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.

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526–550 of 31574

  • ModerateFDA (Devices)·Z-2654-2026·2026-07-08

    Medline 111 Gravity Set with Needle Free Y-Sites engineering sample recall

    BD Switzerland SARL is recalling a Medline 111 Gravity Set with 3 Needle Free Y-Sites (Catalog Number SAM2461, Lot 25X445) because engineering samples labeled "Not for Human Use" were inadvertently shipped to the U.S. market.

    Product
    MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineering Sample/Not for Human Use
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0697-2026·2026-07-08

    Terpenicol Antifungal Solution Recalled for CGMP Deviations

    Blaine Labs Inc is recalling Terpenicol (Undecylenic Acid) antifungal solution because the firm discontinued required stability testing for products still on the market within their expiration dates.

    Product
    TERPENICOL — TERPENICOL (UNDECYLENIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2669-2026·2026-07-08

    Solar GI System Water Perfusion Units Recalled Due to Moisture Accumulation

    Laborie Medical Technologies is recalling Solar GI System (Water Perfusion) units worldwide because moisture may accumulate in internal tubing and filters under extended use, potentially affecting airflow and pressure measurement performance.

    Product
    Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI H2O, 12p, Trolley system (G3-6), Solar GI HRM H2O, 24p, Compact Pole system (G3-7), Solar GI HRM H2O, 24p, Trolley system (G3-8), Solar GI HRM H2O, 36p, Trolley system (G3-12), Solar GI HRAM H2O, 24p
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2658-2026·2026-07-08

    PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen Medical Device Recall

    Bard Access Systems, Inc. is recalling PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen devices due to lidocaine ampoules manufactured under deficient manufacturing practices by the supplier.

    Product
    CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 Catheter stylets provide internal reinforcement to aid in catheter placement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2641-2026·2026-07-08

    ARTIS icono biplane medical imaging system detector lift malfunction

    Siemens is recalling 85 units of the ARTIS icono biplane (Model 11327600) due to potential loss of detector movement capability when adjusted to maximum or minimum lift height limits.

    Product
    ARTIS icono biplane. Model Number: 11327600.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0699-2026·2026-07-08

    Revitaderm Wound Care Benzalkonium Chloride OTC Drug Recall

    Blaine Labs Inc is recalling Revitaderm Wound Care (Benzalkonium Chloride 0.1%) topical antiseptic gel due to current good manufacturing practice (CGMP) deviations. The product was manufactured in the same facility under the same conditions as a product found to be contaminated.

    Product
    REVITADERM WOUND CARE — REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2668-2026·2026-07-08

    Soft Tissue Biopsy Trays recalled due to deficient manufacturing practices

    Bard Access Systems is recalling soft tissue biopsy trays (models 4380 Economy and 4382A) due to lidocaine ampoules being manufactured under deficient manufacturing practices.

    Product
    4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108501 The Soft Tissue Biopsy devices are indicated for use in the collection of aspirate tissue (e.g. liver, kidney, etc.).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0654-2026·2026-07-08

    Fexofenadine Hydrochloride Tablets 180 mg Recalled for Impurities

    SUN PHARMACEUTICAL INDUSTRIES INC is recalling Fexofenadine Hydrochloride Tablets, USP 180 mg distributed nationwide because the product failed impurities and degradation specifications. The recall affects approximately 9,048 bottles distributed across the United States.

    Product
    Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm Laboratories, Inc., New Brunswick, NJ 08901. NDC 66336-561-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V436000·2026-07-07

    Subaru Ascent, Forester, and Crosstrek vehicles with incorrect weight labels

    Subaru is recalling certain 2019–2026 Ascent, 2025–2026 Forester, and 2026 Crosstrek Hybrid vehicles due to incorrect Gross Axle Weight Rating labels, which may lead to vehicle overload and increased crash risk.

    Product
    SUBARU — 2020 SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V419000·2026-07-06

    [pending] 2025 SUBARU FORESTER

    Pending LLM rewrite. Source: NHTSA 25V419000.

    Product
    SUBARU — 2025 SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V380000·2026-07-05

    [pending] 2024 LAND ROVER RANGE ROVER

    Pending LLM rewrite. Source: NHTSA 24V380000.

    Product
    LAND ROVER — 2024 LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V290000·2026-07-05

    [pending] 2020 JEEP CHEROKEE

    Pending LLM rewrite. Source: NHTSA 26V290000.

