The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 mis labeling recalls we have scored against our rubric, 160 (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.

1976–2000 of 9607

  • ModerateFDA (Drugs)·D-1362-2020·2020-07-08

    Children's Dimetapp Cold & Cough Recalled for Missing Dosing Cup Graduations

    Glaxosmithkline is recalling Children's Dimetapp Cold & Cough bottles because the included dosing cups are missing graduation marks for certain age groups.

    Product
    Childrens Dimetapp Cold & Cough, For ages 6 yrs. & over, 8 FL OZ. bottle, (237 mL), Distributed by: Pfizer Madison, NJ 07940, Made in Canada, UPC: 60300312234196, NDC: 0031-2234-19.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2478-2020·2020-07-08

    Ortho Organizers Recalls Mislabeled Maestro Orthodontic Brackets

    Ortho Organizers is recalling Maestro Orthodontic Brackets due to mislabeling. The recall involves 147 kits distributed to US and international consignees.

    Product
    Maestro Orthodontic Bracket REF711-298Q QTY. 20 Rx Only (01)00190707017064 (10)889437 (422)484 Maestro Orthodontic Bracket REF711-299MCQ QTY. 20 Rx Only (01)00190707017071(10)889437 (422)484
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2466-2020·2020-07-08

    ROi CPS LLC Recalls Respirator Crash Cart Kits Due to Labeling Error

    ROi CPS LLC is recalling 200 Respirator Crash Cart Kits because the kits are labeled with an expiration date later than the soonest component to expire.

    Product
    Respirator Crash Cart Kit
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2427-2020·2020-07-01

    Argon Medical Devices Recalls BioPince Biopsy Instruments Due to Labeling Error

    Argon Medical Devices is recalling BioPince Full Core Biopsy Instruments because of incorrect product labeling. The recall affects 165 units in the U.S. and 330 units internationally.

    Product
    BioPince Full Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY.: 5/CS - Product Usage: The disposable, automatic BioPince Full Core Biopsy Instrument is used to obtain multiple core samples from soft tissue such as liver, kidney, abdominal ma
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1341-2020·2020-07-01

    Alembic Recalls Aripiprazole Tablets Due to Labeling Error

    Alembic Pharmaceuticals is recalling aripiprazole tablets because bottles labeled as 2 mg contained 5 mg tablets. The error affects 19,153 bottles distributed nationwide.

    Product
    ARIPIPRAZOLE — ARIPIPRAZOLE (ARIPIPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2407-2020·2020-07-01

    Utak Trace Elements Serum Control Recalled for Incorrect Reference Values

    Utak Laboratories is recalling 1,395 vials of NR Trace Elements Serum Control due to incorrect cadmium reference values and expected ranges.

    Product
    Utak NR Trace Elements Serum Control, 5 ml, REF 66816. The responsible firm on the label is UTAK LABORATORIES, INC., Valencia, CA. Control for in vitro diagnostics.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1372-2020·2020-07-01

    Nabumetone Tablets Recalled for Missing Medication Guide Labeling

    American Health Packaging is recalling 265 cartons of Nabumetone Tablets because the carton label did not include the required statement to dispense with the accompanying Medication Guide.

    Product
    Nabumetone Tablets, USP, 500 mg, 100 Tablets per carton (10 tablets x 10 blister cards), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC carton: 60687-374-01, NDC unit dose: 60687-374-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·20T012000·2020-06-30

    Bridgestone Recalls Mobile Crane Tires Due to Missing Safety Markings

    Bridgestone is recalling specific V-Steel tires for mobile cranes because they lack required DOT and safety markings, potentially leading to unsafe operating conditions.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V376000·2020-06-26

    Forest River Rockwood Trailers Recalled for Incorrect Weight Rating Labels

    Forest River is recalling 2020-2021 Rockwood trailers with incorrect Gross Axle Weight Rating information on their Federal Placards. This could allow operators to unknowingly overload the vehicle, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2361-2020·2020-06-24

    Abaxis Recalls Piccolo Xpress Chemistry Analyzers Due to Incorrect Reference Ranges

    Abaxis Inc is recalling 15 Piccolo Xpress chemistry analyzers because they display incorrect reference ranges for analytes, which may affect test result interpretation.

    Product
    Piccolo Xpress chemistry analyzer, Model No. 1100-1001, Software version 2.1.55 (NGA)/3.1.35(Jen II)
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Drugs)·D-1324-2020·2020-06-24

    Gaviscon Extra Strength Liquid Antacid Recalled for Missing Magnesium Warning

    GSK is recalling Gaviscon Extra Strength Liquid Antacid because the bottle label is missing a required magnesium safety warning.

    Product
    Gaviscon Extra Strength Liquid Antacid Extra Strength Cherry, 12 FL OZ. (355 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0574-41
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1325-2020·2020-06-24

    Gaviscon Liquid Antacid Recalled for Missing Magnesium Safety Warning

    Gaviscon Liquid Antacid Extra Strength is being recalled because the bottle label lacks a required magnesium safety warning. The recall covers single and twin-pack bottles distributed nationwide.

    Product
    GAVISCON — GAVISCON (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2402-2020·2020-06-24

    Diasol Recalls Liquid Acid Concentrate for Hemodialysis Due to Labeling Error

    Diasol, Inc. is recalling 212 cases of liquid acid concentrate for hemodialysis because of incorrect labeling of the dialysate concentration.

    Product
    DIASOL 1000225-10-DEX100 LIQUID ACID CONCENTRATE FOR BICARBONATE DIALYSIS
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1322-2020·2020-06-24

    Gaviscon Antacid Recalled for Missing Magnesium Safety Warning

    GSK is recalling Gaviscon Regular Strength Liquid Antacid bottles because the labels lack a required magnesium safety warning.

    Product
    GAVISCON — GAVISCON (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1323-2020·2020-06-24

    Gaviscon Antacid Recalled for Missing Magnesium Safety Warning

    Gaviscon Regular Strength Liquid Antacid is being recalled because the bottle label lacks the required magnesium safety warning.

    Product
    GAVISCON — GAVISCON (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowNHTSA·20V372000·2020-06-24

    Volkswagen Recalls Two 2018 Golf GTI Vehicles for VIN Label Mismatch

    Volkswagen is recalling two 2018 Golf GTI vehicles because the VIN on the Federal Certification label may not match the actual vehicle VIN, potentially preventing owners from identifying safety recalls.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2370-2020·2020-06-24

    Abbott Vascular Recalls Xience Sierra Stents Due to Incorrect Expiration Date

    Abbott Vascular is recalling 13 units of Xience Sierra coronary stents because they bear an incorrect expiration date.

    Product
    Xience Sierra TM Everolimus Eluting Coronary Stent System, RX 3.5mm x 33mmStrength: 100 ¿g/cm¿, Nominal Everolimus Content: 209 ¿g; Lot number 903224A,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0977-2020·2020-06-17

    La Sonorense Gorditas Recalled for Missing Wheat Allergen Labeling

    La Sonorense, Inc. is recalling 247 packs of Gorditas Sonora Style in Arizona due to missing wheat allergen labeling.

    Product
    La Sonorense Tortilla Factory, Gorditas Sonora Style, One Dozen, NET WT. 1 lb. 6 oz. (22 oz.)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0976-2020·2020-06-17

    La Sonorense Flour Burrito Tortillas Recalled for Wheat Allergen Mislabeling

    La Sonorense, Inc. is recalling flour burrito tortillas sold in Arizona because the packaging did not properly list wheat as an allergen.

    Product
    La Sonorense Tortilla Factory, Flour Burrito Size, One Dozen, NET WT. 1 lb. 6 oz. (22 oz.)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2287-2020·2020-06-17

    Alcon Recalls AcrySof IQ Intraocular Lenses Due to Incorrect Diopter

    Alcon Research LLC is recalling 84 units of AcrySof IQ intraocular lenses because they have an incorrect diopter. The lenses were distributed nationwide.

    Product
    Acrysof, IQ IOL w/UltraSert System, AcrySof IQ ASPHERIC IOL, 20.5 D, SP ACRYLIC FOLDABLE LENS, w/UltraSert DELIVERY SYSTEM, UV w/BLUE LIGHT FILTER. 13.0mm. LENGTH, 6.0mm ANTERIOR ASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2286-2020·2020-06-17

    Ormco Damon Q2 Orthodontic Bracket Recalled for Packaging Labeling Error

    Ormco/Sybronendo is recalling 2,189 units of Damon Q2 Orthodontic Metal Brackets because the bracket torque was mislabeled on the packaging.

    Product
    Ormco Damon Q2 Orthodontic Metal Bracket, Part No. 491-9834, L3R Hi Tq Hook, Tq +13 degrees, Rx. Manufactured by Ormco Corporation, This device is intended for use for the orthodontic movement of teeth. It is used temporarily and is removed after orthodontic treatment has bee
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V358000·2020-06-16

    Recreational vehicles with incorrect automatic parking function manual

    Forest River, Coachmen, and Dynamax recreational vehicles have an Operator's Manual that incorrectly describes the automatic parking function, potentially causing drivers to rely on it incorrectly and risking vehicle rollaway or movement.

    Product
    DYNAMAX — DYNAMAX, FOREST RIVER, COACHMEN ISATA, SUNSEEKER, BATTISTI, PRISM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2207-2020·2020-06-10

    Nobel Biocare Recalls Dental Implants Due to Incorrect Length Labeling

    Nobel Biocare is recalling 221 dental implants because the label may incorrectly state the length as 11.5mm instead of the actual 15mm, posing a risk of nerve damage.

    Product
    NobelActive Internal NP 3.5x15mm Endosseus dental implant, REF: 34128, Rx Only, Sterile R, CE, UDI: (01)07332747010619
    Category
    Medical Device
    Distribution
    28 states