The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

601–625 of 52881

  • HighFDA (Devices)·Z-2514-2026·2026-06-24

    BD Connecta stopcock Port C may over thread rather than tightening

    BD Connecta BD Luer-Lok 360 stopcocks, REF 394910, are being recalled because the Port C connection may over thread or spin rather than tightening securely. 2,465,500 units affected.

    Product
    BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer fluids or medication through one or two different ports via an IV cannula or extension tube. The ports can be used to sample blood or for hemodynamic monitoring.
    Category
    Medical Device
    Distribution
    39 states
  • HighFDA (Devices)·Z-2495-2026·2026-06-24

    Medline urethroplasty kits contain catheters failing performance specifications

    Medline urology urethroplasty procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 91 units are affected.

    Product
    MEDLINE Medical Procedure Kits labeled as: 1) KIT UROLOGY URETHROPLASTY, Medline Kit Number/SKU DYKMBNDL117C; 2) URETHROPLASTY, Medline Kit Number/SKU DYNJ908978; 3) URETHROPLASTY, Medline Kit Number/SKU DYNJ908978F.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2489-2026·2026-06-24

    Medline vasectomy reversal kits contain catheters failing performance specifications

    Medline Bilateral Micro Vasectomy Reversal kits are being recalled because representative samples did not meet applicable catheter performance specifications. 588 units affected.

    Product
    MEDLINE Medical Procedure Kits labeled as: BILAT MICRO VASECTOMY REVERSAL, Medline Kit Number/SKU DYNJ68302
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2499-2026·2026-06-24

    Medline nursing kits contain catheters failing applicable performance specifications

    Medline Nursing Kits, SKU EDUC1044, are being recalled because representative samples did not meet applicable catheter performance specifications. 730 units are affected.

    Product
    MEDLINE Medical Procedure Kits labeled as: NURSING KIT, Medline Kit Number/SKU EDUC1044
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2486-2026·2026-06-24

    Medline cardiac surgery and ECMO packs contain substandard catheters

    Medline cardiac procedure kits including basic heart, cardiac surgery, carotid endarterectomy and ECMO packs are being recalled over catheter specification failures. 4,801 units affected.

    Product
    MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK, Medline Kit/SKU DYNJ67331B; 2) CARDIAC SURGERY, Medline Kit/SKU DYNJ911589A; 3) CAROTID ENDARTECOMY, Medline Kit/SKU DYNJ36211D; 4) CHLA ECMO / CARDIAC PACK, Medline Kit/SKU DYNJ87973; 5) CHLA ECMO / CARDI
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26E038000·2026-06-23

    Ricon Recalls S-Series and K-Series Wheelchair Platform Lifts

    Ricon is recalling S-Series and K-Series wheelchair platform lifts because a failed electrical contactor may prevent the controls from stopping the lift.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY:WHEELCHAIR LIFT/RAMP:CONTROLS/CONTROL WIRING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E037000·2026-06-23

    Rockford Fosgate Amplifier Kits Recalled for Fire Risk

    Rockford Corporation is recalling specific amplifier kits because a fuse may fail to protect against short circuits, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:WIRING:FUSES AND CIRCUIT BREAKERS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V400000·2026-06-23

    Hyundai Tucson instrument panel displays may fail due to software error

    Hyundai is recalling certain 2025-2026 Tucson, Tucson Hybrid and Tucson Plug-In Hybrid vehicles because a software error may cause the instrument panel display to fail.

    Product
    HYUNDAI — HYUNDAI TUCSON, TUCSON HYBRID, TUCSON PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V397000·2026-06-19

    Indian Motorcycle Recalls 2026 Chief Vintage for Incorrect Rim Labeling

    Indian Motorcycle is recalling 2026 Chief Vintage models because the VIN label lists the wrong rear rim width, which could lead to improper tire mounting and loss of control.

    Product
    INDIAN — INDIAN CHIEF VINTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26568·2026-06-18

    Joolz Aer2 car seat adapters can detach, allowing the seat to fall

    About 3,840 Joolz Aer2 Car Seat Adapters are being recalled because they can fail to attach properly to the stroller, which may allow the car seat to fall.

    Product
    Joolz Aer2 Car Seat Adapters for Joolz Aer 2 Stroller
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V393000·2026-06-18

    2026 Subaru Solterra battery electric vehicles loss of drive power

    Toyota Motor Engineering & Manufacturing is recalling 2026 Subaru Solterra vehicles due to a fault in the battery electronic control unit that may cause loss of drive power, increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA, SUBARU RZ, BZ, SOLTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26564·2026-06-18

    Veseacky Children's Pajama Sets Recalled for Burn Hazard

    Veseacky children's pajama sets are recalled due to burn hazards from violating mandatory safety standards for children's sleepwear. About 3,700 units were sold on Amazon from October 2020 through January 2026.

    Product
    Veseacky Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26567·2026-06-18

    Children's Pajamas Recalled by SHEIN Over Burn Hazard

    SHEIN Distribution Corporation is recalling about 160 Michley children's pajamas that violate the mandatory flammability standard for children's sleepwear, posing a burn injury or death risk. No injuries have been reported.

    Product
    Michley Children's Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26561·2026-06-18

    BABESIDE doll and stroller toy sets violate the small parts ban

    About 2,200 BABESIDE doll and stroller toy sets are being recalled because the small pacifier violates the small parts ban and the plush bear's eyes can detach.

    Product
    BABESIDE Doll and Stroller Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V394000·2026-06-18

    2026–2027 Cadillac Vistiq Third-Row Seat Power Fold Feature Recall

    General Motors is recalling 2026–2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse when it encounters a person, potentially trapping them.

    Product
    CADILLAC — CADILLAC VISTIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26565·2026-06-18

    Arizer Solo III vaporizers recalled after four battery explosion reports

    About 5,000 Arizer Solo III Intergalactic (Black) portable vaporizers are being recalled after four reports of the internal lithium-ion battery exploding or igniting.

    Product
    Arizer Solo III portable electronic vaporizers (Intergalactic/Black color only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V395000·2026-06-18

    Farber Specialty Recalls 2025-2026 Emergency Vehicles Due to Touchscreen Failure

    Farber Specialty is recalling 2025-2026 HX620 and MCXCR emergency vehicles because the touchscreen may fail, preventing the activation of exterior lights and emergency equipment.

    Product
    FARBER SPECIALTY — FARBER SPECIALTY HX620 SBA 6X4, MCXCR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2324-2026·2026-06-17

    TDC VELOCE 27 gauge vitrectomy cutters may have loose outer knife

    TDC VELOCE 27G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.

    Product
    TDC VELOCE", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01, 9311.27K02, 9311.27K03, 9627.G0101, 9627.G0201, 9311.27G01-00;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2322-2026·2026-06-17

    TDC VELOCE 23 gauge vitrectomy cutters may have loose outer knife

    TDC VELOCE 23G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.

    Product
    TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2352-2026·2026-06-17

    MIC Safety 24 Fr pull ENFit PEG kits contain recalled lidocaine

    MIC Safety PEG Kits with ENFit Connectors, 24 Fr PULL, catalog number 8180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2398-2026·2026-06-17

    Siemens Dimension tacrolimus reagent cartridges may bias results positively

    Three lots of the Siemens Dimension Tacrolimus Flex reagent cartridge are being recalled because of a potential positive bias in quality control and patient sample results.

    Product
    Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay
    Category
    Medical Device
    Distribution
    Distributed nationwide