The Recall Desk

Hazard

Mis Labeling recalls

9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,606
Critical
160
Severe
588
Most recent
2026-09-09

Of the 9,606 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.

1301–1325 of 9606

  • HighFDA (Food)·F-0100-2022·2021-11-10

    Picket Fence Creamery Mocha Ice Cream Recalled for Undeclared Soy

    Picket Fence Creamery is recalling Mocha! ice cream in multiple sizes due to undeclared soy lecithin. Consumers with soy allergies who purchased this product should not consume it.

    Product
    Picket Fence Creamery, Woodward, IA, Mocha! ice cream, in Quarts, Pints, and 1/2 Pints
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0164-2022·2021-11-03

    Gore CARDIOFORM Septal Occluder recalled for incorrect expiration date

    W.L. Gore & Associates is recalling 2,238 GORE CARDIOFORM SEPTAL OCCLUDER 30 mm devices labeled with a 3-year expiration date instead of the actual 2-year expiration date.

    Product
    REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631032
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Devices)·Z-0165-2022·2021-11-03

    GORE Cardioform Septal Occluder recalled for incorrect expiration date labeling

    W.L. Gore is recalling 138 units of GORE Cardioform Septal Occluder devices labeled with a 3-year expiration date instead of the actual 2-year shelf life.

    Product
    REF/Catalogue Number GSX0020A, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631018
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Devices)·Z-0171-2022·2021-11-03

    Septal Occluder Devices Recalled for Incorrect Expiration Date Label

    W L Gore & Associates is recalling 222 GORE Cardioform Septal Occluder devices labeled with a 3-year expiration date instead of the correct 2-year expiration.

    Product
    REF/Catalogue Number GSXE0030B, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132620128 *Not distributed within the US
    Category
    Medical Device
    Distribution
    47 states
  • ModerateFDA (Devices)·Z-0168-2022·2021-11-03

    GORE CARDIOFORM Septal Occluder Labeled with Incorrect Expiration Date

    W L Gore & Associates is recalling GORE CARDIOFORM Septal Occluder devices labeled with a 3-year expiration date instead of the correct 2-year date. Mislabeling could result in use of devices beyond their intended safe lifespan.

    Product
    REF/Catalogue Number GSXE0025, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617647 *Not distributed within the US
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Food)·F-0044-2022·2021-10-27

    Chocolate & the Chip Gluten Free Cookies Recalled for Undeclared Allergens

    Chocolate & the Chip is recalling its Gluten Free Original Chocolate Chip Cookies due to undeclared milk and soy allergens found during a California Department of Public Health inspection. Consumers with allergies to milk or soy should not consume the product.

    Product
    Chocolate & the Chip Gluten free original chocolate chip: Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Ingredients: Gluten free flour (sweet white rice flour, whole grain brown
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0150-2022·2021-10-27

    Anti-Xa Assay On-Board Stability Reduced from 7 to 5 Days

    The HemosIL Liquid Anti-Xa diagnostic assay has reduced on-board stability from 7 days to 5 days. Laboratories should follow updated stability guidelines for all currently released and future lots.

    Product
    HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic use by laboratory professionals in clinical laboratories. The assay provides quantitative results on 3.2% citrated human plasma Part Number: 0020302602
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0147-2022·2021-10-27

    Central Line Dressing Kit Component Has Shorter Expiration Than Kit Label

    Medical Action Industries recalls Central Line Dressing Change kits because the ChloraPrep 3ml component expires sooner than the kit label indicates. Users should discontinue use and contact their supplier.

    Product
    Kit: Central Line Dres Change 20/Cs
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0160-2022·2021-10-27

    Bone Screw Labeling Error: Actual Length May Not Match Package Label

    Limacorporate is recalling bone screws (REF 8420.15.010) because the actual length of the screws may not correspond to the length stated on the package label, potentially affecting proper surgical placement and implant stability.

    Product
    REF 8420.15.010, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=20mm, STERILE R, 2100099, UDI: (01)08033390018845
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0037-2022·2021-10-27

    Chocolate and the Chip Peanutbutter Spice Cookies Recalled for Undeclared Allergens

    Chocolate and the Chip is recalling Peanutbutter Spice Cookies due to undeclared allergens including wheat, milk, and soy found during a California Department of Public Health inspection. Consumers with allergies to these substances should not consume the product.

    Product
    Chocolate & the Chip Peanutbutter Spice Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Ingredients: All purpose flour (bleached wheat flour, malted barley flour, niacin, reduced ir
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0036-2022·2021-10-27

    Chocolate & the Chip Octoberfest Cookies Recalled for Undeclared Allergens

    Chocolate & the Chip Octoberfest Cookies are being recalled due to undeclared wheat, milk, and soy allergens found on product labels during a California Department of Public Health inspection.

    Product
    Chocolate & the Chip Octoberfest Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Not provided. Labels found during the inspection had undeclared wheat, milk, soy. Firm had listed
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0046-2022·2021-10-27

    Chocolate & the Chip Gluten-Free Cookie Cake Recalled for Undeclared Tree Nuts

    Chocolate & the Chip is recalling its gluten-free cookie cake due to undeclared tree nuts (hazelnuts and almonds) found on the packaging labels. The product was distributed nationwide and poses a risk to consumers with tree nut allergies.

    Product
    Chocolate & the Chip Gluten free cookie cake: Cookie cakes: 1LB 1.4oz / 494 grams Packaged in a brown bakery box with window and labeled.1 unit per package. Corrected Ingredients: Not provided Labels found during the inspection had undeclared tree nuts (hazelnuts and alm
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0153-2022·2021-10-27

    Jamshidi Bone Marrow Biopsy Tray Recalled for Misbranding

    Bard Peripheral Vascular Inc is recalling an Economy Jamshidi Bone Marrow Biopsy and Aspiration Tray due to misbranding. A total of 360 devices were distributed to healthcare facilities across multiple U.S. states.

    Product
    Catalog # BEK4511, Qty: 10, Ecomomy Jamshidi Bone Marrow Biopsy and Aspiration Tray, 11 G X 4"Biopsy/Aspiration needle, 15 G Aspiration Needle (Adjustable Length 15/16" -1-7/8") (24mm-48mm) sterile, For Single Use Only, RX only. Exp. Date Lidocaine Vendor lot. CareFusion. O
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Food)·F-0048-2022·2021-10-27

    Chocolate & the Chip Rice Crispy Treats Recalled for Undeclared Allergens

    Chocolate & the Chip is recalling The OG Rice Crispy treats due to undeclared milk and soy allergens on product labels. The recall affects 3,000 units distributed nationwide.

    Product
    Chocolate & the Chip The OG Rice Crispy: Rice crispy treats: 6 oz / 171 grams Packaged in a food grade clear poly tubing, heat sealed with label Corrected Ingredients: Not provided Labels found during the inspection had undeclared milk, soy. Firm had listed ingredients o
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0154-2022·2021-10-27

    Jamshidi Bone Marrow Biopsy Tray Recalled Due to Misbranding

    Bard Peripheral Vascular Inc. is recalling 360 Jamshidi Bone Marrow Biopsy Trays (Catalog # BEK3411, Lot # 0001378561) due to misbranded labeling. The FDA classified this as a Class II recall affecting healthcare facilities in 16 U.S. states and Puerto Rico.

    Product
    Catalog # BEK3411, Ecomomy Jamshidi Bone Marrow Biopsy Tray, 11 G X 4"Biopsy/Aspiration needle, sterile, Qty: 10, Single Use Only, RX only. Exp. Date Lidocaine Vendor lot. CareFusion Intended use to aspirate marrow from either the sternum or the iliac crest. Intraosseous Inf
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-0143-2022·2021-10-27

    Smith & Nephew cannulated screw label incorrectly indicates threading type

    Smith & Nephew is recalling 6.5mm x 165mm cannulated screws because the product label incorrectly states the screws are fully threaded when they are actually partially threaded.

    Product
    6.5MMX165MM CANNULATED SCREW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·21V836000·2021-10-25

    Yamaha Recalls 2021 Tracer 9 GT for Incorrect VIN Label

    Yamaha is recalling 2021 Tracer 9 GT motorcycles because the VIN on the certification label may not match the vehicle's stamped VIN, potentially preventing owners from receiving safety recall remedies.

    Product
    YAMAHA — YAMAHA TRACER 9 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0015-2022·2021-10-20

    Frozen vegan crabcakes recalled for undeclared egg allergen

    Cuisine Innovations Unlimited, LLC is recalling Vemondo Vegan Crabless Mini Crabcakes sold at Lidl due to undeclared egg. The product may pose a risk to consumers with egg allergies.

    Product
    Vemondo Vegan Crabless Mini Crabcakes by Lidl 8.5 OUNCES (240g) coated paper box ten (10) packages per case. Frozen.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0077-2022·2021-10-20

    Gore VIABAHN VBX endoprosthesis recalled for incorrect device dimension labeling

    W L Gore & Associates is recalling GORE VIABAHN VBX balloon expandable endoprosthesis units due to labeling showing incorrect device dimensions. Two units with specification mismatches were distributed to Italy and Lebanon.

    Product
    Heparin, GORE VIABAHN VBX, BALLOON EXPANDABLE ENDOPROTHESIS, REF BXAL085902E, 8 MM X 59 MM 8 Fr, LARGE BALLOON EXPANDLBE, Nominal Stent Diameter 8 mm, Max Post-Dilated Stent Diameter 16 mm, UDI:
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0018-2022·2021-10-20

    Tone's Taco Seasoning Blend recalled due to undeclared wheat

    B&G Foods North America, Inc. is recalling Tone's Taco Seasoning Blend in plastic bottles because the product contains undeclared wheat, which poses a risk to consumers with wheat allergies.

    Product
    Tone s Taco Seasoning Blend, Plastic Bottles / 12 bottles per case with best by dates of SEPT 03 24 and SEPT 06 24, due to the
    Category
    Food
    Distribution
    44 states
  • HighFDA (Food)·F-0019-2022·2021-10-20

    Brownie Chocolate Walnuts Recalled for Undeclared Walnuts

    Kelly's Bakery Corp. is recalling Brownie Chocolate Walnuts because walnuts are not declared on the product label. Consumers with walnut allergies face a potential allergic reaction.

    Product
    Brownie Chocolate Walnuts, Carton with 96 retail units, A210107B
    Category
    Food
    Distribution
    0 states
  • HighUSDA FSIS·040-2021·2021-10-20

    Mex-tamale Foods Recalls Beef and Pork Tamales for Undeclared Sesame

    Demaiz Inc. is recalling beef and pork tamales sold in Northern California because they contain sesame seeds, an allergen not listed on the label.

    Product
    Demaiz Inc. dba: Mextamale Foods — Demaiz Inc. Recalls Beef And Pork Tamale Products Due To Misbranding And Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0052-2022·2021-10-13

    ZOLL SOLEX 7 Intravascular Catheter Kit Recalled for Potential Leakage

    ZOLL Circulation is recalling 98 units of SOLEX 7 intravascular heat exchange catheter kits due to potential leaks in the catheter or start-up kit tubing. A labeling update has been issued to address the safety concern.

    Product
    Zoll REF: 8700-0793-14 (SL-2593CO), SOLEX 7 Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens), Heparin COATED, Sterile EO, Rx Only, UDI: (01)00849111075541
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0003-2022·2021-10-13

    Medtronic Insertion Kits Recalled for Incorrect Guidewire Label Mix-Up

    Medtronic is recalling 168 Bio-Medicus Insertion Kits because a label mix-up resulted in incorrect guidewires being packaged in both model types. The mislabeling could lead to use of the wrong component during insertion procedures.

    Product
    Medtronic Bio-Medicus Insertion Kits, Model number 96553, Pediatric Insertion Kit, Sterile; and Model number 96551, Venous Insertion Kit, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide