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.

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1001–1025 of 26077

  • HighCPSC·26417·2026-04-16

    Electric Pressure Washers Recalled for Electrocution and Shock Hazards

    Patoolio Direct pressure washers sold on Amazon lack a ground-fault circuit-interrupter (GFCI), creating serious electrocution and shock risk. Consumers should stop using them and contact the company for a refund.

    Product
    Patoolio Direct Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26427·2026-04-16

    SpringFlower 5-in-1 Montessori Toy Sets Recalled for Choking Hazard

    SpringFlower 5-in-1 Montessori Toy Sets contain an airplane-shaped teething toy with tentacles that pose a choking hazard to young children. No injuries have been reported.

    Product
    SpringFlower 5-in-1 Montessori Toy Set
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26426·2026-04-16

    Apex Gaming PCs Recalls ATX Computer Power Supplies Due to Electrical Shock Hazard

    Apex Gaming PCs is recalling about 17,730 Manik and Apex-branded ATX computer power supplies sold online from December 2021 through February 2026 due to missing electrical hazard warning labels. Units lack proper warnings about shock and electrocution risks if opened.

    Product
    Manik and Apex-branded ATX Computer Power Supplies (PSU)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26408·2026-04-16

    Sanlebi Pet Vet Playsets Recalled for Battery Ingestion Risk

    The Sanlebi Pet Vet Playset is recalled because button cell batteries in the nail grinder and otoscope can be easily accessed by children. Consumers should immediately remove these components and contact Letokids for a refund or replacement.

    Product
    Sanlebi Pet Vet Playsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26421·2026-04-16

    Fengrong Tool Electric Pressure Washers Recalled for Electrocution Hazard from Missing GFCI

    Fengrong Tool electric pressure washers lack integral GFCI protection, posing serious electrocution risk. About 500 units sold via Amazon from October 2025 through January 2026 for $80–$130. Consumers should stop using immediately and contact Fengrong Tool for refunds.

    Product
    Fengrong Tool Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26425·2026-04-16

    Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risk

    ZOLIQUEX adult portable bed rails sold on Amazon from August 2023 through February 2026 violate federal safety standards due to entrapment hazards that could cause asphyxiation. About 16,000 units were affected.

    Product
    ZOLIQUEX Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26412·2026-04-16

    Macy's Recalls Arch Studio Tea Kettles Over Detachable Handle Burn Hazard

    Macy's is recalling Arch Studio tea kettles because the handle can detach during use when heated, posing a risk of burn injury. About 4,600 kettles were sold nationwide from August 2025 through February 2026.

    Product
    Arch Studio Tea Kettle
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26424·2026-04-16

    LED Finger Beam Lights Recalled Due to Accessible Button Battery Hazard

    ZMC Group is recalling LED Finger Beam Lights because the toy contains easily accessible button cell batteries that children can swallow, risking serious internal chemical burns or death.

    Product
    LED Finger Beam Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26406·2026-04-16

    Electric Pressure Washers Recalled for Serious Shock and Electrocution Risk

    BAYOTAK USA electric pressure washers lack a ground-fault circuit-interrupter (GFCI), creating a serious shock and electrocution hazard. No injuries reported. Consumers should stop using the product and contact the importer for a free replacement.

    Product
    BAYOTAK USA Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26420·2026-04-16

    Agiiman Electric Pressure Washers Recalled for Shock and Electrocution Hazards

    Agiiman Electric Pressure Washers lack ground-fault circuit-interrupter (GFCI) protection, creating a serious risk of electrical shock and electrocution. Consumers should stop using these units immediately and contact Agiiman for a full refund.

    Product
    Agiiman Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26428·2026-04-16

    Pet laser toys recalled for battery ingestion hazard

    Lil' Buddies Pet Laser Toys are recalled by JC Sales for battery ingestion hazard from button cell batteries. About 51,160 units sold from February 2023–November 2025; no injuries reported.

    Product
    Lil' Buddies Pet Laser Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26407·2026-04-16

    Generac Portable Generators recalled due to fire and burn hazards

    Certain Generac portable generators may leak fuel from the carburetor when first filled with gasoline, creating a risk of fire or burn injury. About 149,400 units are affected.

    Product
    Generac Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1728-2026·2026-04-15

    Medline medical convenience kits with defective syringe rotating adaptors recalled

    Medline is recalling 439 medical convenience kits worldwide containing defective NAMIC Angiographic RA Control Syringes. The syringe rotating adaptor may unwind during use, causing loose or full disconnection between the syringe and manifold.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. ROBOTIC PACK, Medline SKU # DYNJ58475F; 2. URO/GEN ROBOTIC PACK, Medline SKU # DYNJ60803J.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1713-2026·2026-04-15

    NAMIC Angiographic Control Syringes recalled for potential adapter disconnection

    Medline's NAMIC Angiographic Control Syringes are being recalled because the rotating adaptor may unwind during use, potentially causing disconnection from the manifold. This Class I recall affects 192,690 units distributed worldwide.

    Product
    NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4. SYRINGE,7,ML,TR/FR,RA,W/RES,OE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0655-2026·2026-04-15

    Red Bull Male Enhancement Supplement Recalled for Undeclared Sildenafil

    The FDA recalled Red Bull Extreme Male Enhancement Supplement distributed in New Jersey due to undeclared sildenafil. The product contains an unlabeled prescription drug ingredient that poses health risks from drug interactions and contraindications.

    Product
    Red Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Red Bull Corporation. Turkey www.redbullhoney.com UPC Code 9554100205595
    Category
    Consumer Product
    Distribution
    0 states
  • SevereFDA (Food)·H-0654-2026·2026-04-15

    Blue Bull Extreme Male Enhancement Supplement Recalled for Undeclared Sildenafil

    Blue Bull Extreme Male Enhancement Supplement has been recalled due to undeclared sildenafil, a prescription pharmaceutical ingredient. The product was distributed in New Jersey.

    Product
    Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Blue Bull Corporation Made In USA. UPC Code 707443349917
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1712-2026·2026-04-15

    NAMIC Angiographic Syringes May Disconnect Due to Adaptor Failure

    NAMIC Angiographic Syringes may have rotating adaptors that unwind during use, causing loose or complete disconnection from the manifold, affecting 2.6 million units distributed worldwide.

    Product
    NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1715-2026·2026-04-15

    Medline Angiographic Syringe Adaptor Kits Recalled for Disconnection Risk

    Medline Industries is recalling 1,698 medical convenience kits containing angiographic syringe adaptors that may unwind during use, causing loose or disconnected connections between components.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. CSTM MANIFOLD KIT - TITUS, Medline SKU VASC1061; 2. CSTM MANIFOLD KIT - FRYE, Medline SKU VASC1074; 3. CRYO EP MANIFOLD KIT, M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1718-2026·2026-04-15

    Angiographic Syringe Adapters May Loosen or Disconnect During Use

    Medline is recalling angiographic syringes because the rotating adapter may unwind during use, causing loose or complete disconnection between the syringe and manifold.

    Product
    NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5. MTO,SYRING
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1727-2026·2026-04-15

    Medline angiographic rotating adaptor control syringes recalled for disconnection risk

    Medline recalled 966 medical convenience kits containing NAMIC control syringes because the syringe rotating adaptor may unwind during use, causing loose or complete disconnection from the manifold.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. DELIVERY PACK, Medline SKU # DYNJ42892F; 2. DELIVERY PACK, Medline SKU # DYNJ42892G.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1723-2026·2026-04-15

    Medline syringe adapter kits recalled for disconnection risk

    Medline medical convenience kits containing NAMIC syringe adaptors may unwind during use, causing loose or disconnected connections. Affected kits have been distributed worldwide.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1717-2026·2026-04-15

    Medline Recalls NAMIC Angiographic Syringes Over Rotating Adaptor Disconnection Risk

    Medline is recalling NAMIC Angiographic Syringes because the rotating adaptor may unwind during use, causing loose or full disconnection from the manifold. The FDA classified this as a Class I recall.

    Product
    NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5. MTO,SYRING
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1724-2026·2026-04-15

    Medline medical procedure kits recalled for syringe adaptor disconnection risk

    Medline is recalling medical procedure kits because the syringe rotating adaptor may unwind during use, potentially causing disconnection between the syringe and manifold.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. MTS RH LFT HRT KIT, Medline SKU # 60010508; 2. MTS 3V W/GUIDE, Medline SKU # 60100701; 3. ANGIOGRAPHY KIT, Medline SKU # 60131
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1714-2026·2026-04-15

    Medical convenience kits recalled for potential syringe adapter disconnection

    Medline recalls 3,120 medical convenience kits containing control syringes due to a potential risk that the rotating adaptor could unwind during use, causing loose or complete disconnection from the manifold.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B
    Category
    Medical Device
    Distribution
    Distributed nationwide