The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mis labeling recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

5726–5750 of 9610

  • HighFDA (Devices)·Z-1573-2016·2016-05-04

    Philips NeuViz 16 CT Scanner Recall for Patient Data Error

    Philips and Neusoft are recalling 37 NeuViz 16 CT scanners due to a software defect that may allow previous patient images to be pasted into the current patient's record.

    Product
    NeuViz 16 Multi-Slice CT Scanner System PN: 989605858501 a whole body computed tomography X-ray system featuring a continuously rotating X-ray tube and detector array with multi-slice capability up to 16 slices simultaneously.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-1563-2016·2016-05-04

    3M Steri-Vac Gas Sterilizer Valves Recalled for Labeling Error

    3M is recalling 74 Steri-Vac Gas Sterilizer valves due to a labeling error that could cause incorrect installation and potential valve failure.

    Product
    3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL.
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Food)·F-1129-2016·2016-05-04

    NOW Foods Andrographis Extract Recalled for Undeclared Soy Lecithin

    NOW Foods is recalling Andrographis extract 400 mg capsules due to undeclared soy lecithin. The product was distributed to 499 consignees in the US and one in Japan.

    Product
    Andrographis extract 400 mg packaged in a white and orange bottle containing 90 capsules. The bottle has a blue cap and white lettering.
    Category
    Food
    Distribution
    49 states
  • HighFDA (Food)·F-1131-2016·2016-05-04

    NOW Foods Recalls Gingko Biloba Supplements Due to Undeclared Soy

    NOW Foods is recalling Gingko Biloba 60mg capsules because they contain undeclared soy lecithin. Consumers should stop using the product and return it to the place of purchase.

    Product
    Gingko Biloba 60mg packaged in a white and orange bottle containing 120 capsules. The bottle has a blue cap and white lettering.
    Category
    Food
    Distribution
    49 states
  • HighFDA (Food)·F-1248-2016·2016-05-04

    Duncan Hines Swiss Chocolate Cake Mix Recalled for Undeclared Milk

    Pinnacle Foods is recalling Duncan Hines Swiss Chocolate Cake Mix because a natural flavoring containing milk was used, but the product was labeled as non-milk.

    Product
    Duncan Hines Moist Deluxe Swiss Chocolate (Chocolate Suizo) Cake Mix, Net Wt. 16.5 oz. (1 LB 5 oz.) 468 g, Distributed by: Pinnacle Foods, Cherry Hill, New Jersey USA, UPC 6 44209 309748 7
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1247-2016·2016-05-04

    Duncan Hines Swiss Chocolate Cake Mix Recalled for Undeclared Milk

    Pinnacle Foods is recalling Duncan Hines Swiss Chocolate Cake Mix because a natural flavoring containing milk was used, but the product was labeled as non-milk.

    Product
    Duncan Hines Signature Swiss Chocolate Cake Mix, 16.5 oz. cartons, Distributed by: Pinnacle Foods, Cherry Hill, New Jersey USA, UPC 6 44209 41120 7
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1246-2016·2016-05-04

    Bissinger's Milk Chocolate Eggs Recalled for Mislabeling Artificial Vanillin as Vanilla

    Karl Bissinger, LLC is recalling Bissinger's Milk Chocolate Eggs because the product contains artificial vanillin but is labeled as containing vanilla.

    Product
    Bissinger's Milk Chocolate Eggs packaged in 6.5 oz (UPC 846107009382) Item: #11108 or 1 lb. (UPC 846107003458) Item: # 111049 plastic bags. Bissinger's Handcrafted Chocolatier, St. Louis, MO.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1565-2016·2016-05-04

    Baxter APD Cycler Recall for Incomplete Clinician Guide Instructions

    Baxter Healthcare is recalling 10 automated peritoneal dialysis cyclers because the clinician guide lacks instructions for priming the patient line.

    Product
    Automated peritoneal dialysis (APD) cycler
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1567-2016·2016-05-04

    Boston Scientific Recalls Mislabeled Ultraflex Tracheobronchial Stents

    Boston Scientific is recalling four Ultraflex Tracheobronchial stents because 10mm diameter units were mislabeled as 12mm diameter.

    Product
    Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System 12mm X 30mm Material Number: M00576550 The stent system is a permanently implanted expandable metal stent designed for palliation of tracheobronchial (TB) strictures. The system consists of a flexible d
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1582-2016·2016-05-04

    Teleflex Pleur-evac Chest Drainage System Recalled for Missing Tyvek Bag Label

    Teleflex Medical is recalling Pleur-evac Chest Drainage Systems because the Tyvek bag label is missing, preventing identification of material code, lot number, and expiration date.

    Product
    Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product Usage: Pleur-Evacs are sterile, single-use, chest drainage systems intended for post-operative use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0834-2016·2016-05-04

    SKY Aspirin Chewable Tablets Recalled for Incorrect Outer Carton Labeling

    McKesson Packaging Services is recalling SKY Aspirin Chewable Tablets because the outer cartons were incorrectly labeled. The recall addresses a labeling mix-up.

    Product
    SKY Aspirin Chewable Tablets, 81 mg, Unit Dose 750 tablets (25 x 30) box, OTC, Distributed by: McKesson Packaging Service, Concord, NC 28027, NDC 63739-434-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·16V258000·2016-04-29

    Forest River Cardinal RVs Recalled for Incorrect Tire Placard Information

    Forest River is recalling 2016-2017 Cardinal RVs because the tire placard lists incorrect tire and rim specifications, which could lead to under-inflation and tire blowouts.

    Product
    FOREST RIVER — FOREST RIVER CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1096-2016·2016-04-27

    Chicago Kimchee Recalls Kimchee for Undeclared Anchovies

    Chicago Kimchee is recalling chopped Kimchee products due to undeclared anchovies, a major food allergen.

    Product
    Korea chopped Kimchee packaged in 1 gallon, 1/2 gallon, 1/4 gallon, and 1/8 gallon packaged in glass jars inside plastic containers with multi colored label and black lettering.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1122-2016·2016-04-27

    Servatii Christmas Cookie Tray Recalled for Misleading Allergen Labeling

    Servatii Inc is recalling Christmas Cookie Trays because the labels do not accurately describe allergens, including butter, margarine, and nuts.

    Product
    SERVATii Pastry Shop & Deli 12" Christmas Cookie Tray INGREDIENTS: ***Butter, Margarine***Nuts***1.51lb(682gr) EUROPEAN SPECIALTIES Cincinnati, Ohio 45227 UPC 0 36746 03992 9
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1009-2016·2016-04-27

    True Nature Garlic Hummus Recalled for Undeclared Soy

    True Nature LLC is recalling Garlic Hummus due to undeclared soy from the ingredient Tamari. The product was sold in Oregon and Washington.

    Product
    Garlic Hummus - 9 oz container
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1090-2016·2016-04-27

    Brett Anthony Foods Recalls Wild Mushroom Soup for Undeclared Chestnuts

    Brett Anthony Foods is recalling 24 oz containers of Wild Mushroom Soup because the product is mislabeled and does not declare chestnuts.

    Product
    Wild Mushroom Soup packaged in a 24 oz clear plastic container with green and white label and green lettering.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1516-2016·2016-04-27

    Stryker GDC 360 Detachable Coils Recalled for Incorrect DFU Packaging

    Stryker Neurovascular is recalling GDC 360 Detachable Coils because an incorrect Device Form Unique (DFU) was packaged with two lots.

    Product
    GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile; Model number: M0033471020SR0; Neurology: GDC 360 Detachable Coils are intended for embolization of those intracranial aneurysms that because of their morphology, their location, or the patients general medical conditio
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1498-2016·2016-04-27

    Optovue iVue OCT Systems Recalled for Software Display Anomaly

    Optovue is recalling iVue and iVue 500 OCT systems due to a software anomaly that may display duplicate eye images instead of distinct right and left views.

    Product
    iVue and iVue 500 (now called iScan) OCT systems with software version 2016.0.0.127 (USA only) and 2016.1.0.127 (out of US) Opthalmic: iVue is a non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional and three-dimensi
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-1524-2016·2016-04-27

    Synthes Recalls Cervical Spine Screws Due to Lot Swapping Error

    Synthes (USA) Products LLC is voluntarily recalling specific lots of cervical spine screws because two different screw types were swapped during manufacturing.

    Product
    Cervical Spine Locking Plate (CSLP) System, 4mm Cancellous Self Tapping Screw, Length 16mm Lot # 9666776 and 4mm Cortex Standard Screw, Length 16mm Lot # 9671879
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1523-2016·2016-04-27

    Biocare Medical Recalls Mislabeled Mach 4 Mouse Probe Vials

    Biocare Medical is recalling a single lot of Mach 4 Mouse Probe vials that may be mislabeled as HRP-Polymer.

    Product
    Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit; Catalog number M4U534L; For In Vitro Use Immunology: MACH 4 Universal HRP-Polymer is a horseradish peroxidase (HRP)-antibody conjugate system intended for use in the detection of mouse lgG and lgM, and rabb
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·16T006000·2016-04-27

    Pirelli Recalls Tires Missing Required Date Codes

    Pirelli is recalling specific P Zero Trofeo tires that may lack required date codes, which could hinder identification during safety issues.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1501-2016·2016-04-27

    Medtronic Recalls CareLink iPro2 Reports Due to Time Zone Error

    Medtronic MiniMed is recalling 19 CareLink iPro Therapy Management reports because they used the wrong time zone, causing inaccurate timestamps for continuous glucose data.

    Product
    CareLink iPro2 Reports, Model No. MMT-7340 is software intended to retrospectively calibrates sensor data and provides reports of continuous glucose information
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-1509-2016·2016-04-27

    OraSure Recalls OraQuick HCV Visual Reference Panel Due to Incorrect Insert

    OraSure Technologies is recalling 244 OraQuick HCV Visual Reference Panel kits because the package insert may be incorrect, potentially containing instructions for a different test.

    Product
    OraQuick HCV Visual Reference Panel Intended to assist new operation in becoming proficient at reading specimens with antibody levels near the limit of detection of the device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowNHTSA·16V237000·2016-04-22

    Forest River Recalls Prime Time Crusader Trailers for Incorrect Federal Placard

    Forest River is recalling 2015-2017 Prime Time Crusader trailers because the Federal Placard incorrectly lists the Cargo Carrying Capacity. Dealers will install corrected placards free of charge.

    Product
    PRIME TIME — PRIME TIME CRUSADER
    Category
    Vehicle
    Distribution
    Distributed nationwide