects may silence alarms

    ICU Medical recalls Plum Duo Infusion Systems with defective speakers that may fail to produce sound. If the speaker fails, patients and caregivers may not hear pump alarms or alerts.

    Product
    Plum Duo Infusion System, List Number 40002-04-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1098-2026·2026-01-21

    Medtronic Abre Venous Stents recalled due to stent migration risk

    Medtronic is recalling certain Abre Venous Self-Expanding Stent Systems due to a manufacturing defect that can reduce stent diameter and radial force when deployed, potentially causing the stent to migrate.

    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-1085-2026·2026-01-21

    Medline medical robotics kits recalled for irrigation solution leakage during use

    Medline is recalling medical procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators due to a 2024 design change that allows irrigation solution to leak into the handpiece and battery pack during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS, REF DYNJ908777B; 2) CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1087-2026·2026-01-21

    Medline Surgical Kits with Strykeflow 2 Suction Irrigators Recalled for Leakage

    Medline surgical procedure kits containing Stryker Strykeflow 2 Suction Irrigators are recalled because a 2024 design change allows irrigation solution to leak into the handpiece and battery pack, potentially causing leakage or vaporized saline emission during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS, REF CDS860237AF; 2) ROBOTIC PROCEDURE, REF CDS982128Q; 3) CUH THORACIC, REF CDS984338M; 4) THORACIC PROCEDURE, REF CDS984640I; 5) DAVINCI ROBOTIC PACK-LF, REF DYNJ0525321O; 6) LAP CHO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1044-2026·2026-01-21

    Nuclear Medicine System Detector Mounting Structural Defect Recall

    GE HealthCare recalls nuclear medicine systems that may have structural damage to detector mounting mechanisms due to improper transport. Damaged detectors could fall and cause serious injury, though no incidents have been reported.

    Product
    SMV DSX New Line, System, Tomography, Computed, Emission
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1056-2026·2026-01-21

    Medline IV Administration Kits Recalled for Stuck Check Valve Defect

    Medline recalls IV administration kits because check valve components may become stuck, potentially affecting medication delivery. The recall affects 5,314 units distributed nationwide.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1071-2026·2026-01-21

    Philips Allura Xper FD20 biplane coolant leak risk from undocumented drip tray

    Philips has identified that some Allura Xper FD20 biplane systems may have uninstalled or undocumented drip trays beneath the cooling unit, creating risk for coolant to contact electrical components and cause system shutdown.

    Product
    Allura Xper FD20 Biplane; Model Number: 722013;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1050-2026·2026-01-21

    Medline Cardiac Procedure Kits Recalled Due to Stuck Check Valve in IV Administration Sets

    Medline has recalled 633 kits containing B. Braun IV Administration Sets and Pump Administration Sets due to customer complaints that check valve components may become stuck in open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) OPEN HEART ACCESSORY CDSKit SKU CDS984289O; 2) OPEN HEART CDSKit SKU CDS984355K; 3) BAG A OPEN HEART KITKit SKU DYKM1025D; 4) RR-CABG SUPPLEMENTAL PACKKit SKU DYNJ0394752
    Category
    Medical Device
    Distribution
    Distributed nationwide