The Recall Desk

Hazard

Mislabeling recalls

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

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mislabeling 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.

226–250 of 256

  • ModerateFDA (Devices)·Z-0636-2022·2022-02-16

    Microbiologics Recalls KWIK-STIK Microorganism Reference Material Due to Organism Mislabeling

    Microbiologics Inc is recalling KWIK-STIK microorganism reference kits labeled as Actinomyces odontolyticus but containing Eggerthella lenta. The mislabeling could cause incorrect organism identification in laboratory testing.

    Product
    KWIK-STIK(TM) labeled as containing Actinomyces odontolyticus. Each KWIK-STIK" unit contains a lyophilized pellet of a single microorganism strain, a reservoir of hydrating fluid and an inoculating swab. Each device is sealed within a laminated pouch that contains a desiccan
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0637-2022·2022-02-16

    LYSO Disk microorganism culture device mislabeled with incorrect strain

    Microbiologics' LYSO Disk culture disks labeled as containing Actinomyces odontolyticus have been found to actually contain Eggerthella lenta. The mislabeling affects products distributed to Canada and Germany.

    Product
    LYSO Disk(TM) labeled as containing Actinomyces odontolyticus. Each LYSO Disk" unit contains six lyophilized pellets of a single microorganism strain, in a glass vial. Each vial is sealed and contains a desiccant to prevent adverse moisture accumulation. A LYFO Disk" catalog
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Drugs)·D-0522-2022·2022-02-09

    Prescription Drug Recall: Mimvey Mislabeling by Teva Pharmaceuticals

    Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) tablets nationwide due to mislabeling. The recall affects 6,430 cartons distributed throughout the USA.

    Product
    MIMVEY — MIMVEY (ESTRADIOL AND NORETHINDRONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0521-2022·2022-02-02

    Inglehoffer Seafood Tartar Sauce Recalled for Undeclared Soy

    Beaverton Foods Inc is recalling Inglehoffer Seafood Tartar Sauce with Lemon & Capers because the ingredient label declares soybean oil but does not adequately disclose soy as an allergen, posing a risk to consumers with soy allergies.

    Product
    Inglehoffer Seafood Tartar Sauce With Lemon & Capers, 8.25oz (234g) jar, UPC 0 71828 01114 1. The label is read in parts: "***Inglehoffer*** Seafood TARTAR SAUCE WITH LEMON & CAPERS*** INGREDIENTS: SOYBEAN OIL, WATER, CUCUMBERS, EGGS, WHITE DISTILLED VINEGAR, SALT, MUSTARD SEE
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0383-2022·2022-01-19

    Renaissance Food Group Chicken Salad Croissants Contain Undeclared Tuna Salad

    Renaissance Food Group is recalling Chicken Salad Croissants because some packages contain Tuna Salad, which is not declared on the label. Fish is a major allergen and poses a serious risk to consumers with fish allergies.

    Product
    CHICKEN SALAD Croissant NET WT. 7.8OZ (221g) Perishable, Keep Refrigerated Ingredients: Chicken Salad***Savory Mayonnaise Base***Croissant***Lettuce. CONTIANS EGG, MILK, WHEAT, SOY, MAY CONTAIN TREE NUTS. Dist. By: Renaissance Food Group, LLC 4322 Moreland Ave. Conley, GA 30288 U
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0366-2022·2022-01-19

    Howling Cow Butter Almond Ice Cream recalled for undeclared allergens

    Howling Cow Butter Almond ice cream sold in North Carolina and South Carolina contains Cookie Dough Ice Cream with undeclared soy and wheat allergens. Consumers with allergies should not consume the product.

    Product
    butter almond HOWLING COW THE ICE CREAM OF NC STATE UNIVERSITY One Pint (473 ml) Ingredients: Milk, Cream, Sugar, Almonds***Stabilizer***Carmel Color and Natural Flavor. Contains milk, almonds Proudly distributed by Hunter Farms High Point, NC 27262 UPC 0 74336 65079 6
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0391-2022·2022-01-19

    Classic Lasagna Pasta Sheets Recalled for Undeclared Wheat Allergen

    Local Fixe LLC is recalling Classic Lasagna Pasta sheets because the label declares flour as an ingredient but fails to declare wheat, which is present in the product. Consumers with wheat allergies may face serious health risks.

    Product
    Classic Lasagna Pasta sheets sold frozen and wrapped in brown freezer paper. The weight per package is 1 lb/453.6 grams. The label is read in parts: "***Classic Lasagna sheets *** Ingredients: Flour, Semolina, Egg, water ***www.localfixe.com***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0387-2022·2021-12-22

    Cook Flexor Check-Flo Introducer recalled for size mislabeling

    Cook Inc. is recalling the Flexor Check-Flo Introducer due to mislabeled packaging where 6FR devices may be labeled as 7FR or vice versa. This size mislabeling could result in selection of the wrong device size.

    Product
    Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-6.0-18/38-45-RB-ANL0-HC Order Number/GPN: G44154 Intended to introduce therapeutic or diagnostic devices into the vasculature, excluding coronary and neuro vasculature.
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-0388-2022·2021-12-22

    Flexor Check-Flo Introducer Recalled for Mislabeled Caliber Size

    Cook Inc. is recalling Flexor Check-Flo Introducer devices due to mislabeling where packages marked as 6FR may contain 7FR devices, or vice versa. This sizing mismatch could result in improper device selection during clinical vascular procedures.

    Product
    Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-7.0-18/38-45-RB-ANL0-HC Order Number/GPN: G44155 Intended to introduce therapeutic or diagnostic devices into the vasculature, excluding coronary and neuro vasculature.
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-0275-2022·2021-12-01

    da Vinci Surgical Drapes Recalled for Incorrect Expiration Date on Packaging

    Intuitive Surgical recalls 1,740 da Vinci Instrument Arm Drapes due to incorrect expiration dates on package labeling. The error may prevent accurate verification of sterility assurance dates.

    Product
    The da Vinci Xi and X surgical systems (IS4000 and IS4200) each consist of three main components: the Surgeon Console (SC), the Vision Cart (VC), and the Patient Cart (PC). The Patient Cart is the operative component of the system and its primary function is to support the instru
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0120-2022·2021-11-10

    Mountain View Bakery Chocolate Cake Roll Recall for Undeclared Milk

    Mountain View Bakery is recalling Chocolate Cake Rolls (4oz and 8oz) distributed to Pilot gas stations in Tennessee because the product contains undeclared milk, a common allergen.

    Product
    Mountain View Bakery Chocolate Cake Roll 4oz or 8oz packaged in plastic clamshell sold individually
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0108-2022·2021-11-10

    Picket Fence Creamery Cheese Curds Recalled for Undeclared Soy

    Picket Fence Creamery is recalling Bacon-Ranch White Cheddar cheese curds due to undeclared soy lecithin. The product may pose a risk to consumers with soy allergies.

    Product
    Picket Fence Creamery, Woodward, IA, Bacon-Ranch White Cheddar cheese curds, Net Wt. 12 oz, UPC 094922414984
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0170-2022·2021-11-03

    GORE CARDIOFORM Septal Occluder Recalled for Incorrect Expiration Date Labeling

    W L Gore & Associates is recalling 187 units of GORE CARDIOFORM Septal Occluders because they are labeled with a 3-year expiration date instead of the correct 2-year expiration date. Using the device beyond its actual shelf life could compromise its safety and effectiveness.

    Product
    REF/Catalogue Number GSXE0025B, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132620111 *Not distributed within the US
    Category
    Medical Device
    Distribution
    47 states
  • ModerateFDA (Devices)·Z-0167-2022·2021-11-03

    GORE CARDIOFORM SEPTAL OCCLUDER Recalled for Incorrect Expiration Date Labeling

    GORE CARDIOFORM SEPTAL OCCLUDER devices are recalled for labeling errors: 95 units marked with 3-year expiration instead of correct 2-year date. Affected units distributed across US and international locations.

    Product
    REF/Catalogue Number GSXE0020, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617630 *Not distributed within the US
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Devices)·Z-0159-2022·2021-10-27

    Orthopedic Bone Screws Recalled Due to Potential Length Mislabeling

    Limacorporate S.p.A is recalling 151 units of bone screws because the labeled length may not match the actual screw length included in the package.

    Product
    REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE R, 2100099, UDI: (01)08033390018852
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2617-2021·2021-10-06

    Xcela PICC catheter mislabeled with incorrect size designation

    Angiodynamics is recalling Xcela PICC catheters where units labeled as 5F are actually 4F. The labeling discrepancy between labeled and actual product size could affect clinical device selection.

    Product
    Xcela PICC with PASV Valve Technology/Kit 5 F-55cm; (Maximum Flow Rate 3.5 mL/Sec)-indicated for short or long-term peripheral access to the central venous system for intravenous therapy, including but not limited to, the administration of fluids, medications, and nutrients; the
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Drugs)·D-0771-2021·2021-09-01

    Bleomycin for Injection Recalled Due to Mislabeling

    Hikma Pharmaceuticals USA Inc. is recalling Bleomycin for Injection, USP due to mislabeling. The recall affects 1,152 vials distributed nationwide.

    Product
    BLEOMYCIN — BLEOMYCIN (BLEOMYCIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0752-2021·2021-08-25

    Triamcinolone Acetonide Ointment Mispack Recall by Teligent Pharma

    Teligent Pharma is recalling Triamcinolone Acetonide Ointment USP 0.1% due to a labeling mispack affecting Lot #16630 with expiration 03/2023. The recall was issued due to incorrect labeling on the product.

    Product
    Triamcinolone Acetonide Ointment USP, 0.1% 80 g cartons, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-014-80 ; packaged in tubes.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0871-2021·2021-08-18

    Dark Chocolate Malt Balls recalled for undeclared peanuts

    DSD Merchandisers is recalling Dark Chocolate Malt Balls because some containers were filled with Dark Chocolate Peanut Butter malt balls instead, creating a risk for consumers with peanut allergies who may not be aware of the peanut content.

    Product
    Dark Chocolate Malt Balls in plastic container; 9 oz./ 255g UPC: 6 5143370179 0 Packed on the same equipment as products that contain milk, eggs, tree nuts, peanuts, wheat and soy. Distributed by DSD Merchandisers, Inc., Livermore, CA 64551
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2229-2021·2021-08-18

    Shent USA Grasper/Retriever Endoscopic Instruments Recalled for Mislabeling

    Shent USA is recalling Grasper/Retriever endoscopic instruments (lot 020377208) due to mislabeling. Products bearing one catalog number may contain different devices with different jaw specifications, potentially resulting in wrong instrument selection.

    Product
    Grasper/Retriever, Alligator Jaw 2.4 mm x 5 mm x 230 cm Catalog Number: 7208 Intended use: single use accessory devices used through the working channel of a GI endoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2230-2021·2021-08-18

    Endoscope Grasper/Retriever Devices Mislabeled with Incorrect Catalog Numbers

    Shent USA recalls grasper/retriever endoscopy devices that are mislabeled with incorrect catalog numbers. Units labeled as catalog #7208 may actually be #7226 and vice versa, potentially causing use of the wrong jaw size.

    Product
    Grasper/Retriever, Alligator Jaw, Rat Tooth 2.4 mm x 8 mm x 230 cm Catalog Number: 7226 Intended use: single use accessory devices used through the working channel of a GI endoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0794-2021·2021-07-28

    MCT Powder 70% from Coconut Recalled for Milk Allergen

    Nutralliance Inc is recalling Medium Chain Triglyceride (MCT) Powder 70% from Coconut distributed in bulk to supplement manufacturers because an ingredient tested positive for milk allergen.

    Product
    Medium Chain Triglyceride (MCT) Powder 70% from Coconut / CocoTrim packaged in 20 kilogram brown bags with plastic inner lining for bulk sale to supplement manufacturers. Exclusively Distributed by Nutralliance / Manufactured by Bio-gen Extracts Pvt. Ltd. Store tightly sealed con
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2051-2021·2021-07-21

    Medical device recall: EASYGRIP FLO-41 barcode expiration date discrepancy

    Baxter Healthcare Corporation is recalling 4,752 units of EASYGRIP FLO-41 hemostatic delivery devices due to a discrepancy between the expiration date encoded in the 2D barcode and the human-readable date on the product.

    Product
    EASYGRIP FLO-41 US. For delivering hemostatic agents to bleeding sites through a trocar.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2024-2021·2021-07-14

    Vivorte Bone Void Filler Recalled for Incorrect Expiration Date

    Vivorte, Inc. is recalling Trabexus EB bone filler due to an incorrect expiration date on product labels. The label shows expiration of 02-15-2019, but the actual expiration is 12-18-2018.

    Product
    Vivorte Trabexus EB 10 cc Bone Void Filler -Fill bone and/or defect in skeletal system Model Number: 130703-10
    Category
    Medical Device
    Distribution
    1 state