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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6926–6950 of 89525

  • SevereCPSC·25312·2025-06-05

    ZRWD Infant Swings Recalled for Suffocation and Battery Hazards

    ZRWD infant swings (model S0008A) sold on Amazon are recalled due to suffocation risk from incline angles exceeding safety limits and missing battery hazard warnings. About 3,540 units are affected.

    Product
    ZRWD Infant Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25325·2025-06-05

    HTP residential gas boilers recalled due to fire and carbon monoxide hazard

    HTP-brand ELU Elite Ultra residential gas boilers are being recalled because the boiler door can fail to seal properly, allowing flames and gases to escape, posing fire and carbon monoxide poisoning hazards that can result in death or serious injury.

    Product
    HTP residential gas boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V378000·2025-06-05

    Honda CR-V Hybrid fuel feed hose may be improperly installed

    Honda is recalling certain 2025 CR-V Hybrid vehicles because the fuel feed hose may have been improperly installed, allowing fuel to leak. This fails FMVSS 301.

    Product
    HONDA — HONDA CR-V HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25322·2025-06-05

    Apollo America Combination Smoke and Carbon Monoxide Detectors Recalled

    Apollo America 51000-600 combination smoke and carbon monoxide detectors can malfunction and fail to alert users to fire or CO leaks, risking smoke inhalation, CO poisoning, or death. Vivint is sending free replacement detectors to all known purchasers.

    Product
    Apollo America 51000-600 Combination Smoke and Carbon Monoxide Detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25315·2025-06-05

    ZHORANGE Portable Bassinets Recalled for Fall Hazard Risk

    ZHORANGE portable bassinets (model 148012-A) are recalled due to sides that are too low and absence of a stand, creating a fall hazard for infants. The product violates federal safety standards for infant sleep products.

    Product
    ZHORANGE Portable Bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25321·2025-06-05

    Yamaha Golf Car Vehicles Recalled Due to Accelerator Pedal Spring Failure

    Yamaha is expanding a recall of approximately 352,000 golf car vehicles because the accelerator pedal spring can fail to return to idle, posing a crash hazard. No injuries have been reported to date.

    Product
    Yamaha Golf Car Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25320·2025-06-05

    Midea Recalls 1.7 Million U and U+ Window Air Conditioners Due to Mold Exposure Risk

    Midea is recalling about 1.7 million U and U+ Window Air Conditioners because pooled water can fail to drain quickly, allowing mold to grow. At least 152 mold reports exist, including 17 reports of consumers experiencing respiratory infections, allergic reactions, coughing, sneezing, and sore throats.

    Product
    U and U+ Window Air Conditioners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25319·2025-06-05

    Specialized Globe-Branded Haul ST and LT E-Bikes Recalled for Fall Hazard

    Specialized Bicycle Components is recalling about 11,100 Globe-branded Haul ST and LT e-bikes due to a telescopic seat post that can break when fully extended, creating a fall hazard. The company has received 13 incident reports including two minor injuries.

    Product
    Haul ST and LT E-bikes with telescopic seat posts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V366000·2025-06-05

    Mercedes-Benz EQE and EQS vehicles recalled for defective pedestrian alert software

    Mercedes-Benz is recalling certain 2022–2025 S-Class, EQE, EQE SUV, EQS, and EQS SUV vehicles because the Acoustic Vehicle Alerting System (AVAS) software may produce an incorrect warning sound while reversing, potentially failing to alert pedestrians.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH EQS 450+, EQS 580 4MATIC, EQS SUV 580 4MATIC, EQS SUV 450 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25314·2025-06-05

    Hobby Toy Hammer Ball Sets Recalled for Choking Hazard Risk

    Hobby Toy Hammer Ball sets sold on Amazon contain small balls that violate federal toy safety regulations for children under three and pose a choking hazard. About 2,000 units sold from September 2024 through April 2025 are affected.

    Product
    Hobby Toy Hammer Ball sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25324·2025-06-05

    Direct Scaffold Supply Baker Scaffolding Casters Recalled for Fall Hazard

    Direct Scaffold Supply is recalling casters used in multi-purpose baker style scaffolding due to faulty spot welds that can cause caster failure and scaffolding instability, creating a fall hazard. One injury from a caster failure has been reported.

    Product
    Casters on Direct Scaffold Supply Multi-Purpose Baker Style Scaffolding Products
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25323·2025-06-05

    DR Power Equipment Battery-Powered Chainsaws Recalled for Fire and Burn Hazards

    DR Power Equipment battery-powered chainsaws are being recalled because the motor controller can overheat during operation, posing fire and burn hazards. About 7,180 units were distributed nationwide.

    Product
    Battery-Powered Chainsaws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25313·2025-06-05

    Rinnai i-Series Plus Gas Boilers Recalled for Carbon Monoxide Hazard

    Rinnai America is recalling about 2,030 i-Series Plus gas boilers because the door can fail to seal properly due to incorrect screws, allowing carbon monoxide to escape. No injuries have been reported.

    Product
    Rinnai i-Series Plus gas boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0451-2025·2025-06-04

    Carvedilol Tablets 25 mg Recalled Due to Impurity Above Acceptable Limit

    Glenmark Pharmaceuticals is recalling Carvedilol Tablets USP 25 mg nationwide due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit, resulting from CGMP deviations.

    Product
    CARVEDILOL — CARVEDILOL (CARVEDILOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0450-2025·2025-06-04

    Carvedilol Tablets 12.5 mg Recalled for Impurity Above Limit

    Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 12.5 mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit, resulting from current Good Manufacturing Practice (CGMP) deviations.

    Product
    CARVEDILOL — CARVEDILOL (CARVEDILOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1818-2025·2025-06-04

    ELEOS Collar Stem 15mm mistakenly labeled as 13mm modular stem

    Onkos Surgical is recalling ELEOS Collar Stem components (Model HC-15120-03M) that were packaged and labeled as 13mm modular segmental stems when they are actually 15mm in diameter. This mislabeling could result in implantation of an incorrectly-sized component during limb salvage surgery.

    Product
    ELEOS COLLAR STEM, CEMENTED, FLUTED, 15MM X 120MM. Model Number: HC-15120-03M. Component of Limb Salvage System with BioGrip.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1817-2025·2025-06-04

    ELEOS Collar Stem Cemented Fluted Implant Size Mislabeling Recall

    Onkos Surgical is recalling 23 units of ELEOS Collar Stem implants (Model HC-13120-03M) because packages labeled as 13mm contained 15mm diameter implants instead, creating a risk of implant mismatch during surgery.

    Product
    ELEOS COLLAR STEM, CEMENTED, FLUTED, 13MM X 120MM. Model Number: HC-13120-03M. Component of Limb Salvage System with BioGrip.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0448-2025·2025-06-04

    Carvedilol Tablets Recalled Due to N-Nitroso Impurity

    Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 3.125mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit. The recall affects 100-count and 500-count bottles distributed nationwide.

    Product
    CARVEDILOL — CARVEDILOL (CARVEDILOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0822-2025·2025-06-04

    Tomato 3 Count recalled due to potential Salmonella contamination

    Williams Farms Produce Sales Co., Inc. is recalling Tomato 3 Count products (UPC 0 33383 65504 8) distributed to GA, NC, and SC because the product may contain Salmonella.

    Product
    Tomato 3 Count UPC 0 33383 65504 8, 10lb box, 25lb box & 60ct/2 layer box Williams Farms Repack, LLC Lodge, SC 29082
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·25V374000·2025-06-04

    Triple E Recalls 2025 Motorhomes Due to Wiring Insulation Defect

    Triple E is recalling 2025 Wonder and Unity motorhomes because incorrectly installed inverter wiring insulation may overheat, increasing the risk of fire.

    Product
    TRIPLE E RV — TRIPLE E RV, TRIPLE E WONDER, UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0453-2025·2025-06-04

    Endurance Boost With Horny Goat Weed Supplement Recalled for Undisclosed Drug Content

    VEPEMVA Nutrition's Endurance Boost with Horny Goat Weed has been recalled because it contains Sildenafil and Propoxyphenylsildenafil, undisclosed active pharmaceutical ingredients. The product was marketed and sold without FDA approval.

    Product
    ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8N
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0449-2025·2025-06-04

    Carvedilol Tablets 6.25 mg Recalled for N-Nitroso Impurity

    Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 6.25 mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit. The recall affects 100-count and 500-count bottles distributed nationwide.

    Product
    CARVEDILOL — CARVEDILOL (CARVEDILOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1860-2025·2025-06-04

    DORO Easy-Connect Navigation Adaptor compatibility issue recall

    Pro-Med Instruments is recalling the DORO Easy-Connect Navigation Adaptor due to potential compatibility problems that could affect positioning accuracy and navigation system function. The company distributed 217 units worldwide.

    Product
    DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)
    Category
    Medical Device
    Distribution
    Distributed nationwide