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 deaths or serious injuries are reported, 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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20826–20850 of 27460

  • HighFDA (Drugs)·D-0013-2023·2022-10-26

    Acyclovir Sodium Injectable Recalled for Particulate Matter

    AuroMedics Pharma is recalling Acyclovir Sodium injection due to dark red, brown, and black particulate matter found in vials. Approximately 89,400 vials were distributed nationwide.

    Product
    ACYCLOVIR SODIUM — ACYCLOVIR SODIUM (ACYCLOVIR SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V807000·2022-10-26

    Volkswagen Atlas and Cross Sport trailing arm bolt defect recall

    Volkswagen is recalling certain 2022 Atlas and 2022-2023 Cross Sport vehicles because driver-side rear trailing arm bolts may loosen and fall out, risking loss of vehicle control.

    Product
    VOLKSWAGEN — 2022 VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0097-2023·2022-10-26

    Medical Device Recall: Roche cobas 5800 False Results Due to Baseline Anomalies

    Roche Molecular Systems recalls the cobas 5800 PCR testing instrument due to false positive and invalid results caused by anomalous baselines. This may lead to erroneous or delayed diagnoses.

    Product
    cobas 5800 instrument, Material No. 08707464001. Used for automated Polymerase Chain Reaction (PCR) based Nucleic Acid Testing (NAT) in laboratory settings.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0053-2023·2022-10-26

    Lyons Ready Care Thickened Orange Nectar Recalled for Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Orange Nectar due to indication of product spoilage. The recall affects 1,272 cases distributed nationwide with specific lot numbers and best-by dates in March 2023.

    Product
    Lyons Ready Care Thickened Orange Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Devices)·Z-0105-2023·2022-10-26

    Medical device assay may report falsely elevated lithium levels

    Siemens' Atellica CH Lithium diagnostic assay may falsely report elevated lithium levels, potentially leading to incorrect dose adjustments in patients on lithium therapy.

    Product
    Atellica CH Lithium (Li), Siemens Material Number 11097535. in vitro diagnostic assay
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0051-2023·2022-10-26

    Tuscan Garden Italian Dressing Recalled for Undeclared Soy and Wheat Allergens

    Tuscan Garden Restaurant Style Italian Dressing is being recalled due to undeclared soy and wheat allergens. The recall affects 26,370 mixed cases distributed across 20 states.

    Product
    Tuscan Garden Restaurant Style Italian Dressing , Net 16 FL OZ (1 PT) 473 mL, Plastic Bottle 12 count mixed case containing 3 Dressing flavors, including 8 bottles of the Restaurant Style Italian
    Category
    Food
    Distribution
    19 states
  • HighNHTSA·22V806000·2022-10-26

    Multiple 2021-2022 Audi models recalled for rearview camera failure

    Volkswagen Group of America is recalling certain 2021-2022 Audi vehicles. The infotainment system may fail to display the rearview camera, reducing rear visibility and increasing crash risk.

    Product
    AUDI — 2022 AUDI Q8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0063-2023·2022-10-26

    Lyons Ready Care Thickened Orange Juice recalled for spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Orange Juice 46 fl oz cartons due to indication of product spoilage. Specific lot numbers distributed nationwide are affected.

    Product
    Lyons Ready Care Thickened Orange Juice packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Food)·F-0054-2023·2022-10-26

    Lyons Ready Care Thickened Apple Honey Nectar Recalled Due to Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Apple Honey Nectar due to indications of product spoilage. The nationwide recall affects 645 cases with specific lot numbers and best-by dates in March 2023.

    Product
    Lyons Ready Care Thickened Apple Honey Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Devices)·Z-0117-2023·2022-10-26

    MitraClip G4 and TriClip G4 Cardiac Devices Recalled for Clip Locking Malfunction

    Abbott has recalled MitraClip G4 and TriClip G4 cardiac repair devices due to clip locking malfunctions that may prevent proper device deployment. These malfunctions could lead to failed procedures and serious complications including device embolization.

    Product
    Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT, MitraClip G4 CDS NTW REPAIR-MR Clinical/CDS0704-NTW, MitraClip G4 CDS XT REPAIR-MR Clinical/CDS0704-XT, MitraClip G4 CDS XTW REPAIR-MR Clinical/CDS0704-XTW, TriClip NT Clip Delivery Sys CLIN/TCDS0203-NT, TriCli
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0043-2023·2022-10-26

    Market Pantry White Fudge Animal Cookies Recalled for Metal Contamination

    Market Pantry White Fudge Animal Cookies sold at Target may contain metal fragments. D. F. Stauffer Biscuit Co is recalling 883 cases distributed nationwide.

    Product
    White frosted animal cookies with multi-colored non-pareils in a 44oz plastic jug labeled "Market Pantry White Fudge Animal Cookies"
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0115-2023·2022-10-26

    MitraClip Clip Delivery System Recalled for Locking Malfunctions

    Abbott Vascular is recalling MitraClip Clip Delivery System devices due to observed increases in clip locking malfunctions that can lead to recurrence of mitral regurgitation, device embolization, or tissue injury.

    Product
    Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT, MitraClip G4 Clip Delivery System NTW US/CDS0701-NTW, MitraClip G4 Clip Delivery System XT US/CDS0701-XT, MitraClip G4 Clip Delivery System XTW US/CDS0701-XTW.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0113-2023·2022-10-26

    Reusable Oral Syringe Recalled for Unapproved Plunger Material

    Medicina UK Ltd is recalling Reusable Oral Syringes because plungers were manufactured from unapproved polyethylene instead of the specified polypropylene material.

    Product
    Medicina Reusable Oral syringe 5ml Code: OTH05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0062-2023·2022-10-26

    Lyons Ready Care Thickened Apple Juice Recalled for Spoilage Indication

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Apple Juice due to indication of product spoilage. The recall affects 320 cases distributed nationwide.

    Product
    Lyons Ready Care Thickened Apple Juice packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Drugs)·D-0015-2023·2022-10-26

    Saline Solution Injection Recalled Nationwide Due to Sterility and Leakage

    Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection distributed nationwide due to lack of assurance of sterility and potential leakage. Multiple lot numbers with expiration dates ranging from May 2023 to August 2023 are affected.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0101-2023·2022-10-26

    DePuy Synthes Hammertoe Implants Recalled for Incorrect Drill Guide Size

    Synthes (USA) Products LLC is recalling 196 DePuy Synthes Hammertoe Continuous Compression Implants due to an incorrect drill guide size that will not properly prepare bone for the implant, creating potential for bone damage.

    Product
    DePuy Synthes Hammertoe Continuous Compression Implants, Product No. 46.239.001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0110-2023·2022-10-26

    Oral Tip Syringes Recalled Due to Unapproved Plunger Material

    Medicina Oral Tip Syringes are being recalled because the plunger component was made with polyethylene instead of the approved polypropylene material. No illnesses or injuries have been reported.

    Product
    Medicina Oral Tip Syringe 1ml Code: OT01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0047-2023·2022-10-26

    Trader Joe's Organic Tortilla Chip Rounds recalled for undeclared milk and soy

    Trader Joe's Organic Yellow Tortilla Chip Rounds may contain undeclared milk and soy allergens. The product contains small amounts of Spicy Cheese Crunchies which were not listed on the label.

    Product
    16 oz. bags of Trader Joe's Organic Yellow Tortilla Chip Rounds. UPC: 0074-0449 Distributed and Sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and Sold Exclusively By: Trader Joe's, Monro
    Category
    Food
    Distribution
    16 states
  • HighFDA (Drugs)·D-0011-2023·2022-10-26

    Rifampin Capsules recalled due to excessive impurity levels

    Golden State Medical Supply Inc. is recalling Rifampin Capsules, USP, 300 mg, because samples exceeded acceptable limits for 1-Methyl-4-Nitrosopoperazine (MNP), an impurity. Multiple lot numbers were distributed nationwide.

    Product
    Rifampin Capsules, USP, 300 mg, packaged in a) 30-count bottle (NDC 51407-323-30), b) 60-count bottle (NDC 51407-323-60), c) 100-count bottle (NDC 51407-323-01), Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0095-2023·2022-10-26

    BD Vacutainer Blood Alcohol Testing Tubes Recalled for Analytical Interference

    BD Vacutainer blood collection tubes are recalled due to isobutylene contamination that may cause false positive results in blood alcohol testing.

    Product
    BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting, separating, and processing blood for blood alcohol determination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0096-2023·2022-10-26

    Laryngeal mask airway recalled for incorrect size marking

    Intersurgical Solus Standard size 3 laryngeal mask airways are marked with incorrect size 4 information, which may cause misuse or improper sizing of the airway device.

    Product
    Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-0069-2023·2022-10-26

    Tastykake Glazed Cherry Pie Recalled Due to Undeclared Soy Lecithin

    Flowers Foods is recalling Tastykake Glazed Cherry Pie due to undeclared soy lecithin in the product. The recalled product may pose a health risk to consumers with soy allergies.

    Product
    TASTYKAKE GLAZED CHERRY PIE NET WT 4.5 OZ (128g) UPC 0 25600 00969 7 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-0094-2023·2022-10-26

    N Antiserum to Human IgG Fails High-Dose Hook Effect Performance Standards

    Siemens N Antiserum to Human IgG reagent batches are not meeting performance standards for high-dose immunoassay testing. The issue affects 10,201 packs distributed nationwide and may result in inaccurate diagnostic test results.

    Product
    N Antiserum to Human IgG, 5mL Variant for BN II System and BN ProSpec System- IVD Siemens Material Number (SMN): 10446299
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0044-2023·2022-10-26

    Cheese Straws Recalled for Undeclared Wheat and Milk Allergens

    Flathau's Fine Foods is recalling Cheese Straws Delta Bred products due to undeclared wheat and milk allergens. 433 units were distributed across 12 states. Consumers with allergies should stop consuming and discard affected products.

    Product
    Flathau's Fine Foods Cheese Straws Delta Bred Cheese Straws packaged in 4oz and 6oz cartons 12 packages per case
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-0048-2023·2022-10-26

    Seeking Health Optimal Multivitamin Chewable Supplement Recalled for Excess Copper

    Seeking Health LLC is recalling Optimal Multivitamin Chewable Dietary Supplement tablets because lab testing found higher copper levels than stated on the label.

    Product
    Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product is packaged in white non-flex plastic bottles. UPC: 810007520902. Product labels read in part: Adults and children age 4 and over; Chew 2 tablets daily. Servi
    Category
    Consumer Product
    Distribution
    51 states