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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8751–8775 of 114917

  • HighFDA (Drugs)·D-0560-2025·2025-08-13

    Compounded tirzepatide 16.6 mg vials recalled over lack of processing controls

    Tirzepatide + Niacinamide 16.6 mg + 1.0 mg/0.5 mL injection solution compounded by Aequita Pharmacy is being recalled for lack of processing controls. 155 vials are affected.

    Product
    Tirzepatide + Niacinamide 16.6 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 3 x 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034.
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·H-0389-2025·2025-08-13

    Breaded jalapeno mac and cheese bites used a recalled Listeria ingredient

    Breaded Jalapeno Mac & Cheese Bites in 30 lb cases are being recalled because a supplier recalled an ingredient used in the finished product for possible Listeria monocytogenes contamination. 819 cases affected.

    Product
    BREADED JALAPENO MAC & CHEESE BITES Mac & Cheese Bites, Net Wt. 30 LB. 90935, (01)10077886909359, Prepared and Packaged by LOUISA FOOD PRODUCTS, INC. St. Louis, MO 63136; COOKING DIRECTIONS: Deep fry at 350F for 3 1/2 to 4 minutes or until internal temperature reaches 160F.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0559-2025·2025-08-13

    Compounded tirzepatide 13.2 mg vials recalled over lack of processing controls

    Tirzepatide + Niacinamide 13.2 mg + 1.0 mg/0.5 mL injection solution compounded by Aequita Pharmacy is being recalled for lack of processing controls. 143 vials are affected.

    Product
    Tirzepatide + Niacinamide 13.2 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034.
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-2275-2025·2025-08-13

    Size 2 Guedel airways may carry small burrs that could detach

    One-piece Guedel airways, size 2, are being recalled because of potential contamination with small burrs which, if they detach, could be inhaled. 2,800 pieces are affected.

    Product
    One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Drugs)·D-0574-2025·2025-08-13

    Spironolactone 25 mg tablets recalled after aluminum was found in product

    Spironolactone Tablets USP 25 mg are being recalled because of the presence of a foreign substance identified as aluminum. 11,328 bottles are affected.

    Product
    SPIRONOLACTONE — SPIRONOLACTONE (SPIRONOLACTONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0392-2025·2025-08-13

    Cesarina Mediterranean mix cookies omit sesame from the contains statement

    Cesarina Mediterranean Mix Cookies, 16 oz, are being recalled because sesame is not listed in the Contains statement. 30 cases are affected.

    Product
    MEDITERRANEAN MIX COOKIES, Cesarina Cookies, Net Weight. 16 oz. (454g), packaged in plastic clam shell containers, 12 packages per master case. Dry storage.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0563-2025·2025-08-13

    Compounded semaglutide 1.5 mg vials recalled over lack of processing controls

    Semaglutide + Cyanocobalamin 1.5 mg + 0.25 mg/0.5 mL injection solution compounded by Aequita Pharmacy is being recalled for lack of processing controls. 190 vials are affected.

    Product
    Semaglutide +Cyanocobalamin 1.5 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034.
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0567-2025·2025-08-13

    Duloxetine delayed-release capsules exceed the interim nitrosamine impurity limit

    Duloxetine Delayed-Release 20 mg capsules packaged by Direct Rx are being recalled because a nitrosamine drug substance related impurity was present above the proposed interim limit. 16 bottles affected.

    Product
    Duloxetine D/R, 20 mg, 30 Caps, 30-count bottle, RX Only, Packaged & Distributed by: Direct Rx, Dist. By Breckenridge Pharm., Inc., Berlin, CT 06037, NDC 61919-422-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0385-2025·2025-08-13

    Favorite Day frosted sugar cookies may contain wood foreign material

    Favorite Day Bakery Frosted Sugar Cookies, 10 count, are being recalled because of foreign material, specifically wood. 803 cases are affected.

    Product
    Favorite Day Bakery Frosted Sugar Cookies, 10 count, Net Wt 13.5 oz (383g). UPC - 85239-41250 3. Dist. By Target Corporation, Minneapolis, MN 55403. Product of Canada.
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Food)·H-0417-2025·2025-08-13

    Yoplait Harvest Peach yogurt recalled after a shipping trailer temperature excursion

    Yoplait Original Harvest Peach Yogurt, 6 oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Yoplait Original Harvest Peach Yogurt, 6 OZ (170g), packaged in a plastic cup, UPC: 170470003075
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2258-2025·2025-08-13

    Major thoracoscopy basins contain an inadvertently resterilized visualization system

    Major Thoracoscopy Basin medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 128 units are affected.

    Product
    MAJOR THORACOSCOPY BASIN. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0413-2025·2025-08-13

    Silk vanilla almondmilk recalled after a shipping trailer temperature excursion

    Silk Vanilla AlmondMilk, 64 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Silk Vanilla AlmondMilk, 64 FL OZ (2 QT) 1.89 L, packaged in a paper carton, UPC: 025293000995
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2250-2025·2025-08-13

    GYN laparoscopy packs contain an inadvertently resterilized visualization system

    GYN Laparoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 346 units are affected.

    Product
    GYN LAPAROSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2271-2025·2025-08-13

    DxI 600 with Spot B analyzer motor current resets below requirement

    DxI 600 Access Immunoassay Analyzers with Spot B are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors. 177 systems are affected.

    Product
    DxI 600 Access Immunoassay Analyzer W/Spot B, Part Number A71460
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2263-2025·2025-08-13

    Robotic uro/gyn packs contain an inadvertently resterilized visualization system

    Robotic Uro/Gyn Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 372 units are affected.

    Product
    ROBOTIC URO/GYN PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Drugs)·D-0571-2025·2025-08-13

    Xolair auto-injectors exposed to temperatures outside labeled storage requirements

    Xolair (omalizumab injection) 150 mg/mL auto-injectors are being recalled because of CGMP deviations: the product was exposed to temperatures outside its labeled storage requirements. 6 units affected.

    Product
    XOLAIR — XOLAIR (OMALIZUMAB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2243-2025·2025-08-13

    daVinci urology and prostate packs contain a resterilized visualization system

    DA VINCI PACK URO/PROSTATE medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 21 units affected.

    Product
    DA VINCI PACK URO/PROSTATE. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2238-2025·2025-08-13

    BD Trucount control kits carry incorrect standard deviation values for beads

    BD Trucount Controls 30 Test kits are being recalled because they contain incorrect standard deviation values for the low and high control beads, which compromises accurate bead count calculation. 629 kits affected.

    Product
    BD Trucount Controls, 30 Test - REF: 340335
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0404-2025·2025-08-13

    Imperial vegetable oil spread recalled after a shipping trailer temperature excursion

    Imperial 48% Vegetable Oil Spread Margarine Sticks are being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 8 units are affected.

    Product
    Imperial 48% Vegetable Oil Spread Margarine Sticks, NET WT 16 OZ (1 LB) 453g, packaged in a cardboard box, UPC: 011115871324
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2259-2025·2025-08-13

    General robotic packs contain an inadvertently resterilized visualization system

    PACK GENERAL ROBOTIC medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 656 units are affected.

    Product
    PACK GENERAL ROBOTIC. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0407-2025·2025-08-13

    Milo's famous sweet tea recalled after a shipping trailer temperature excursion

    Milo's Famous Sweet Tea, 1 gallon, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units are affected.

    Product
    Milo's Famous Sweet Tea, 128 FL OZ (1 GAL) 3.78 L, packaged in a plastic jug, UPC: 091475511009
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0416-2025·2025-08-13

    Velveeta sharp cheddar slices recalled after a shipping trailer temperature excursion

    Velveeta Slices Sharp Cheddar, 16 count, are being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Velveeta Slices Sharp Cheddar, 16 ct., NET WT 12 OZ (340g), packaged in plastic/cardboard, UPC: 021000044894
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2252-2025·2025-08-13

    HVI cardiac robot packs contain an inadvertently resterilized visualization system

    HVI Cardiac Robot Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 20 units are affected.

    Product
    HVI CARDIAC ROBOT PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2249-2025·2025-08-13

    GS endoscopy packs contain an inadvertently resterilized visualization system

    GS Endoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 816 units are affected.

    Product
    GS ENDOSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states