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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226–250 of 7486

  • CriticalFDA (Devices)·Z-0913-2026·2025-12-24

    Anesthesia systems recalled over potential unexpected shutdown on mains power loss

    GE Medical Systems is recalling 1,277 Carestation anesthesia systems over potential unexpected shutdown if AC mains power is unplugged or fails. The FDA has classified the action as Class I.

    Product
    GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1 REF 1012-9620-000; Carestation 620 A1, REF 1012-9620-200; Carestation 620 A1, REF 1012-9620-202; Carestation 620 SE A1, REF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0311-2026·2025-12-24

    Dried salted smelts recalled over Clostridium botulinum in uneviscerated fish

    MAMTAKIM is recalling 45 cases of Belevini Korushka dried salted whole smelts over Clostridium botulinum in uneviscerated fish. The FDA has classified the action as Class I.

    Product
    Belevini KORUSHKA, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK, 20 PACKAGES PER CASE, FROZEN, REFRIGERATE AFTER OPENING
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0312-2026·2025-12-24

    Dried salted bichki smelts recalled over Clostridium botulinum in uneviscerated fish

    MAMTAKIM is recalling 4 cases of Belevini Bichki dried salted whole smelts over Clostridium botulinum in uneviscerated fish. The FDA has classified the action as Class I.

    Product
    Belevini BICHKI, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK,20 PACKAGES PER CASE, FROZEN, REFRIGERATE AFTER OPENING
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-0915-2026·2025-12-24

    Anesthesia power management boards recalled over potential unexpected system shutdown

    GE Medical Systems is recalling 203 Carestation anesthesia system Power Management Board field replaceable units over potential unexpected shutdown if AC mains power is lost.

    Product
    GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replaceable Unit (FRU), 2076139-001-S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0885-2026·2025-12-24

    Infusion pump software recalled over anomalies that could cause serious harm

    Fresenius Kabi USA is recalling Ivenix Infusion System LVP software versions 5.10.1 and earlier, which the firm states contain anomalies with the potential to cause serious patient harm or death.

    Product
    Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Software for the controlled administration of fluids to patients.
    Category
    Medical Device
    Distribution
    20 states
  • CriticalFDA (Devices)·Z-0914-2026·2025-12-24

    Carestation 750 anesthesia systems recalled over potential unexpected shutdown

    GE Medical Systems is recalling 888 Carestation 750 series anesthesia systems over potential unexpected shutdown if AC mains power is unplugged or fails. The action is Class I.

    Product
    GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 750 A1, REF 1012-9750-000; Carestation 750 A2, REF 1012-9750-002; Carestation 750c A1, REF 1012-9755-000; Products for which affected PMB can be used as a spare part…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0325-2026·2025-12-24

    Organic senna leaves recalled over potential contamination with Salmonella

    The Whole Herb Company is recalling 3,580 lbs of organic cut and sifted senna leaves over potential Salmonella contamination. The FDA has classified the action as Class I.

    Product
    SENNA LEAVES F/C OG Item No: SEN15001 Net Wt: 44.75 Lbs Distributed By Whole Herb Company 19800 8th Street East, Sonoma, CA 95476 UPC 10031 44312
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-0288-2026·2025-12-17

    Frozen amla slices recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen amla slices after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Amla Slices KEEP FROZEN Net Wt. 10 oz. (283 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0293-2026·2025-12-17

    Frozen aviyal mix recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen aviyal mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Aviyal Mix KEEP FROZEN Net Wt. 14.1 oz. (400 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0317-2026·2025-12-17

    White peaches in two pound bags recalled over potential Listeria contamination

    Moonlight Packing is recalling 104 cases of 2 lb bagged white peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.

    Product
    UPC 8 10248 03186 1 WHITE PEACHES CALIFORNIA FRUIT PRODUCE OF U.S.A. NET WT. 2 LBS. (907G) MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0267-2026·2025-12-17

    Frozen val papdi recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen val papdi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Select Val Papdi Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0283-2026·2025-12-17

    Frozen arvi recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen arvi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Green Peas KEEP FROZEN a) Net Wt. 3.85 LB. (1.75 kg); b) Net Wt. 2 LB. (907 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0272-2026·2025-12-17

    Frozen green chili cubes recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen green chili cubes after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Indian Kitchen Quick Cubes Ready For Cooking Green Chili of India Net Wt. 10 oz. (283 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0277-2026·2025-12-17

    Frozen cooked dum aloo recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen dum aloo after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Dum Aloo (Cooked) Net Wt. 12 oz. (340 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0264-2026·2025-12-17

    Frozen ginger garlic cubes recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen ginger garlic cubes after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Indian Kitchen Quick Cubes Ready for Cooking Ginger Garlic of India Net Wt. 10 oz. (283 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0904-2026·2025-12-17

    Frozen mixed vegetables recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen mixed vegetables after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-0259-2026·2025-12-17

    Frozen sliced violet Indian yams recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen ratalu sliced violet Indian yams after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Premium Select Ratalu Sliced Violet Indian Yams KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0285-2026·2025-12-17

    Frozen sweet corn recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen sweet corn after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Sweet Corn KEEP FROZEN Net Wt. 2 LB (907 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0248-2026·2025-12-17

    Mild cheddar cheese recalled over possible Listeria monocytogenes contamination

    Boss Dairy Farms is recalling 420 units of Charlevoix Cheese Company Mild Cheddar Cheese over possible Listeria monocytogenes contamination. The FDA has classified the action as Class I.

    Product
    Charlevoix Cheese Company Mild Cheddar Cheese, Net Wt. 8 oz (227g). UPC 8 50056-64205 7. 12 retail units per wholesale case.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-0294-2026·2025-12-17

    Frozen green garlic recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen green garlic after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Green Garlic KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0260-2026·2025-12-17

    Frozen tuvar lilva, 24 ounce bags, recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen tuvar lilva after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Premium Select Tuvar Lilva Net Wt. 1 LB 8 oz. (24 oz.) (680 g) KEEP FROZEN
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0301-2026·2025-12-17

    Frozen garlic quick cubes recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen garlic quick cubes after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Indian Kitchen Quick Cubes READY FOR COOKING Garlic of India KEEP FROZEN Net Wt. 10 oz. (283 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0291-2026·2025-12-17

    Frozen diced bottle gourd recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen diced bottle gourd after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand PREMIUM Select Dudhi (Lauki) Diced Bottle Gourd KEEP FROZEN Net Wt. 12 oz. (340 g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·H-0270-2026·2025-12-17

    Frozen cut okra recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen bhindi cut okra after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Deep-brand Select Bhindi Cut Okra KEEP FROZEN a) Net Wt. 12 oz (340 g); b) Net Wt. 1 LB 8 oz. (24 oz.) (680 g); c) Net Wt. 2 LB (907 g)
    Category
    Food
    Distribution
    0 states