The Recall Desk

Hazard

Mis Labeling recalls

9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,622
Critical
163
Severe
590
Most recent
2026-09-24

Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (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.

9326–9350 of 9622

  • LowFDA (Devices)·Z-2425-2012·2012-09-26

    Kimberly-Clark Recalls Non-Commercial Sterile Surgical Gowns

    Kimberly-Clark is recalling 32 cases of sterile surgical gowns that were not intended for commercial distribution to end users.

    Product
    ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File. The Kimberly-Clark ULTRA Fabric Reinforced Surgical Gown is a sterile, single use surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body flui
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2394-2012·2012-09-26

    Amsino Medical Recalls Mislabeled 0.9% Sodium Chloride Flush Syringes

    Amsino Medical USA is recalling one lot of 0.9% Sodium Chloride Flush syringes that may be mislabeled as 10 mL instead of 3 mL.

    Product
    0.9% Sodium Chloride Injection, USP, Pre-Filled Flush Solution, 10 mL in 12 mL Single Use Syringe, Rx only, List no. 1078-20, made in Nashville, TN, manufactured for Hospira, Inc., Lake Forest, IL 60045 USA. Flush syringe.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-2393-2012·2012-09-26

    Amsino Medical Recalls Mislabeled 0.9% Sodium Chloride Flush Syringes

    Amsino Medical USA is recalling one lot of 0.9% Sodium Chloride Flush syringes that may be mislabeled as 10 mL instead of 3 mL.

    Product
    0.9% Sodium Chloride Injection, USP, Pre-Filled Flush Solution, 3 mL in 12 mL Single Use Syringe, Rx only, List no. 1078-33, made in Nashville, TN, manufactured for Hospira, Inc., Lake Forest, IL 60045 USA. Flush syringe.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F2225-2012·2012-09-19

    Thai Farmer Brand Preserved Star Gooseberry Recalled for Undeclared Dye

    T.F. Foods Incorporated is recalling Thai Farmer Brand Preserved Star Gooseberry because it contains undeclared FD&C Yellow #6.

    Product
    Thai Farmer Brand Preserved Star Gooseberry, NET WT 7.0 OZ. Packaged 30 per case. Product labeling reads in part:"***THAI FARMER BRAND PRESERVED STAR GOOSEBERRY*** DISTRIBUTED BY: T.F. FOODS, INC. PARAMOUNT, CA 90723***NET WT. 7.0 OZ***PRODUCT OF THAILAND***".
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2340-2012·2012-09-19

    Elekta Agility Multileaf Collimator Recall for Missing Compatibility Information

    Elekta is recalling two Agility Multileaf Collimators because the original product information did not specify compatibility with the Dynamic Multileaf Collimator Apex add-on.

    Product
    Multileaf Collimator To be used for single or multiple fractions, delivered as static and/or dynamic beams of radiation, in all areas of the body where such treatment is indicated.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2337-2012·2012-09-19

    Advanced Sterilization Products Recalls STERRAD 100S and NX Cassettes

    Advanced Sterilization Products is recalling STERRAD 100S and NX cassettes because a camera used to verify printing was disabled, resulting in unverified product labels.

    Product
    STERRAD 100S Cassette, Batch # 12A077. The STERRAD 100S and STERRAD NX sterilizations systems are low-temperature general purpose sterilizers used to sterilize heat and moisture sensitive reusable medical devices. The sterilant used is hydrogen peroxide supplied in cassette fo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2296-2012·2012-09-19

    Meijer Brand Mushrooms Recalled for Sodium Labeling Error

    Meijer Distribution, Inc. is recalling Meijer Brand Mushrooms because the sodium content is above the declared value on the label.

    Product
    Meijer Brand Mushrooms, imported from The Netherlands Stems & Pieces, DR WT 4-oz and 8-oz sizes/Net Wt. 6.5-oz and 13.25-oz, UPC 7-1373337545-0 and UPC 7-1373337544-3
    Category
    Food
    Distribution
    5 states
  • LowFDA (Devices)·Z-2338-2012·2012-09-19

    Advanced Sterilization Products Recalls STERRAD NX Cassettes Due to Printing Verification Failure

    Advanced Sterilization Products is recalling STERRAD NX cassettes because the camera used to verify printing was disabled, resulting in unverified product labels.

    Product
    STERRAD NX Cassette, Batch # 12A078. The STERRAD 100S and STERRAD NX sterilizations systems are low-temperature general purpose sterilizers used to sterilize heat and moisture sensitive reusable medical devices. The sterilant used is hydrogen peroxide supplied in cassette form
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2336-2012·2012-09-19

    Helix Medical Recalls Blom-Singer Occluder for Invalid Expiration Date

    Helix Medical LLC is recalling the Blom-Singer indwelling TEP Occluder due to an invalid expiration date. The recall covers devices distributed in the US and UK.

    Product
    BLOM-SINGER indwelling TEP Occluder, catalog IN2004-TO The Blom-Singer Indwelling (TEP(tracheoesophageal Puncture) Occluder is a non-valved silicone prosthesis designed for placement in and maintenance of the TE (tracheoesophageal) puncture following total laryngectomy. The Bl
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2118-2012·2012-09-12

    Bissinger's Campfire S'Mores Salt Caramels Recalled for Gluten Mislabeling

    Karl Bissinger Inc is recalling Bissinger's Campfire S'Mores Salt Caramels because the product is labeled as gluten-free but contains wheat.

    Product
    Bissinger's Campfire S'Mores Salt Caramels, packaged in 1.8-oz. boxes, 5 pieces per box, 12 boxes per display case, UPC 846107012788. The firm name on the label is Bissinger's Handcrafted Chocolatier, St. Louis, MO.
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-2129-2012·2012-09-12

    Clif Bar Recalls Blueberry Crisp Bars Due to Mislabeling

    Clif Bar and Company is recalling Blueberry Crisp CLIF Bars because some were mistakenly packaged in Chocolate Chip wrappers.

    Product
    Blueberry Crisp CLIF Bars, 12 pack boxes, UPC: 7-22252-30260-1
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2326-2012·2012-09-12

    Breg Polar Dressing Recalled for Thickness and Durability Defects

    Breg Inc. is recalling Polar Dressing units that are thinner than specified, making them less durable and prone to tearing.

    Product
    Polar Dressing, Knee/MU/Shldr Intelli-Flo-Breg, PN 10630 Used with cold therapy pads to provide insulation barrier between the pad and patient's skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2130-2012·2012-09-12

    Clif Bar Recalls Chocolate Chip Bars Due to Incorrect Packaging

    Clif Bar and Company is recalling 4,608 Chocolate Chip CLIF Bars because some Blueberry Crisp bars were mistakenly placed in Chocolate Chip wrappers.

    Product
    Chocolate Chip CLIF Bars, 2.4-oz (68g), individually wrapped, UPC: 7-22252-10090
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2323-2012·2012-09-12

    Trek Diagnostic Systems Recalls VersaTREK Windows Software Version 5.4.3

    Trek Diagnostic Systems is recalling VersaTREK Windows Software Version 5.4.3 because positive test results may incorrectly revert to negative in the database.

    Product
    VersaTREK Windows Software, Version 5.4.3 is a component of the VersaTrek System. The Software CD will be individually packaged using a standard CD plastic case and placed into a standard CD mailer The VersaTREK System is for cultivating and recovering microorganisms, especial
    Category
    Medical Device
    Distribution
    38 states
  • ModerateFDA (Devices)·Z-2308-2012·2012-09-12

    Princeton Biomeditech Recalls Status Flu A + B Test Kits

    Princeton Biomeditech is recalling 90 kits of the Status Flu A + B Test due to reports of dual positive results.

    Product
    Status Flu A + B Test Manufactured by Princeton Bio Meditech Corporation Monmouth Junction, NJ 08852 USA. The BioSign Flu A + B test is an in vitro rapid qualitative test that detects influenza type A and type B nucleoprotein antigens directly from nasal swab, nasopharynge
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2119-2012·2012-09-12

    CLIF Bar Coconut Chocolate Chip Bars Recalled for Undeclared Coconut

    Clif Bar and Company is recalling Coconut Chocolate Chip bars due to undeclared coconut in the ingredient statement.

    Product
    CLIF Bar Brand Coconut Chocolate Chip CLIF Bars, 6-pack boxes, UPC: 7-22252-66030-5 Product is manufactured by Harlan Bakeries in Indianapolis, IN.
    Category
    Food
    Distribution
    0 states
  • LowFDA (Devices)·Z-2314-2012·2012-09-12

    Quality Electrodynamics Recalls 17 Non-Functional MRI Knee Coils

    Quality Electrodynamics LLC is recalling 17 TxRx Knee 15 Coil 3T units because the coil identification code is incorrect, rendering the devices non-functional.

    Product
    TxRx Knee 15 Coil 3T. For use in conjunction with magnetic resonance scanners to produce diagnostic images of the knee that can be interpreted by a trained physician.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2098-2012·2012-09-05

    Honey Heaven Wholesale Recalls Organic Pinenuts Due to Peanut Contamination

    Honey Heaven Wholesale, Inc. is recalling Organic Pinenuts due to potential contamination with peanuts or traces of peanuts. The product was distributed to retail stores in California, Oregon, and Washington.

    Product
    Organic Pinenuts. 5lb bag: Organic Pine nuts packed into plastic bag with a twist tie with a White stick on label with hand written product description. 27.5lb bag: Organic Pine nuts inside of a plastic bag with a white stick on label with typed product description.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2038-2012·2012-09-05

    Cass-Clay Creamery Recalls Ice Cream for Undeclared Soy and Wheat

    Cass-Clay Creamery is voluntarily recalling specific ice cream products because they may contain undeclared soy lecithin and wheat.

    Product
    CASS-CLAY: LIGHT DUSTY ROAD, ONE GALLON (3.78 L), 0 70422 23480 2. LIGHT ICE CREAM, DUSTY ROAD, HALF GALLON (1.89L), 0 70422 24080 3
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2056-2012·2012-09-05

    Cass-Clay Creamery Recalls Ice Cream for Undeclared Peanuts

    Cass-Clay Creamery is voluntarily recalling specific ice cream products because they may contain undeclared peanuts, posing a risk to consumers with peanut allergies.

    Product
    Hornbachers, Peanut Butter Fudge, Half Gallon, (1.89L), 0 41130-21659 6.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2057-2012·2012-09-05

    Cass-Clay Creamery Recalls Swiss Chip Ice Cream for Undeclared Soy

    Cass-Clay Creamery is voluntarily recalling Swiss Chip ice cream because it may contain undeclared soy lecithin. The recall affects 81 containers distributed in five states.

    Product
    Cass-Clay , Swiss Chip, 3 Gallon(11.34 L).
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2046-2012·2012-09-05

    Cass-Clay Creamery Recalls Ice Cream for Undeclared Soy

    Cass-Clay Creamery is voluntarily recalling specific ice cream products because they may contain undeclared soy lecithin.

    Product
    Cass-Clay, UND CHAMPION CHIP, half gallon (1.89 L) 0 70422 04062 5 Cass-Clay, UND CHAMPION CHIP 3 Gallon (11.34 L)
    Category
    Food
    Distribution
    5 states