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.

376–400 of 50462

  • HighFDA (Devices)·Z-2986-2026·2026-08-26

    ConvaTec Esteem Body Soft Convex Urostomy Pouches Recalled for Leakage

    ConvaTec is recalling Esteem Body Soft Convex Urostomy Pouches because they may leak from the cap during use.

    Product
    Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703, 423704, 423705, 423707, 423708, 423709, 423710, 423712, 423713, 423714, 423715, 423716, 423717, 423718, 423721, 423722, 423723, 423725, 423726, 423727.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V549000·2026-08-25

    Mitsubishi Recalls Outlander Models for Rearview Camera Software Defect

    Mitsubishi is recalling 2025-2026 Outlander and 2026 Outlander PHEV vehicles because a software error may prevent the rearview camera image from displaying, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V541000·2026-08-21

    Altec Recalls Aerial Devices and Digger Derricks Due to Braking Calibration Issue

    Altec is recalling specific aerial devices and digger derricks because the automatic braking system was not recalibrated after moving the front radar box, increasing crash risk.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AM SERIES AERIAL DEVICE, AA SERIES AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V539000·2026-08-20

    GM Recalls Buick and Chevrolet SUVs for Rearview Camera Defect

    General Motors is recalling 2024-2026 Buick and Chevrolet SUVs because the rearview camera may display a distorted or blank image, increasing crash risk.

    Product
    BUICK — BUICK, CHEVROLET ENCORE GX, ENVISTA, TRAILBLAZER, TRAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26714·2026-08-20

    Koorlian Mattresses Recalled for Fire Hazard Violating Flammability Standards

    CPSC recalls Koorlian mattresses sold on Amazon due to fire risks from violating mandatory flammability standards. Consumers should stop using them and contact the manufacturer for a free cover.

    Product
    Koorlian Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26716·2026-08-20

    CCM Hockey Recalls FMHVR Visors and ACCHVR Accessories Due to Laceration Risk

    CCM Hockey is recalling FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories because they can crack upon impact, posing a risk of laceration or impact injury.

    Product
    FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26C006000·2026-08-20

    Britax Recalls Infant Car Seats Due to Handle Detachment Risk

    Britax is recalling specific infant car seats because a screw in the carrying handle may come loose, causing the handle to partially detach and increasing the risk of a child falling.

    Product
    CHILD SEAT:HANDLE (INFANT) recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V568000·2026-08-20

    Ford F-650 SD Recall: Liftgate Platform Deck Pins May Break

    Marathon Industries is recalling one 2025 Ford F-650 SD because deck pins may break, causing the liftgate platform to fall and increasing injury risk.

    Product
    FORD — FORD F-650 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0751-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling specific lots of Semaglutide 9mg vials because they contain nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1224-2026·2026-08-19

    SHEANDRO Vodka Tomato Sauce Recalled for Undeclared Milk Allergen

    SHEANDRO LLC is recalling Vodka Tomato Sauce because the label declares cream and cheese but fails to declare milk, a major allergen.

    Product
    Vodka Tomato Sauce, NET WT. 24 oz / 680g, glass jar packed 12 jars in a carton.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2919-2026·2026-08-19

    V-Loc 180 Absorbable Wound Closure Device Recalled for Packaging Defects

    FDA is recalling V-Loc 180 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that could lead to biocontamination.

    Product
    V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY PASS FINAL BOX07405V1 BOX BYPASS CARDON BOX01056V2 BOX BYPASS DR LAGAE BOX01482V2 BOX BYPASS KIT DEZEMBER 2025 BOX09222V1 BOX BYPASS KIT NEU BOX 003…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2937-2026·2026-08-19

    Bioporto ProNephro AKI Reagent Kit Recalled for Non-Validated Rework Process

    Bioporto Diagnostics is recalling ProNephro AKI Reagent Kits because a non-validated rework process could lead to missed diagnoses of renal disease.

    Product
    ProNephro AKI (NGAL) Reagent Kit (100 tests). IVD Acute Kidney Injury Test System.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·26E059000·2026-08-19

    Avride Recalls Automated Driving Systems Due to Unsafe Lane Changes

    Avride Inc. is recalling Automated Driving Systems (ADS) with specific software versions that may cause unsafe lane changes or merging without yielding.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2941-2026·2026-08-19

    BD Medical Extension Sets Recalled for Potential Sterilization Defects

    BD Switzerland is recalling 93,700 intravascular extension sets because they may not have received adequate sterilization processing.

    Product
    60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 9 IN Extension Set w/Max Y REF MPX5300-C UDI-DI code: 10885403237218 Intravascular Administration Set and…
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-2918-2026·2026-08-19

    V-Loc 90 Absorbable Wound Closure Devices Recalled for Packaging Defects

    Covidien, LP is recalling V-Loc 90 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that may cause biocontamination.

    Product
    V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 GS-25 VLOCM0436 VLOCM0436 VLOCM0003 V-LOC* 90 4-0 CLR 15CM P12X12 VLOCM0003 VLOCM0013 V-LOC* 90 4-0 CLR 30CM P12X12 VLOCM0013 VLOCM0024 V-LOC* 90 3-0 CLR 45CM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2926-2026·2026-08-19

    Medline Micro-Kill Bleach Germicidal Wipes Recalled for Reduced Concentration

    Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because bleach concentration may drop below specification, potentially compromising disinfection effectiveness.

    Product
    Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2921-2026·2026-08-19

    Surgipro Sutures Recalled for Potential Sterile Barrier Perforation

    FDA is recalling Surgipro sutures due to potential sterile barrier defects that could cause biocontamination and infection.

    Product
    Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2949-2026·2026-08-19

    Cardinal Health Presource Kits Recalled for Endotoxin Variability

    Cardinal Health is recalling 616 Presource Kits because they contain sponges with unexpected endotoxin variability.

    Product
    Cardinal Health Presource Kits: 1) BASIC PACK , Catalog Number: SBA73BPGCA; 2) SPINE PACK , Catalog Number: SNE11SPHKC; 3) SPINE PACK , Catalog Number: SNE11SPHKD; 4) CRANIOTOMY PACK , Catalog Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2934-2026·2026-08-19

    Waldemar Link Recalls Endo-Model Tibial Plateau Replacement Sets

    Waldemar Link is recalling Endo-Model tibial plateau replacement sets that incorrectly contain a Pure Hinge plateau, posing a risk of increased wear if implanted.

    Product
    Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2948-2026·2026-08-19

    Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges

    Cardinal Health 200, LLC is recalling 52,699 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.

    Product
    Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH4; 3) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH5; 4) KIT, ANT CERVICAL DISC , Catalog Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2912-2026·2026-08-19

    Microvention Recalls Bobby Balloon Guide Catheters Due to Pinhole Defects

    Microvention Inc. is recalling 5,500 Bobby Balloon Guide Catheters worldwide due to an increased rate of balloon pinhole defects.

    Product
    BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an intravascular catheter into a selected blood vessel in the peripheral and neurovascular systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2924-2026·2026-08-19

    Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness

    Medline is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness, potentially allowing pathogenic microorganisms to survive.

    Product
    Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2928-2026·2026-08-19

    Philips Allura Xper FD Fluoroscopic X-Ray System Recalled for Firmware Issue

    Philips is recalling 4,252 Allura Xper FD interventional fluoroscopic x-ray systems worldwide due to a firmware issue that may cause loss of geometry movements.

    Product
    Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide