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.

851–875 of 21614

  • HighFDA (Devices)·Z-1951-2026·2026-05-06

    Philips Achieva 1.5T MRI Scanner Stiffness Calculation Error Recall

    Philips is recalling Achieva 1.5T MRI systems with MR Elastography software due to potential stiffness value errors that may occur with specific image reconstruction parameters, causing incorrect voxel size display in the default scan protocol.

    Product
    Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781196. 2. Model Number (REF): 781296.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2041-2026·2026-05-06

    Medline and Centurion Medical Convenience Kits Recalled for Non-Sterile Alcohol Prep Pads

    Medline Industries is recalling specific lots of medical convenience kits containing non-sterile Webcol Large Alcohol Prep Pads due to discovery of Paenibacillus phoenicis contamination. Affected kits were distributed nationwide.

    Product
    Medline and Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: 1. FOLEY CARE KIT, Medline Kit SKU UROT1044; 2. IV START KIT WITH EXTENSION TUBING, Medline Kit SKU IV8770; 3. IV START KIT, Medline Kit SKU DYNDV2520; 4. ARTERIAL LINE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1987-2026·2026-05-06

    DePuy Synthes ATTUNE Revision Hinge Femoral Component Sterility Recall

    DePuy Synthes is recalling one lot of ATTUNE Revision Hinge Femoral components (left size 7, part number 150450107) due to external sterile packaging adhered to internal packaging, potentially compromising product sterility.

    Product
    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2011-2026·2026-05-06

    Medline medical procedure kits recalled for out-of-specification endotoxin levels

    Medline Industries is recalling medical procedure kits containing Neuro Sponges for spinal fusion due to higher-than-expected endotoxin levels that may be out-of-specification.

    Product
    Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPINAL FUSION, Medline Kit Number/SKU CDS860017AG
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2017-2026·2026-05-06

    Medline Medical Procedure Kits with Neuro Sponges Recalled for Endotoxin

    Medline Industries is recalling multiple medical procedure kits containing Medline Neuro Sponges due to higher-than-expected endotoxin levels. The affected kits were distributed worldwide.

    Product
    Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. VP SHUNT, Medline Kit Number/SKU CDS840193V; 2. SHY VP SHUNT CDS, Medline Kit Number/SKU CDS982389J; 3. VP SHUNT ADULT PACK-LF, Medline Kit Number/SKU DYNJ0117497G; 4. PICC LINE PACK
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1999-2026·2026-05-06

    Abbott i-STAT EG7+ Blood Gas Cartridges Reporting Inaccurate Results

    Abbott Point Of Care is recalling approximately 7.6% of specific i-STAT EG7+ cartridge lots due to a manufacturing issue causing falsely high pCO2 and low pH readings. Inaccurate results could lead clinicians to make unnecessary or harmful medical interventions.

    Product
    i-STAT EG7+ cartridge; List Number: 03P76-25;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0678-2026·2026-05-06

    [pending] 52USA brand POPPING BOBA; MANGO FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose s

    Pending LLM rewrite. Source: FDA_FOOD H-0678-2026.

    Product
    52USA brand POPPING BOBA; MANGO FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic acid (E296), sodium alginate (E401), citric acid (E330), carrageenan (EE407), potas
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2018-2026·2026-05-06

    Medline medical procedure kits recalled for elevated endotoxin levels

    Medline Industries is recalling 208 medical procedure kits containing Neuro Sponges due to higher-than-expected endotoxin levels that may exceed product specifications.

    Product
    Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. OSC COLEMAN FAT HARVEST KIT, Medline Kit Number/SKU DYNJ32854B; 2. RR-DR. CHHETRI MDL PACK, Medline Kit Number/SKU DYNJ62635B.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·26V283000·2026-05-05

    [pending] 2021 TESLA MODEL Y

    Pending LLM rewrite. Source: NHTSA 26V283000.

    Product
    TESLA — 2021 TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V378000·2026-05-05

    [pending] 2023 GRAND DESIGN SOLITUDE

    Pending LLM rewrite. Source: NHTSA 24V378000.

    Product
    GRAND DESIGN — 2023 GRAND DESIGN SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V377000·2026-05-05

    [pending] 2025 LION LIONC

    Pending LLM rewrite. Source: NHTSA 24V377000.

    Product
    LION — 2025 LION LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V301000·2026-05-04

    [pending] 2022 NEWMAR BAY STAR

    Pending LLM rewrite. Source: NHTSA 24V301000.

    Product
    NEWMAR — 2022 NEWMAR BAY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-05042026-01·2026-05-04

    Giovanni Rana Ravioli Pasta Contains Undeclared Shellfish Allergen

    USDA FSIS issued a public health alert for Giovanni Rana ravioli sold at Costco in Maryland and New Jersey. Products labeled as beef and burrata actually contain shrimp in lobster sauce, an undeclared shellfish allergen.

    Product
    Rana Meal Solutions, LLC — FSIS Issues Public Health Alert for Ravioli Pasta With Beef Sauce Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·25V254000·2026-05-04

    [pending] 2025 MERCEDES-BENZ G 580

    Pending LLM rewrite. Source: NHTSA 25V254000.

    Product
    MERCEDES-BENZ — 2025 MERCEDES-BENZ G 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V302000·2026-05-04

    [pending] 2021 MINI COOPER SE

    Pending LLM rewrite. Source: NHTSA 24V302000.

    Product
    MINI — 2021 MINI COOPER SE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V257000·2026-05-04

    [pending] 2022 VOLVO VN

    Pending LLM rewrite. Source: NHTSA 25V257000.

    Product
    VOLVO — 2022 VOLVO VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V304000·2026-05-04

    [pending] 2024 NISSAN SENTRA

    Pending LLM rewrite. Source: NHTSA 24V304000.

    Product
    NISSAN — 2024 NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V129000·2026-05-03

    [pending] 2025 GMC SIERRA 3500

    Pending LLM rewrite. Source: NHTSA 26V129000.

    Product
    GMC — 2025 GMC SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V128000·2026-05-03

    [pending] 2021 TOYOTA HIGHLANDER

    Pending LLM rewrite. Source: NHTSA 26V128000.

    Product
    TOYOTA — 2021 TOYOTA HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V097000·2026-05-02

    [pending] 2023 THOR MOTOR COACH GEMINI

    Pending LLM rewrite. Source: NHTSA 25V097000.

    Product
    THOR MOTOR COACH — 2023 THOR MOTOR COACH GEMINI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V099000·2026-05-02

    [pending] 2022 KIA SOUL

    Pending LLM rewrite. Source: NHTSA 25V099000.

    Product
    KIA — 2022 KIA SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V160000·2026-05-02

    [pending] 2021 JAYCO SWIFT

    Pending LLM rewrite. Source: NHTSA 24V160000.

    Product
    JAYCO — 2021 JAYCO SWIFT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V164000·2026-05-02

    [pending] 2025 INTERNATIONAL HX

    Pending LLM rewrite. Source: NHTSA 24V164000.

    Product
    INTERNATIONAL — 2025 INTERNATIONAL HX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V067000·2026-05-02

    [pending] 2020 JAGUAR I-PACE

    Pending LLM rewrite. Source: NHTSA 26V067000.

    Product
    JAGUAR — 2020 JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V100000·2026-05-02

    [pending] 2024 VOLKSWAGEN ATLAS CROSS SPORT

    Pending LLM rewrite. Source: NHTSA 25V100000.

    Product
    VOLKSWAGEN — 2024 VOLKSWAGEN ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide