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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13876–13900 of 36679

  • CriticalFDA (Food)·F-1486-2019·2019-06-26

    Bobbie Milk-Based Powder Companion Formula Recalled for Inadequate Infant Nutrition

    Bobbie Baby is recalling specific lots of Milk-Based Powder Companion Formula because the product does not provide adequate nutrition for some infants.

    Product
    Bobbie Milk-Based Powder Companion Formula Net Wt. 14.1 oz. (400g) 22 servings per container Serving Size 4 scoops. Made in Germany Distributed by Bobbie Baby 520 Divisadero ST # 111 San Francisco, CA 94117
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1529-2019·2019-06-26

    Mothers' Milk Bank at Austin Recalls Pasteurized Donor Human Breast Milk

    Mothers' Milk Bank at Austin is recalling 54 bottles of pasteurized donor human breast milk due to a positive microbiological culture for Bacillus cereus.

    Product
    Pasteurized donor human breast milk, Pool 9029, Batch 1 packaged in 3 ounce (90 cc) plastic bottles
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1786-2019·2019-06-26

    Monarch EndoTool IV Software Recalled for High Insulin Dosing Calculations

    Monarch Medical Technologies is recalling EndoTool IV software versions 1.8 through 1.10 because insulin dosing calculations were erroneously high.

    Product
    Monarch Medical Technologies EndoTool IV, Versions 1.8, Version 1.8.5 and higher, and Version 1.9 and Version 1.10.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1750-2019·2019-06-26

    GE Healthcare Recalls Discovery ML DR PET/CT Systems Due to Table Stop Defect

    GE Healthcare is recalling 1,113 Discovery ML DR PET/CT systems because the table may stop moving without stopping X-ray exposure.

    Product
    Discovery Ml DR Product Usage: The systems are intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging and localization of emission activity in patient anatomy by means of integrated PET and CT images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1749-2019·2019-06-26

    GE Healthcare Recalls Discovery ML PET/CT Systems Due to X-Ray Safety Defect

    GE Healthcare is recalling 1,113 Discovery ML PET/CT systems because the table may stop moving without stopping X-ray exposure.

    Product
    Discovery Ml Product Usage: The systems are intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging and localization of emission activity in patient anatomy by means of integrated PET and CT images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1478-2019·2019-06-26

    APS BioGroup Recalls Immuno PRP Spray Due to Bacterial Contamination

    APS BioGroup is recalling Immuno PRP Spray because testing found elevated levels of Stenotrophomonas maltophilia. The product was distributed nationwide and in Switzerland.

    Product
    Immuno PRP Spray, UPC 8 12527 01176 2. Colostrum Polypeptides. 5 fl oz (140 mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1480-2019·2019-06-26

    APS BioGroup Recalls DPS Throat Spray Due to Bacterial Contamination

    APS BioGroup is recalling DPS Throat Spray because testing found elevated levels of Stenotrophomonas maltophilia bacteria.

    Product
    DPS Throat Spray, UPC 8 55602 00021 3. Colostrum Immune Concentrate. Net 150 ml
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1829-2019·2019-06-26

    Covidien EGIA 60 Articulating Medical Stapler Recall for Missing Pins

    FDA is recalling 3,113,280 units of the EGIA 60 Articulating Medical Stapler due to missing pin components that may cause incomplete staple formation and serious surgical complications.

    Product
    EGIA 60 ARTICULATING MED THICK SULU , EGIA60AMT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1408-2019·2019-06-26

    P & L Developments Recalls Cetirizine Oral Solution Due to Bacterial Contamination

    P & L Developments, LLC is recalling 17,664 bottles of Cetirizine Oral Solution due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.

    Product
    Cetirizine Oral Solution 1 mg/mL, Children's Allergy, Antihistamine, Dye Free, Grape Flavor, 4 FL. oz. Bottle, Distributed by C.D.M.A. Inc., Novi, MI 48376, Quality Choice, NDC 63868-430-04, UPC 635515992474.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1832-2019·2019-06-26

    Recall of Signia Tri-Staple 2.0 Surgical Reloads Due to Missing Pins

    Covidien LLC is recalling Signia Tri-Staple 2.0 reloads because missing pin components may cause incomplete staple formation, potentially leading to serious surgical complications.

    Product
    SIGNIA TRI-STAPLE 2.0 30MM MEDIUM/ THICK RELOAD , SIG30AMT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1443-2019·2019-06-26

    Zydus Recalls Pramipexole Dihydrochloride Tablets Due to Cross-Contamination

    Zydus Pharmaceuticals USA Inc. is recalling Pramipexole Dihydrochloride Tablets 0.125 mg due to cross-contamination caused by cleaning failures.

    Product
    Pramipexole DihydrochlorideTablets 0.125 mg, 90-count bottle, Rx Only, Manufactured by: Cadila Healthcare Ltd Ahmedabad, India. Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534. NDC 68382-196-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1490-2019·2019-06-26

    Whole Foods Sun-Dried Tomato Pesto Recalled for Undeclared Allergens

    Whole Foods Market is recalling sun-dried tomato pesto because the labels failed to declare milk, walnuts, and pine nuts.

    Product
    Sun-dried tomato pesto, sold by weight in plastic deli containers PLU code beginning with 256009
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-1409-2019·2019-06-26

    P & L Developments Recalls Cetirizine Oral Solution Due to Bacterial Contamination

    P & L Developments is recalling 124,512 bottles of Up & Up Children's Cetirizine Oral Solution due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.

    Product
    Cetirizine Oral Solution 1 mg/mL, Up & Up, Children's allergy relief, Antihistamine, Dye Free, Grape Flavor, 4 FL. oz. (118 mL) Bottle, Distributed by Target Corporation, Minneapolis, MN 55403, NDC 11673-178-04, UPC 359726178044.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1440-2019·2019-06-26

    Zydus Recalls Anastrozole Tablets Due to Cross-Contamination

    Zydus Pharmaceuticals is recalling Anastrozole tablets due to cross-contamination from cleaning failures. The recall covers 1.4 million bottles distributed nationwide.

    Product
    ANASTROZOLE — ANASTROZOLE (ANASTROZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1472-2019·2019-06-26

    Renaissance Food Group Recalls 365 by Whole Foods Yellowfin Tuna Salad

    Renaissance Food Group LLC is recalling 365 by Whole Foods Yellowfin Tuna Salad due to undeclared soy. The recall covers 144 units sold in Texas, Louisiana, and Oklahoma.

    Product
    365 by Whole Foods Yellowfin Tuna Salad packaged in a clear plastic clamshell 8 Oz. UPC 81641602120
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1833-2019·2019-06-26

    Recall of Signia Tri-Staple 2.0 Reloads Due to Missing Pin Components

    Covidien LLC is recalling Signia Tri-Staple 2.0 reloads because missing pin components may cause incomplete staple formation, leading to serious surgical complications.

    Product
    SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA, SIG45AXT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1828-2019·2019-06-26

    FDA Recalls Covidien EGIA 60 Articulating Extra Thick Sulu Devices

    The FDA is recalling 3,113,280 units of the EGIA 60 Articulating Extra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious surgical complications.

    Product
    EGIA 60 ARTICULATING EXTRA THICK SULU, Item code EGIA60AXT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1826-2019·2019-06-26

    Covidien EGIA 45 Articulating Medical Stapler Recall for Missing Pins

    FDA is recalling 3.1 million EGIA 45 staplers due to missing pins that may cause incomplete stapling and serious surgical complications.

    Product
    EGIA 45 ARTICULATING MED THICK SULU, Item Code EGIA45AMT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1836-2019·2019-06-26

    Signia Tri-Staple Surgical Device Recalled Due to Missing Pin Components

    The FDA is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, leading to serious surgical complications.

    Product
    SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC , SIG60CTAMT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1835-2019·2019-06-26

    Recall of Signia Tri-Staple Surgical Devices Due to Missing Pin Components

    Covidien LLC is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, potentially leading to serious surgical complications.

    Product
    SIGNIA TRI-STAPLE 2.0 CURVED TIP 45MM MEDIUM/ THIC , SIG45CTAMT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1469-2019·2019-06-26

    Renaissance Food Group Recalls Tuna Salad Wraps for Undeclared Soy

    Renaissance Food Group is recalling 365 by Whole Foods Market Classic Tuna Salad Wraps due to undeclared soy. The recall covers 84 units sold in Texas, Louisiana, and Oklahoma.

    Product
    365 by Whole Foods Market Classic Tuna Salad Wrap packaged in a clear cellophane 7.75 Oz. UPC 81641602250
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·19V493000·2019-06-26

    Subaru Recalls 2019 Legacy and Outback for Body Strength Defect

    Subaru is recalling 2019 Legacy and Outback vehicles because improperly applied spot welds may reduce body strength, increasing injury risk in a crash.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide