The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 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 589 (6%) are Severe.

Which agencies issued them

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.

6351–6375 of 9611

  • ModerateFDA (Devices)·Z-1845-2015·2015-07-01

    Volcano Prestige Plus J-Tip Wire Recalled for Incorrect Shelf Life Labeling

    Volcano Corporation is recalling 162 Prestige Plus 185cm J-Tip pressure wires because they were labeled with incorrect shelf life dates during a relabeling procedure.

    Product
    Prestige Plus 185cm J-Tip: Part number: 9185J; Product Usage: The Prestige Plus Wire is indicated for use to measure pressure in blood vessels including both coronary and peripheral vessels, during diagnostic angiography and/or any interventional procedures. Blood pressure m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2733-2015·2015-07-01

    Golden Chocolate Papaya Recalled for Undeclared Food Colorings

    Golden Chocolate International is recalling 513 lbs of ROGALIK PAPAYA due to undeclared FD&C food colorings. The product was distributed in New York and Pennsylvania.

    Product
    Golden Chocolate ROGALIK PAPAYA, Net Wt. 1Lb. (454 g). Manufactured for and Distributed by: Golden Chocolate, Brooklyn, NY 11231.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1824-2015·2015-07-01

    CooperSurgical Recalls Vaginal Speculums Due to Incorrect Packaging

    CooperSurgical is recalling 9,400 McKesson Medi-Pak Vaginal Speculums because small-sized speculums were incorrectly packaged in bags labeled for medium-sized speculums.

    Product
    McKesson Medi-Pak Vaginal Speculum, 10/bag Reorder No. 11-8309 Used to expose interior of the vagina to facilitate visualization during gynecological and obstetrical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1826-2015·2015-07-01

    Merit Medical Prelude Pro Sheath Introducer Recalled for Incorrect Dilator Packaging

    Merit Medical Systems is recalling Prelude Pro Sheath Introducers packaged with a 0.035-inch dilator instead of the labeled 0.038-inch size.

    Product
    Merit Medical Prelude Pro Sheath Introducter, 6F (2.0mm) 11cm, REF PRO-6F-11-038, Sterile EO The Merit Prelude Sheath Introducer is intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries while maintaining hemostasis
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1844-2015·2015-07-01

    Volcano PV .035 Catheter Recalled for Incorrect Shelf Life Labeling

    Volcano Corporation is recalling 162 PV .035 Catheters because they were labeled with incorrect shelf life dates during a relabeling procedure.

    Product
    Volcano PV .035 Catheter: Part number: 88901; Product Usage: The Volcano PV .035 is indicated for use in the evaluation of vascular morphology in blood vessels of the peripheral vasculature by providing a cross-sectional image of such vessels. The device is an adjunct to con
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1830-2015·2015-07-01

    Cook Inc. Recalls LapSac Surgical Tissue Pouches Due to Labeling Error

    Cook Inc. is recalling 123,184 LapSac Surgical Tissue Pouches because the labeling includes information not stated in the intended use.

    Product
    LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue during, or prior to, surgical removal and/or morcellation. The device is a reinforced pouch with an inner liner and drawstring closure. The device may be used t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1840-2015·2015-07-01

    Bio-Rad Anti-HBs Cutoff Calibrator Recalled for Incorrect Expiration Date

    Bio-Rad Laboratories is recalling 20 vials of Anti-HBs Cutoff Calibrator because the expiration date printed on the label is incorrect.

    Product
    The spare component Anti-HBs Cutoff Calibrator, 10 mLU/mL, Catalog number 26154. The spare component is sold separately from the MONOLISA Anti-HBs EIA Kit contains an expiration date of 2016-04-30 in error.
    Category
    Medical Device
    Distribution
    5 states
  • LowFDA (Drugs)·D-1148-2015·2015-07-01

    Actavis Recalls Lutera Birth Control Due to Outdated Package Inserts

    Actavis Inc is recalling Lutera birth control tablets because the packs were distributed with out-dated package inserts.

    Product
    Lutera (0.1 mg levonorgestrel and 0.02 mg ethinyl estradiol tablets USP), 28 day Regimen, 6 Tablet Dispensers per box, 28 Tablets Each, Rx Only, Manufactured for: Watson Pharm, Inc., a subsidiary of Watson Pharmaceutical, Inc., Corona, CA 92880, Manufactured by: Patheon, Inc., Mi
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1839-2015·2015-07-01

    Ethicon Recalls Surgical Sutures Due to Incomplete Labeling

    Ethicon is recalling specific lots of Fast Absorbing Plain Gut sutures because the box and foil labels are incomplete.

    Product
    Ethicon Fast Absorbing Plain Gut - MultiPass Needles, Sterile, Absorbable Surgical Suture, 5-0 (1.5 metric), 18" (45 cm), Conventional Cutting, Lot #JD6163, Exp: July 2019. Fast absorbing surgical gut suture is a strand of collagenous material prepared from the submucosal layers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2441-2015·2015-06-24

    Whole Foods Market Muffin Bran Recalled for Undeclared Milk and Eggs

    Whole Foods Market is recalling Muffin Bran 6Pk packages due to undeclared milk and eggs. Consumers should check their pantries for affected products.

    Product
    BRAN Whole Foods Market Muffin Bran 6Pk packaged in clear plastic "clam shell" containers, NET WT. 12 oz., PLU 24857800499 Dist. by Whole Foods Market Austin, TX 78703
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1807-2015·2015-06-24

    Philips Q-Station Ultrasound Software Recalled for Data Integrity Issues

    Philips is recalling Q-Station ultrasound software because patient measurements may be incorrectly appended to other patients' studies.

    Product
    Philips Ultrasound, Model Q-Station, with software version 3 or higher, Catalog number: 795088; Part Number: 989605382391 Q-Station is application software intended to manage, view, analyze, and report qualitative and quantitative image data from ultrasound exams. It is desig
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1796-2015·2015-06-24

    Mortara ELI 380 Electrocardiograph Recalled for Patient Data Mismatch Risk

    Mortara Instrument is recalling 176 ELI 380 electrocardiographs because ECG waveforms may be incorrectly associated with the wrong patient's demographics when transmitted to records systems.

    Product
    ELI 380 Electrocardiograph. The ELI 380 is intended to be a high-performance, multichannel resting electrocardiograph. As a resting electrocardiograph, the ELI 380 simultaneously acquires data from each lead. Once the data is acquired, it can be analyzed, reviewed, stored, prin
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-2439-2015·2015-06-24

    Byrds Famous Cookies Recalled for Undeclared Anchovies

    Byrd Cookie Company is recalling Vidalia Onion Biscuits because they contain undeclared anchovies, a common allergen.

    Product
    Byrds Famous Cookies, Vidalia Onion Biscuits, Net Wt. 3 oz. and 6 oz. tins, UPC: 0-74882904599-3 (6 oz) and 0-74882904605-1 (3 oz), Byrd Cookie Company, P.O. Box 1308, Savannah, GA 31416.
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1800-2015·2015-06-24

    Synthes Recalls 3.7mm Cannulated Screws Due to Incorrect Labeling

    Synthes, Inc. is recalling 54 units of 3.7mm Cannulated Locking and Conical Screws because certain lots were found to have been labeled incorrectly.

    Product
    3.7mm Cannulated Locking Screws and 3.7mm Cannulated Conical Screws; . the Cannulated Screws are indicated for fixation of fractures, osteotomies, and non-unions of the clavicle, scapula, olecranon, humerus, radius, ulna, pelvis, tibia, and fibula, particularly in osteopenic bon
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1814-2015·2015-06-24

    CooperSurgical Recalls MILEX OMNIFLEX Diaphragms Due to Packaging Error

    CooperSurgical is recalling 200 units of MILEX OMNIFLEX Diaphragms because size 80 boxes were incorrectly packaged with size 85 diaphragms.

    Product
    MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-1808-2015·2015-06-24

    AMUSA Sterile Field Flush Syringe Recalled for Incorrect Expiration Date Labeling

    MRP, LLC dba AMUSA is recalling 1,080 units of T/S2 0.9% Sodium Chloride Injection flush syringes due to incorrect expiration date labeling.

    Product
    T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush syringe.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1798-2015·2015-06-24

    Biomet Vanguard M Unicondylar Tibial Trial Recalled for Incorrect Etching

    Biomet, Inc. is recalling 27 Vanguard M Unicondylar Tibial Trials because the left and right orientation markings are incorrectly etched on the handle.

    Product
    Vanguard M Unicondylar Tibial Trial For use during knee joint replacement.
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·15V400000·2015-06-23

    Starcraft RV Recalls 2014-2016 Trailers for Incorrect Tire Certification Labels

    Starcraft RV is recalling 50 model year 2014-2016 AR-ONE and Comet trailers because certification labels list the wrong tire size, which could lead to improper tire installation and increased crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT, STARCRAFT COMET, AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2436-2015·2015-06-17

    AYAA Corn Cake Recalled for Undeclared Milk Allergen

    AYAA Popcorn Manufacturing Corp. is recalling Corn Cake 10 oz and 14 oz packages because FDA inspection found undeclared milk on the labels.

    Product
    Corn Cake 10 oz and 14 oz
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-2433-2015·2015-06-17

    Sugar Free Vanilla Cake Recalled for Undeclared Milk Allergen

    AYAA Popcorn Manufacturing Corp. is recalling Sugar Free Vanilla Cake 2 oz. because FDA inspection found undeclared milk on the labels.

    Product
    Sugar Free Vanilla Cake 2 oz.
    Category
    Food
    Distribution
    0 states