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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401–425 of 5601

  • CriticalFDA (Food)·F-0578-2025·2025-03-05

    Gerber Baby Teething Sticks Recalled Due to Choking Risk

    Nestlé-USA is recalling all lots of Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Strawberry Apple flavor following complaints of infant choking. The product was distributed across 42 states and Puerto Rico.

    Product
    Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER PRODUCTS CO., FREMONT, MI 49413
    Category
    Food
    Distribution
    45 states
  • SevereNHTSA·24V345000·2025-03-05

    BMW 2024-2025 X5, X6, X7, XM, and Alpina XB7 Seat Belt Detection System Defect

    BMW recalls certain 2024-2025 X5, X6, X7, XM, and Alpina XB7 models due to a seat belt detection system defect that may fail to alert drivers of unbuckled passengers or allow proper deployment of the supplemental restraint system.

    Product
    BMW — 2025 BMW X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0572-2025·2025-03-05

    Mombo's Vanilla Soft Serve Ice Cream Mix Recalled for Undeclared Egg Allergen

    Arizona Foods Group is recalling Mombo's Vanilla Soft Serve Ice Cream Mix because it may contain egg, an undeclared allergen. Consumers with egg allergies should not consume this product.

    Product
    FOOD SERVICE - Mombo s Vanilla Soft Serve Ice Cream Mix, frozen & thawed for Ice cream machines. Packaged in a half gallon carton 64 oz and placed in cases of 6-units. Shelf-life is 18 months frozen / 30 days thawed refrigerated. Carton is a plain white carton with a sticker
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1196-2025·2025-03-05

    Ventec VOCSN Ventilators Recalled Due to Incorrect Service Parts

    Ventec Life Systems recalled VOCSN Multi-Function Ventilators (30 units in CA, NY, MO) due to incorrect parts used during service. Defects may cause unexpected shutdown or impaired respiratory monitoring and support.

    Product
    VOCSN Multi-Function Ventilators: VOCSN+Pro (V+O+C+S+N+Pro, English), REF: PRT-00490-001; V+Pro (V+Pro, English), REF: PRT-01185-000, PRT-01185-002
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Food)·F-0577-2025·2025-03-05

    Garden Salad Recalled for Undeclared Peanut Allergen in Florida and Georgia

    FRESHPOINT CENTRAL FLORIDA, INC. is recalling Garden Salad 5 oz packages due to undeclared peanut allergen. The affected product was distributed in Florida and Georgia.

    Product
    Garden Salad 5 oz Lot # 6620223 Best By: 02.05, UPC 766375733300
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0579-2025·2025-03-05

    Gerber Baby Soothe 'n' Chew Teething Sticks Recalled for Choking Risk

    Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Banana flavor are recalled nationwide due to complaints of infant choking. All lots in both 1.59 oz and 3.2 oz packages are affected.

    Product
    Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g) box UPC 0 15000 04608 8 and NET WT 1.59 oz box UPC 0 15000 01015 7 GERBER PRODUCTS CO., FREMONT, MI 49413
    Category
    Food
    Distribution
    45 states
  • SevereNHTSA·24V205000·2025-03-03

    2024 Genesis GV70 Transmission Recall Due to Water Intrusion Risk

    Certain 2024 Genesis GV70 vehicles are recalled because water may leak into the transmission control harness, causing electrical shorts that shift the transmission from Park to Neutral, risking vehicle rollaway.

    Product
    GENESIS — 2024 GENESIS GV70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25157·2025-02-27

    Gas boilers recalled for carbon monoxide poisoning risk; two deaths reported

    Triangle Tube is recalling approximately 60,000 Prestige and Aerco Esteem gas boilers due to carbon monoxide release hazard. Two deaths and 25 CO leak incidents have been reported.

    Product
    Prestige Solo, Prestige Excellence, and Aerco Esteem condensing gas boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25165·2025-02-27

    TRUBLUE auto belay systems recalled due to fall hazard risk

    Head Rush Technologies is recalling approximately 410 TRUBLUE auto belay devices sold online from May 2023 through December 2024 because they can fail to retract, posing a fall hazard. One incident resulted in a fractured leg.

    Product
    TRUBLUE iQ and TRUBLUE iQ+ Auto Belays
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25159·2025-02-27

    Goal Zero Solar Series Combiner Cables Recalled for Fire Hazard

    Goal Zero LLC is recalling about 530 Solar Series Combiner Cables that can malfunction with Nomad-series solar panels and pose a fire hazard. The company has received two reports of fires involving property damage.

    Product
    Goal Zero Solar Series Combiner Cables for Solar Panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1152-2025·2025-02-26

    Philips Allura Xper Patient Table Mattress Defect Fall Risk

    Philips is recalling the Allura Xper FD10C patient examination table due to a mattress defect that may allow patients to fall from the table. The device was distributed worldwide.

    Product
    Allura Xper FD10C; Catalog number: 722001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1070-2025·2025-02-26

    Vascular Tack Endovascular System recalled for deployment and migration risks

    Spectranetics' Intact Vascular Tack Endovascular System may fail to deploy properly or migrate in blood vessels, potentially causing ischemia and requiring additional intervention.

    Product
    Intact Vascular Tack Endovascular System, to treat vascular dissections with Tack implant(s) following angioplasty: (4F,1.5-4.5mm), 150cm, REF: 154150041; Tack, 4F Gen 1.5, 150cm CE, REF: 154150042; Tack, 4F Gen 1.5, 90cm CE, REF: 154090042 (6F, 3.5 - 6.0mm), 135cm, REF: 15613
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1144-2025·2025-02-26

    Allura Xper FD20 Fluoroscopy Table Mattress Issue Causes Fall Risk

    Philips recalls Allura Xper FD20 fluoroscopy patient tables due to a mattress issue that may cause patients to fall during procedures.

    Product
    Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1156-2025·2025-02-26

    Philips Azurion 5 M20 tables recalled due to patient fall risk

    Philips is recalling Azurion 5 M20 imaging tables worldwide due to a mattress defect that could cause patients to fall from the table. This FDA Class I recall involves 632 units.

    Product
    Azurion 5 M20; Catalog numbers: (1) 722228, (2) 722232 (OUS ONLY), (3) 722281 (OUS ONLY).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1147-2025·2025-02-26

    Operating room table recalled due to mattress-related patient fall risk

    Philips Allura Xper FD20 OR Table units (catalog numbers 722023, 722035) are recalled due to a mattress defect that could cause patients to fall during procedures.

    Product
    Allura Xper FD20 OR Table; Catalog numbers: (1) 722023, (2) 722035.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0230-2025·2025-02-26

    Phenylephrine HCl Injection Recall Due to Particulate Matter

    Provepharm Inc. is recalling Phenylephrine HCl Injection vials (Lot 24020027) due to the presence of particulate matter. The affected medication was distributed nationwide.

    Product
    Phenylephrine HCl Injection, USP 100 mg/10 mL (10 mg/mL) vials, Rx only, Pharmacy Bulk Package (supplied as a single unit), Dist. by: Provepharm, Inc., Collegeville, PA 19426
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1143-2025·2025-02-26

    Philips Allura Xper Fluoroscopy Device Patient Table Mattress Fall Risk

    Philips Medical is recalling certain Allura Xper FD10/10 fluoroscopy systems because the patient table mattress could cause patients to fall during procedures. The recall affects devices worldwide.

    Product
    Allura Xper FD10/10; Catalog numbers: (1) 722005, (2) 722011, (3) 722027.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0564-2025·2025-02-26

    Paras Premium Golden Raisins Recalled for Undeclared Sulfites

    Paras Premium Golden Raisins are being recalled due to undeclared sulfites (56.8mg per serving), which can cause serious allergic reactions in sensitive individuals.

    Product
    Paras Premium Golden Raisins; 7 oz and 14 oz; INGREDIENTS: RAISINS; ALLERGEN STATEMENT: Processed in a gluten-free and peanut-free plant; UPC: 818051014811 and 818051014828
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1158-2025·2025-02-26

    Philips Azurion 7 B20 imaging system patient fall hazard from table mattress

    Philips Azurion 7 B20 imaging systems are recalled because the patient table mattress may allow patients to fall. This FDA Class I recall affects 1,314 units distributed worldwide.

    Product
    Azurion 7 B20; Catalog numbers: (1) 722068, (2) 722226, (3) 722236.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1150-2025·2025-02-26

    Philips Allura Xper FD20/20 Imaging Table Mattress Recall

    Philips is recalling 114 units of the Allura Xper FD20/20 imaging table due to mattress defects that could cause patients to fall. 33 units are in the US; 81 are internationally distributed.

    Product
    Allura Xper FD20/20; Catalog numbers: 722038
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1160-2025·2025-02-26

    Azurion 7 M20 Patient Tables Recalled for Patient Fall Risk

    Philips recalls Azurion 7 M20 patient tables due to a mattress defect that could cause patients to fall. Approximately 1,480 units in the US and 2,741 units overseas are affected.

    Product
    Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1149-2025·2025-02-26

    Philips recalls Allura patient table mattress due to fall hazard

    Philips is recalling Allura Xper patient table mattresses because a defect could cause patients to fall. The recall involves 302 units distributed globally.

    Product
    Allura Xper FD20/15; Catalog numbers: 722058
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1157-2025·2025-02-26

    Philips Azurion 7 B12 examination tables recalled due to patient fall risk

    Philips Medical Systems is recalling Azurion 7 B12 examination tables due to a mattress-related patient fall risk. The recall affects 602 total units, including 94 in the US and 508 internationally.

    Product
    Azurion 7 B12; Catalog numbers: (1) 722067, (2) 722225, (3) 722235 (OUS ONLY).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1154-2025·2025-02-26

    Philips Azurion 3 M15 Patient Tables Recalled for Patient Fall Risk

    Philips recalls Azurion 3 M15 imaging tables due to mattress defects that could cause patients to fall from the examination table.

    Product
    Azurion 3 M15; Catalog numbers: (1) 722064, (2) 722222 (3) 722280(OUS ONLY).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1155-2025·2025-02-26

    Philips Azurion 5 M12 Patient Table Recalled for Fall Risk

    Philips Medical Systems is recalling Azurion 5 M12 imaging tables due to a mattress defect that could allow patients to fall from the table.

    Product
    Azurion 5 M12; Catalog numbers: (1) 722227, (2) 722231 (OUS ONLY).
    Category
    Medical Device
    Distribution
    Distributed nationwide