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.

1926–1950 of 9607

  • HighFDA (Food)·F-1155-2020·2020-08-19

    Marketside Peanut Butter Brownies Recalled for Missing Allergen Labeling

    James Skinner Baking Co. is recalling Marketside Peanut Butter Brownies because units may lack the ingredient list, failing to declare major allergens including peanuts, wheat, milk, egg, and soy.

    Product
    Marketside Peanut Butter Brownie, Net Wt. 19 oz, Distributed by Walmart Inc. Bentonville, AR
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1333-2020·2020-08-19

    San Francisco Street Bakery Recalls Rosemary Garlic French Bread for Undeclared Soy

    San Francisco Street Bakery is recalling 36 units of Rosemary Garlic French Bread because the product contains soy lecithin, which is not declared on the label.

    Product
    Rosemary Garlic French Bread, San Francisco Street Bakery brand, keep at ambient temperature. Individually packaged in flex poly bag, net weight 14 oz (400 g). UPC 0 08613 10008 7. The product label is read in parts: "***Rosemary Garlic French Bread***Ingredients: Unbleached
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1319-2020·2020-08-19

    San Francisco Street Bakery Recalls Cinnamon Raisin Bagels for Undeclared Soy

    San Francisco Street Bakery is recalling Cinnamon Raisin Bagels because they contain soy lecithin, which is not declared on the label.

    Product
    Cinnamon Raisin Bagel, San Francisco Street Bakery brand, keep at ambient temperature. Packaged in flex poly bags for bulk or various quantities specific to customer order. No UPC. The bagel bulk product label read: CINNAMON RAISIN BAGELS: Bread Flour (Unbleached Wheat Flour,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1325-2020·2020-08-19

    San Francisco Street Bakery Recalls Poppy Seed Bagels Due to Soy Allergen

    San Francisco Street Bakery is recalling Poppy Seed Bagels because they were treated with a pan release spray containing soy lecithin, which is not declared on the label.

    Product
    Poppy Seed Bagel, San Francisco Street Bakery brand, keep at ambient temperature. Packaged in flex poly bags for bulk or various quantities specific to customer order. No UPC. The bagel bulk product label read: POPPY SEED BAGEL: Bread Flour (Unbleached Wheat Flour, Vitamin C,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1330-2020·2020-08-19

    San Francisco Street Bakery Recalls Italian Farm Bread for Undeclared Soy

    San Francisco Street Bakery is recalling 34 loaves of Italian Farm Bread because the product contains soy lecithin, which is not declared on the label.

    Product
    Italian Farm Bread, San Francisco Street Bakery brand, keep at ambient temperature. Individually packaged in flex poly bag, net weight 23 oz (652 g). UPC 0 08613 10005 6. The product label is read in parts: "***Italian Farm Bread ***Ingredients: unbleached wheat flour, cracke
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1322-2020·2020-08-19

    San Francisco Street Bakery Onion Bagels Recalled for Undeclared Soy

    San Francisco Street Bakery is recalling Onion Bagels because they contain soy lecithin, an ingredient not listed on the product label.

    Product
    Onion Bagel, San Francisco Street Bakery brand, keep at ambient temperature. Packaged in flex poly bags for bulk or various quantities specific to customer order. No UPC. The bagel bulk product label read: ONION BAGEL: Bread Flour (Unbleached Wheat Flour, Vitamin C, Niacin, R
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1327-2020·2020-08-19

    San Francisco Street Bakery Recalls Sesame Seed Bagels Due to Undeclared Soy

    San Francisco Street Bakery is recalling Sesame Seed Bagels because the product contains soy lecithin, which is not declared on the label.

    Product
    Sesame Seed Bagel, San Francisco Street Bakery brand, keep at ambient temperature. Packaged in flex poly bags for bulk or various quantities specific to customer order. No UPC. The bagel bulk product label read: SESAME SEED BAGEL: Bread Flour (Unbleached Wheat Flour, Vitamin
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1321-2020·2020-08-19

    San Francisco Street Bakery Garlic Bagels Recalled for Undeclared Soy

    San Francisco Street Bakery is recalling Garlic Bagels produced in July 2020 because they contain soy lecithin, an ingredient not listed on the label.

    Product
    Garlic Bagel, San Francisco Street Bakery brand, keep at ambient temperature. Packaged in flex poly bags for bulk or various quantities specific to customer order. No UPC. The bagel bulk product label read: GARLIC BAGEL: Bread Flour (Unbleached Wheat Flour, Vitamin C, Niacin,
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2798-2020·2020-08-19

    FDA Recalls Barricaid Annual Closure Devices Due to Labeling Error

    Intrinsic Therapeutics is recalling 110 units of Barricaid Annual Closure Devices because the inner container labels display the wrong catalog number.

    Product
    Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The Barricaid¿ ACD is indicated for reducing the incidence of reherniation, and reoperation in skeletally mature patients with radiculopathy (with or without back pain) attributed to a posterior or posterolateral h
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2803-2020·2020-08-19

    Arrow TheraCath Epidural Catheter Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling TheraCath Epidural Catheters because the lidstock displays an incorrect expiration date, potentially leading to the use of expired devices.

    Product
    Arrow TheraCath Epidural Catheter - Product Usage: The Arrow Epidural Catheter permits access to the epidural space.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2777-2020·2020-08-19

    Smith & Nephew Recalls Misidentified PeriLoc Targeter Handle

    Smith & Nephew is recalling 3 units of a PeriLoc Targeter handle that was incorrectly marked as a left-hand part.

    Product
    PERI-LOC TARGETER 4.5MM DISTAL FEMUR, HANDLE, LEFT, NON-STERILE - Product Usage: used for adult and pediatric patients, as well as patients with osteopenic bone. PERI-LOC plates and screws are indicated for fixation of pelvic, small and long bone fractures, including those of the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2802-2020·2020-08-19

    Arrow International Recalls Cannon II Plus Replacement Hub Sets for Labeling Error

    Arrow International Inc is recalling Cannon II Plus Replacement Hub Sets because the lidstock displays an incorrect expiration date, which could lead to the use of expired devices.

    Product
    Cannon II Plus Replacement Hub Set - Product Usage: is indicated for use in the replacement of a Cannon II Plus hub connection assembly that has been damaged.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2790-2020·2020-08-19

    HF Acquisition Recalls STAT KIT 550 Emergency Medical Kits

    HF Acquisition Co., LLC is recalling 155 STAT KIT Model 550 Emergency Medical Kits because they contain one dose of Narcan Nasal spray instead of two.

    Product
    STAT KIT Model 550 Emergency Medical Kit P/N: 1009580 containing various products to include Narcan Nasal spray, item number 1010300
    Category
    Medical Device
    Distribution
    39 states
  • ModerateFDA (Drugs)·D-1492-2020·2020-08-19

    Teva Recalls Lidocaine Patches Due to Missing Lot and Expiration Dates

    Teva Pharmaceuticals is recalling Lidocaine 5% Patches because individual pouches are missing lot and expiration dates. The recall covers 28,596 cartons distributed nationwide.

    Product
    LIDOCAINE — LIDOCAINE (LIDOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2804-2020·2020-08-19

    Arrow International Recalls NextStep Retrograde Replacement Hub Set Due to Labeling Error

    Arrow International is recalling NextStep Retrograde Replacement Hub Sets because the lidstock displays an incorrect expiration date, which could lead to the use of expired devices.

    Product
    NextStep Retrograde Replacement Hub Set - Product Usage: is indicated for use in the replacement of a NextStep Retrograde hub connection assembly that has been damaged.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2801-2020·2020-08-19

    Arrow Single Shot Epidural Anesthesia Kit Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling specific lots of Single Shot Epidural Anesthesia Kits because the lidstock displays an incorrect expiration date, which could lead to the use of expired devices.

    Product
    Arrow Single Shot Epidural Anesthesia Kit - Product Usage: The Arrow Blunt Needle Single Shot Epidural Kit permits access to the epidural space.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-2781-2020·2020-08-19

    Linet AVE 2 Birthing Bed Recalled for Incorrect Manufacturer Labeling

    Linet Americas is recalling 202 AVE 2 Birthing Beds because the Unique Device Identifier (UDI) on the label indicates the incorrect manufacturer.

    Product
    AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also as aid to search for individual positions providing relief in all delivery stages including postpartum period. Birthing bed is not intended for use as a general
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2744-2020·2020-08-12

    Sutter Swyng Non-Stick Bipolar Forceps Recalled for Incorrect Package Insert Labeling

    Sutter Medizintechnik GmbH is recalling 1,337 units of Sutter Swyng non-stick bipolar forceps because the package insert incorrectly displays the Ethylene Oxide sterilization symbol instead of the irradiation symbol.

    Product
    Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps are provided with bayonet-style handle design with straight or angled tips and different total lengths. They are to be connected through an appropriate bipolar
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1044-2020·2020-08-05

    Kasugai Matcha Ame Candy Recalled for Undeclared Soybean Allergen

    J F C International Inc is recalling Kasugai brand Matcha Ame candy because the label fails to declare soybean, a major food allergen, present in the mold lubricant.

    Product
    Kasugai brand Matcha Ame (Green tea candy); 4.58 oz. plastic bag; 2 x 12 individual items per case Product of Japan Ingredients: glucose syrup, sugar, green tea powder, palm oil, artificial flavor. The label should include "mold lubricant oil (palm, rapseed, soybeans)
    Category
    Food
    Distribution
    25 states
  • HighFDA (Food)·F-1032-2020·2020-08-05

    Happy Colon Yum Shortbread Cookie Recalled for Undeclared Milk

    Happy Colon Foods is recalling Yum Shortbread Cookies because they contain butter but do not list milk as an ingredient.

    Product
    Happy Colon Yum Shortbread Cookie 0.98oz UPC 56817 00704
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1033-2020·2020-08-05

    Happy Colon Chocolate Chip Cookies Recalled for Undeclared Milk

    Happy Colon Foods is recalling specific chocolate chip cookies because they contain butter but do not list milk as an ingredient.

    Product
    Happy Colon MMMM Chocolate Chip Cookie 0.98oz UPC 56817 00703
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1047-2020·2020-08-05

    Stick-E Fingers Barbecue Rub Recalled for Undeclared Milk Allergen

    Stick E Fingers BBQ LLC is recalling 181 jars of All Purpose Rub because the label declares butter but fails to list milk or buttermilk.

    Product
    Stick-E Fingers Barbecue All Purpose Rub is a dry rub, packaged in 13.2 oz plastic jar, UPC 8 60003 24004 5. No company's address listed on the label. The product label is read in parts: "***STICK-E FINGERS BARBECUE***All Purpose Rub *** INGREDIENTS: SALT, ONION, BUTTER FLAVO
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2739-2020·2020-08-05

    Synthes Recalls MatrixMIDFACE Screws Due to Incorrect Size Marking

    Synthes Produktions GmbH is recalling 41 units of MatrixMIDFACE Screws because the body clip was etched with the wrong size number.

    Product
    MatrixMIDFACE Screws - Product Usage: The intended use for this device is in fixation of cranial bones and facial skeleton in procedures such as craniotomies, reconstructive procedures, fracture repair, osteotomies, and selective orthognathic surgery of the maxilla and chin.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1423-2020·2020-08-05

    MasterPharm Recalls Formula 82F Minoxidil Tretinoin Fluocinolone Acetonide Finasteride

    MasterPharm LLC is recalling 462 units of Formula 82F topical solution due to a lack of processing controls that compromised product specifications.

    Product
    Formula 82F (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone Acetonide 0.01%/Finasteride 0.25%), 0.5 FL OZ (15 mL) bottle MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600.
    Category
    Drug
    Distribution
    Distributed nationwide