    Product
    JEEP — 2020 JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V384000·2026-07-05

    [pending] 2019 HONDA FIT

    Pending LLM rewrite. Source: NHTSA 24V384000.

    Product
    HONDA — 2019 HONDA FIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V289000·2026-07-05

    GMC Yukon and Other GM Vehicles with Transfer Case Defect

    General Motors is recalling certain 2026 GMC Yukon, Sierra 1500, Yukon XL and other GM vehicles, as well as select 2015–2020 models, due to a missing component in the drivetrain transfer case that may cause wheel lockup without warning. The defect increases the risk of a crash.

    Product
    GMC — 2026 GMC YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V172000·2026-07-03

    [pending] 2021 TESLA MODEL X

    Pending LLM rewrite. Source: NHTSA 25V172000.

    Product
    TESLA — 2021 TESLA MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V173000·2026-07-03

    [pending] 2025 INFINITI QX60

    Pending LLM rewrite. Source: NHTSA 25V173000.

    Product
    INFINITI — 2025 INFINITI QX60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26600·2026-07-02

    Junpower CR2032 Lithium Coin Batteries Recalled for Ingestion Hazard

    Junpower CR2032 Batteries (20-piece packs) lack required child-resistant packaging and warning labels. If swallowed, these lithium coin batteries can cause serious internal injuries or death.

    Product
    Junpower CR2032 Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26599·2026-07-02

    Metalux Optimized High Bay LED Light Fixtures Recalled for Fire Hazard

    Cooper Lighting recalls about 42,000 Metalux Optimized High Bay LED light fixtures due to a fire hazard. The LED board can overheat or contact combustible materials; nine fires have been reported with no injuries or property damage.

    Product
    Metalux Optimized High Bay (OHB) LED Light Fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26591·2026-07-02

    VEVOR Baby Loungers Recalled for Entrapment and Fall Hazards

    VEVOR baby loungers sold through multiple retailers from November 2024 through January 2026 are being recalled due to violations of mandatory infant sleep product safety standards. The loungers pose serious risks of fall and entrapment hazards that can cause death or serious injury.

    Product
    VEVOR baby loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26601·2026-07-02

    Metal Wire Bristle Grill Brushes Recalled Over Detachable Bristle Ingestion Hazard

    Conair is recalling about 1.7 million Cuisinart metal wire bristle grill brushes because small wire bristles can detach and be swallowed, posing a risk of serious internal injury. Three consumers have already swallowed bristles and required medical treatment.

    Product
    Metal Wire Bristle Grill Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26593·2026-07-02

    CVS Health Medicated Hemorrhoidal Wipes Lack Child-Resistant Packaging

    CVS Health Medicated Hemorrhoidal Wipes lack required child-resistant packaging despite containing lidocaine, a substance that poses risk of serious injury or death if ingested by young children.

    Product
    CVS Health Medicated Hemorrhoidal Wipes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26596·2026-07-02

    AMASKY Nursing Pillows Recalled for Risk of Suffocation

    AMASKY Nursing Pillows, sold on Amazon from January to March 2026, violate safety standards and can obstruct infant breathing, posing a serious risk of suffocation. No injuries have been reported.

    Product
    AMASKY Nursing Pillows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26598·2026-07-02

    Gigglescape Under the Sea Popping Toy Recalled for Choking Hazard

    Target has recalled approximately 49,000 Gigglescape Under the Sea Popping Toys because the clear plastic dome can detach, exposing small plastic balls that pose a choking hazard. One child began to choke after the dome detached.

    Product
    Gigglescape™ Under the Sea Popping Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26603·2026-07-02

    Roman Candles 8 Shot Fireworks Recalled for Explosion and Burn Hazards

    Winco Fireworks International is recalling Roman Candles 8 Shot 3-Pack firework devices because the fireworks can malfunction and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards. No injuries have been reported.

    Product
    Roman Candles 8 Shot 3-Pack Firework Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26602·2026-07-02

    Unity 7 Shot 200 Gram Aerial Cake Fireworks Recalled for Explosion and Burn Hazard

    Winco Fireworks International recalls Unity 7 Shot 200 Gram Aerial Cake firework devices that can tip over, creating risk of serious injury from explosion and burns. About 87,120 units sold at Pyro City and independent fireworks stores nationwide from January through May 2026 are affected.

    Product
    Unity 7 Shot 200 Gram Aerial Cake Firework Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide