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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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

326–350 of 7486

  • CriticalFDA (Food)·H-0197-2026·2025-11-26

    Whatcom Blue cheese recalled over E coli O103 in raw milk

    Peterson Company is recalling 288 pieces of Twin Sisters Creamery Whatcom Blue cheese due to E. coli O103:H2. The FDA has classified the recall as Class I.

    Product
    Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, product is packed in Cryovac and each package weighs 5oz-6oz. There are 16 pieces per case. This cheese is made from raw milk. Ingredients: cultured raw cow's milk, salt, enzymes, penicillium roqueforti. Made by Twin…
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0195-2026·2025-11-26

    Peppercorn raw milk cheese recalled over E coli O26 contamination

    Twin Sisters Creamery is recalling 115.46 pounds of raw milk Peppercorn cheese due to E. coli O26:H11. The FDA has classified the recall as Class I.

    Product
    Twin Sisters Creamery Peppercorn cheese, 3lb. round cheese wheel, made with raw milk and aged at minimum of 60 days. Ingredients: cultured raw cow's milk, whole peppercorns, salt, enzymes. Made in Ferndale, WA. www.twinsisterscreamery.com.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-0198-2026·2025-11-26

    Farmhouse white cheese recalled over E coli O103 in raw milk

    Peterson Company is recalling 288 pieces of Twin Sisters Creamery Farmhouse White cheese due to E. coli O103:H2. The FDA has classified the recall as Class I.

    Product
    Item# 29608 Farmhouse White, Twin Sisters Creamery brand, product is packed in Cryovac and each package weighs 5oz-6oz. This cheese is made from raw milk. Ingredients: cultured raw cow's milk, salt, enzymes, penicillium roqueforti. Made by Twin Sisters Creamery in Ferndale, WA.…
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0201-2026·2025-11-26

    Lobster bisque recalled over undeclared shrimp in bulk foodservice pouches

    Plenus Group is recalling 659 cases of Rockport Lobster Bisque because the product contains undeclared shrimp. The FDA has classified the recall as Class I.

    Product
    Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Devices)·Z-0430-2026·2025-11-26

    Infusion pump modules recalled because drops can damage the bezel assembly

    CareFusion is recalling 2,574,396 BD Alaris Infusion Pump Modules 8100 because a dropped or jarred pump can suffer bezel damage causing under-infusion, over-infusion or unregulated flow.

    Product
    BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY ONE PIECE BEZEL 8100, REF: 49000270. Used with the following new and updated documents: BD Alaris Infusion System Inspection Safety Reminder, Part: BD-163124, Revision: 00…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0178-2026·2025-11-19

    Peanut butter candy bars recalled over an undeclared cashew allergen

    Zingerman's Coffee Company is recalling 156 units of its 2 oz Peanut Butter Crush Candy Bar over undeclared cashew. The FDA has classified the recall as Class I.

    Product
    Zingerman's Peanut Butter Crush Candy Bar net wt 2oz UPC 844397005237
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Devices)·Z-0451-2026·2025-11-19

    Orthopedic and spine kits recalled over cracked anesthesia circuit tubing

    Medline is recalling ortho spine, total joint and kyphoplasty convenience kits after complaints of anesthesia circuit leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Convenience kits; DYNJ901047R ORTHO SPINE FUMICH DYNJ902308K TOTAL JOINT DYNJ909111F DR SALMA'S SPINE DYNJ909117G PATTERSON TOTAL JOINT DYNJ909113F KYPHOPLASTY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0444-2026·2025-11-19

    Open heart and vascular kits recalled over cracked anesthesia circuit tubing

    Medline is recalling open heart supplement and vascular kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; OPEN HEART SUPPLEMENT DYNJ909116D; VASCULAR DYNJ909124F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0174-2026·2025-11-19

    Italian parsley recalled over potential Salmonella contamination in eight states

    Pacific International Marketing is recalling 308 cases of conventional Italian parsley over potential Salmonella contamination. The FDA has classified the recall as Class I.

    Product
    Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL MARKETING SALINAS, CA 93912 Carton Sticker Label: Conv Italian Parsley 60 Ct Ctn Pacific Product of USA Distributed By: Dynasty Farms Salinas, CA 93905 UPC 40695 80125 Twist Tie (for bunches) Label: FLAT PARSLEY PLU…
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Devices)·Z-0448-2026·2025-11-19

    Urology and hip pinning kits recalled over cracked anesthesia circuit tubing

    Medline is recalling ortho spine, urology minor, set up and hip pinning convenience kits after complaints of anesthesia circuit leaks from cracked tubing. The FDA classified it Class I.

    Product
    Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR DYNJ909132F SET UP DYNJ909308D HIP PINNING
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0187-2026·2025-11-19

    Red Bali kratom powder recalled over potential Salmonella contamination

    Lotus Vaping Technologies is recalling Monarch Premium Kratom Red Bali powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.

    Product
    Monarch Premium Kratom Red Bali powder is packaged in seal mylar pouches: Monarch Premium Kratom Red Bali, 4oz powder (112g), UPC 851006008442 Monarch Premium Kratom Red Bali, 8oz powder (224g), UPC 706970483859 Monarch Premium Kratom Red Bali, 2oz powder (56g), UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0179-2026·2025-11-19

    Cashew candy bars recalled over an undeclared peanut allergen

    Zingerman's Coffee Company is recalling 78 units of its 2 oz Ca$hew Cow Candy Bar over undeclared peanut. The FDA has classified the recall as Class I.

    Product
    Zingerman's Ca$hew Cow Candy Bar net wt 2oz UPC 844397000157
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-0188-2026·2025-11-19

    White Elephant kratom powder recalled over potential Salmonella contamination

    Lotus Vaping Technologies is recalling Monarch Premium Kratom White Elephant powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.

    Product
    Monarch Premium Kratom White Elephant powder is packaged in seal mylar pouches: Monarch Premium Kratom, White Elephant, 4oz powder (112g), UPC 851006008480 Monarch Premium Kratom, White Elephant, 0.5oz powder (14g), UPC 851006008756 Monarch Premium Kratom, White Elephant, 8oz…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0434-2026·2025-11-19

    Detachable brain aneurysm coils recalled because they may fail to detach

    Cerenovus is recalling 12,004 CEREPAK Detachable Coil System units because the coils may fail to detach, which could result in hemorrhagic and ischemic stroke. The FDA classified it Class I.

    Product
    CEREPAK Detachable Coil System - Name/REF: UNIFORM 2MM X 2.5 CM/FCX100202, UNIFORM 2.5MM X 3.3 CM/FCX100253, UNIFORM 3MM X 5.4 CM/FCX100305, UNIFORM 3.5MM X 6.6 CM/FCX100356, UNIFORM 4MM X 7.5 CM/FCX100407, UNIFORM 4MM X 11.5 CM/FCX100412, UNIFORM 5MM X 9.7 CM/FCX100509, UNIFORM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0200-2026·2025-11-19

    Clamshell peach salsa recalled over Listeria risk from supplied peaches

    JFE Franchising is recalling 177 units, 154.88 pounds, of 16 oz peach salsa in clamshells because the peaches supplied by Moonlight Peaches are potentially contaminated with Listeria.

    Product
    Peach Salsa - $5.99-16 oz 639123940636 packaged in clear plastic clamshells Sell by 11/3/2025 Sell by 11/4/2025
    Category
    Food
    Distribution
    18 states
  • CriticalFDA (Devices)·Z-0447-2026·2025-11-19

    Surgical convenience kits recalled over cracked anesthesia circuit tubing

    Medline is recalling 96,406 breast and hernia convenience kits after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Convenience Kit, BREAST HERNIA DYNJ909125G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0443-2026·2025-11-19

    Breathing kits recalled over cracks in the expandable anesthesia tubing

    Medline is recalling the latex-free Breathing Kit DYNJ10550 after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; BREATHING KIT-LF DYNJ10550
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0449-2026·2025-11-19

    Expandable anesthesia circuits recalled over cracks causing leaks in tubing

    Medline is recalling the 120-inch latex-free ExtendFlex anesthesia circuit after complaints of leaks caused by cracks in the expandable tubing. The FDA has classified it Class I.

    Product
    Anesthesia circuit kit; CIRCUIT,ANES,EXTENDFLEX,120,LF DYNJAA10230
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0431-2026·2025-11-19

    MRI upgrade recalled over ice blockage in helium venting paths

    Siemens Medical Solutions is recalling four MAGNETOM Cima.X Upgrade systems because an ice blockage may form in the magnet's helium venting paths. The FDA has classified it Class I.

    Product
    MAGNETOM Cima.X Upgrade. Model Number: 11689304.
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Food)·H-0176-2026·2025-11-19

    Thirty count parsley cases recalled over potential Salmonella contamination

    Pacific International Marketing is recalling 2 cases of 30-count iceless conventional Italian parsley over potential Salmonella. The FDA has classified the recall as Class I.

    Product
    Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL MARKETING SALINAS, CA 93912 PRODUCE OF U.S.A. Sticker Label: Conv Italian Parsley 30 Ct Iceless Pacific Product of USA Distributed By: Dynasty Farms Salinas, CA 93905 Twist Tie (for bunches) Label: FLAT PARSLEY PLU…
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Devices)·Z-0450-2026·2025-11-19

    Robotic surgery kits recalled over cracked anesthesia circuit tubing

    Medline is recalling GYN Robotic and Robotic Prostate convenience kits after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Convenience kits; DYNJ901046M GYN ROBOTIC DYNJ909120D ROBOTIC PROSTATE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0186-2026·2025-11-19

    Green Maeng Da kratom powder recalled over potential Salmonella contamination

    Lotus Vaping Technologies is recalling Monarch Premium Kratom Green Maeng Da powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.

    Product
    Monarch Premium Kratom Green Maeng Da powder is packaged in seal mylar pouches: Monarch Premium Kratom Green Maeng Da, 4oz powder (112g), UPC 851006008466 Monarch Premium Kratom Green Maeng Da, 0.5oz powder (14g), UPC 851006008770 Monarch Premium Kratom Green Maeng Da…
    Category
    Food
    Distribution
    Distributed nationwide