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 the agency’s own highest classification or reported deaths or serious injuries, 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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151–175 of 39702

  • SevereCPSC·27013·2026-10-01

    Golden Resale Recalls Portable Camping Showers Due to Fire Hazard

    Golden Resale is recalling portable camping showers with immersion heaters because they can ignite when out of water, posing a risk of serious injury or death.

    Product
    Portable Camping Showers with bucket and immersion heater
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27014·2026-10-01

    Agrish Adult Portable Bed Rails Recalled for Entrapment and Fall Hazards

    Agrish is recalling adult portable bed rails due to risks of entrapment, asphyxiation, and falls. Consumers should stop using the products and contact the company for a refund.

    Product
    Agrish Adult Portable Bed Rails, models 12014, AG-12011 and 12016
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27008·2026-10-01

    GBYMIUY Recalls Magnetic Stick Figure Toys Due to Ingestion Hazard

    GBYMIUY is recalling magnetic stick figure toy sets because loose high-powered magnets pose a risk of serious injury or death if swallowed by children.

    Product
    GBYMIUY Magnetic Stick Figure Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27003·2026-10-01

    ABC Trading Recalls Squishy Toys Due to Water Bead Ingestion Risk

    ABC Trading is recalling squishy dumpling and crazy squib ball toys because the water beads inside can expand and pose a deadly ingestion hazard to children.

    Product
    Squishy Dumpling Toys, Crazy Squib Ball Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E068000·2026-10-01

    Kuat Pivot V3 Swing-Away Hitch Adapter Recall for Weld Cracking

    Kuat Innovations is recalling Pivot V3 swing-away hitch adapters because a weld may crack, causing the cross beam to detach and create a road hazard.

    Product
    EQUIPMENT:MECHANICAL:CARRIER/RACK recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·27007·2026-10-01

    Designs Direct Recalls Three-Light Floor Lamps Due to Fire and Burn Hazards

    Designs Direct is recalling Cupcakes and Cashmere brand floor lamps because the cord or wiring can overheat, posing fire and burn risks. Consumers should stop using the lamps and request a refund.

    Product
    Designs Direct Cupcakes and Cashmere Brand Three-Light Floor Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-3194-2026·2026-09-30

    AVID Medical Recalls Halyard IV Start Kits Due to Mold Contamination

    AVID Medical is recalling Halyard IV Start Kits because they contain applicators potentially contaminated with Aspergillus penicillioides.

    Product
    Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1390-2026·2026-09-30

    Evergreen Fresh Sprouts Recalls Broccoli Sprouts Due to Salmonella Risk

    Evergreen Fresh Sprouts LLC is recalling broccoli sprouts in Washington due to a potential Salmonella contamination risk.

    Product
    Evergreen Fresh Sprouts LLC, Broccoli Sprouts, packaged in clear plastic zip lock bag, net wt. 4oz, UPC 8 38796 00105 1. Firm distributed cases (6/4oz. bags per case) to distributor.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-1396-2026·2026-09-30

    Bettergoods Lemon Alfredo Fettuccine Recalled for Listeria Contamination

    GIAS FOOD INC. is recalling Bettergoods Lemon Alfredo Fettuccine due to Listeria monocytogenes contamination. Consumers should stop eating the product and return it to Walmart.

    Product
    Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 20 2027 L6080C, UPC 194346442706, DISTRIBUTED BY: Walmart Inc.…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0862-2026·2026-09-30

    Sterling Recalls Carboxymethylcellulose Sodium Eye Drops Due to Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling specific lots of Cameron Pharmaceuticals Carboxymethylcellulose Sodium 0.5% Eye Lubricant due to a lack of assurance of sterility.

    Product
    Lubricant Eye Drops-Cameron Pharmaceuticals, Carboxymethylcellulose Sodium 0.5%, Eye Lubricant, 0.5 FL OZ (15 mL) bottles, Distributed by Cameron Pharmaceuticals, LLC, Louisville, KY, 40245, NDC 42494-448-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3139-2026·2026-09-30

    CooperSurgical Recalls Infant Nasal CPAP Tubing Due to Loose Connection Risk

    CooperSurgical is recalling specific lots of INCA Infant Nasal CPAP tubing because a loose connection may cause loss of pressure and reduced oxygenation.

    Product
    INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set. Stay-Flex tubing component. 5 units per box. Model Numbers: 44-2707, 44-2709, 44-2710, 44-2712, 44-2715.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0858-2026·2026-09-30

    Walgreens Lubricant Eye Drops Recalled for Sterility Assurance Concerns

    Sterling Pharmaceutical Services LLC is recalling Walgreens Lubricant Eye Drops due to a lack of assurance of sterility. The recall affects 199,600 packs distributed nationwide.

    Product
    WALGREENS LUBRICANT EYE DROPS — WALGREENS LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V628000·2026-09-30

    Grech Motorhomes Recalled for Rooftop Fan Fire Risk

    Grech is recalling 2026-2027 Strada, Terreno, and Turismo motorhomes because a rooftop ventilation fan circuit board may overheat and cause a fire.

    Product
    GRECH — GRECH TURISMO, STRADA, TERRENO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V627000·2026-09-30

    Highland Ridge Range Lite Air Travel Trailer Fresh Water Tank Recall

    Highland Ridge RV is recalling 2022-2024 Range Lite Air travel trailers because fastener failure may cause the fresh water tank to detach, creating a road hazard.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT RANGE LITE AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1395-2026·2026-09-30

    Whole Foods Market Recalls Cabricharme Cheese for Undeclared Egg Allergen

    Whole Foods Market is recalling Cabricharme cheese sold in several states due to an undeclared egg allergen. Consumers should check their refrigerators and discard or return the product.

    Product
    Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf life: 30 days, all dates through and including 10/7/2026 Packaging: Plastic wrapped by slice Net Wt.: Various, cut from whole wheel and priced by weight with Whole Foods Market scale label PLUs: 54670, 57953
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0856-2026·2026-09-30

    Sodium Chloride Ophthalmic Solution Recalled for Sterility Assurance Issues

    Sterling Pharmaceutical Services is recalling Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, due to a lack of assurance of sterility.

    Product
    SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5% — SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5% (SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5%)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0859-2026·2026-09-30

    Sterling Pharmaceutical Recalls Lubricating Tears Due to Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling specific lots of Lubricating Tears because the company cannot guarantee the product is sterile.

    Product
    LUBRICATING TEARS — LUBRICATING TEARS (CARBOXYMETHYLCELLULOSE SODIUM 0.5% SOLUTION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0860-2026·2026-09-30

    Gentle Eyes Lubricant Eye Drops Recalled for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling Gentle Eyes Lubricant Eye Drops due to a lack of assurance of sterility.

    Product
    GENTLE EYES LUBRICANT EYE DROPS — GENTLE EYES LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0861-2026·2026-09-30

    Sterling Recalls Major LubriFresh P.M. Ointment for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling Major LubriFresh P.M. Nighttime Ointment due to a lack of assurance of sterility. The recall covers 34,368 tubes distributed nationwide.

    Product
    Major LubriFresh P.M. Nighttime Ointment, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1391-2026·2026-09-30

    United and Good & Gather Light Brown Sugar Recalled for Wheat Contamination

    United Sugar Producers and Refiners is recalling specific batches of United and Good & Gather light brown sugar due to potential wheat kernel contamination.

    Product
    Light Brown Sugar, Packaged in he follow configurations: 1. United, Net Wt. 50 lbs., (22.68kg). Item Number 810051. Distributed By: United Sugar Producers & Refiners, Minneapolis, MN 55439. 2. Good & Gather, Net Wt 2 lb. (32 oz) 907g. Item Number 817773. UPC 0…
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0863-2026·2026-09-30

    AvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution due to a lack of assurance of sterility.

    Product
    CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3266-2026·2026-09-30

    Medline Neurological Sponges Recalled for Potential Endotoxin Variability

    Medline Industries is recalling 128 Major Pack Convenience Kits containing neurological sponges due to potential endotoxin variability that may cause adverse health events.

    Product
    Medline Convenience Kits: 1) MAJOR PACK, Catalog Number: DYNJ81325A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3244-2026·2026-09-30

    Olympus BiCOAG Hemostasis Probe Recall Due to Ceramic Tip Detachment Risk

    Olympus is recalling 404 BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.

    Product
    Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD-B610LA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0855-2026·2026-09-30

    AvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% due to a lack of assurance of sterility.

    Product
    CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide