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.

1901–1925 of 9607

  • HighNHTSA·20V530000·2020-09-02

    Utilimaster Metris Recall: Incorrect Payload Labeling May Cause Tire Failure

    Shyft Group is recalling 2020 Utilimaster Metris vehicles because the payload capacity on the Tire and Loading Information label may be higher than the actual capacity, increasing the risk of tire failure and crashes.

    Product
    UTILIMASTER — UTILIMASTER METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1363-2020·2020-09-02

    Organic Valley Egg Bites Recalled for Missing Allergen Labeling

    Almark Foods is recalling Organic Valley Egg Bites because the packaging is missing the back panel with ingredient and allergen information.

    Product
    ORGANIC VALLEY EGG BITES feta & chives NET WT 4 OZ (114g) UPC# 0 93966 81195 7 Distributed by Organic Valley, La Farge, WI 54639
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1540-2020·2020-09-02

    Rocky Mountain Sunscreen Lip Balm Recalled for Excess Octisalate

    Yusef Manufacturing is recalling Rocky Mountain Sunscreen SPF30 Kiwi Flavored Lip Balm because the active ingredient Octisalate was found at 15% above the label claim.

    Product
    Rocky Mountain Sunscreen SPF30 Kiwi Flavored Lip Balm (Oxybenzone 5%, Meradimate 5%, Octinoxate 7.5%, Octisalate 5%) 0.15 Oz Tube, Rocky Mtn. Sunscreen, UPC 7 54018 20004 3
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2849-2020·2020-09-02

    Conformis iTotal Knee Implant Kit Recalled for Incorrect Contents

    Conformis, Inc. is recalling one iTotal CR Knee Replacement kit because the box contained implants and jigs for a different serial number.

    Product
    Conformis iTotal Cruciate Retaining (CR) Knee Replacement System- Orthopedic Implant Cat: TCR-121-1111-010102, (ITOTAL CR IPOLY XE IMPLANT KIT LEFT)
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2889-2020·2020-09-02

    BD SafetyGlide Syringes Recalled for Incorrectly Printed Scale Markings

    Becton Dickinson is recalling 3mL SafetyGlide syringes because the printed scale markings are skewed, missing, or partially printed.

    Product
    BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-2886-2020·2020-09-02

    Match Point System surgical instrument recalled due to incorrect procedure side labeling

    The Match Point System surgical instrument was recalled because the procedure side on planning reports was incorrectly marked as 'Left' instead of 'Right' for right-side procedures.

    Product
    Match Point System The Match Point System is intended to by uses as a surgical instrument to assist in the intraoperative positioning of glenoid components used with total and reverse shoulder arthroplasty by referencing anatomic landmarks of the shoulder that are identifiable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2876-2020·2020-09-02

    OraSure Benzodiazepine Micro-Plate Recall Due to Incorrect Lot Number Labeling

    OraSure Technologies is recalling 39 kits of the Interept Benzodiazepine Micro-Plate EIA due to incorrect lot numbers on the specification sheet and unit box.

    Product
    Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate Matrix Oral Fluid Coated Micro-Plate-IVD Immunoassay for Benzodiazepines, Product Number: 1110IB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2877-2020·2020-09-02

    OraSure Benzodiazepine Micro-Plate Recalled for Incorrect Lot Number Labeling

    OraSure Technologies is recalling 13 kits of Interept Benzodiazepine Micro-Plates due to incorrect lot numbers on specification sheets and unit boxes.

    Product
    Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2 plate Matrix Oral Fluid Coated Micro-Plate. IVD Immunoassay for Benzodiazepines, Product Number: 1110IT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1541-2020·2020-09-02

    Red Cross Oral Pain Relief Recalled for Cotton Pellet Labeling Error

    The Mentholatum Company is recalling Red Cross Oral Pain Relief blister packs because the included cotton pellet box incorrectly lists Natural Eugenol Oil as an ingredient.

    Product
    RED CROSS ORAL PAIN RELIEF — RED CROSS ORAL PAIN RELIEF (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateNHTSA·20V514000·2020-08-27

    2021 BMW X7 Recalled for Incorrect Tire Information Labels

    BMW is recalling 2021 X7 models for tire information labels with incorrect specifications. The labels may not match the actually installed tires, potentially causing drivers to select wrong tires.

    Product
    BMW — BMW X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1167-2020·2020-08-26

    Haven's Kitchen Golden Turmeric Tahini Recalled for Undeclared Soy

    Haven's Kitchen is recalling Golden Turmeric Tahini because the product is labeled as the wrong sauce, resulting in soy being undeclared on the label.

    Product
    HAVEN'S KITCHEN***GOLDEN TURMERIC TAHINI***NET WT 5oz (142g)***Ingredients: Water, Tahini, Extra Virgin Olive Oil, Roasted Garlic, Lemon Juice Concentrate, Date Paste, Sea Salt, Turmeric, Cumin, Ground Sumac (Sumac, Salt), White Pepper***
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1158-2020·2020-08-26

    He Butt Recalls Blue Cheese Salmon Burgers for Undeclared Wheat

    He Butt is recalling specific blue cheese salmon burgers sold in Texas due to undeclared wheat. The recall was initiated voluntarily by the firm.

    Product
    Salmon, Burger Atlantic Blue Cheese Net Weight 12 oz (340g) UPC 23725500000; HEB Meal Simple Blue Cheese Salmon Burger NET WT 12 oz. (340g) UPC 23757500000; HEB Meal Simple Blue Cheese Wild Salmon Burgers NET WT 12oz (340g) UPC 23759000000; Salmon, Burger Atlantic Blue Cheese
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-1508-2020·2020-08-26

    Lannett Recalls Prednisone Tablets Due to Labeling Error

    Lannett Company, Inc. is recalling specific batches of Prednisone Tablets due to a labeling error where 2.5 mg bottles contained 10 mg tablets.

    Product
    Prednisone Tablets, USP 2.5 mg, 100 tablets, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, Manufactured by: Tianjin Tianyao Pharmaceuticals Co., Ltd No. 221 Huanghai Road, Tianjin Economical-Technological Development Area, Tianjin, China 300457 NDC 052
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2828-2020·2020-08-26

    NobelReplace Dental Implant Recall Due to Incorrect Measurement Labeling

    Nobel Biocare is recalling 188 NobelReplace dental implants because the cap label incorrectly lists measurements as 5.0x8mm instead of the actual 4.3x10mm.

    Product
    NobelReplace Conical Connection (CC) PMC RP 4.3x10mm, REF: 37291 - Product Usage: implants are intended to be used in the upper or lower jaw bone (osseointegration) and used for anchoring or supporting tooth replacements to restore chewing function.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1253-2020·2020-08-26

    Woodstock Farms Southwest Tex-Mex Trail Mix Recalled for Undeclared Wheat

    United Natural Trading Inc. is recalling Price Chopper Southwest Tex-Mex Trail Mix because the packaging incorrectly labels the product, failing to declare wheat.

    Product
    Price Chopper, Southwest Tex-Mex Trail Mix, 12 oz. re-closeable bag, 6 packages per case
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2830-2020·2020-08-26

    Pharmaceutical Innovations Recalls Ultra/Phonic Focus BP Conforming Gel Pads

    Pharmaceutical Innovations, Inc. is recalling Ultra/Phonic Focus BP Conforming Gel Pads because the device was incorrectly registered as a Class I device and requires a 510(k) submission.

    Product
    Ultra/Phonic Focus BP Conforming Gel Pads, UDI 00300361301021 (Primary); 10300361301028 (Package) - Product Usage: A gel pad for use on woman s areola during an ultrasound examination. Its primary purpose is for patient comfort over the loose gel and helps with nipple location du
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2806-2020·2020-08-26

    Argon Medical Devices Recalls ClosureFast Micro Introducer Sheath Sets

    Argon Medical Devices is recalling 1,000 units of ClosureFast Micro Introducer Sheath Sets because the sterile products were manufactured under one lot with different expiration dates.

    Product
    ClosureFast Micro Introducer Sheath Set, REF MIS-7F11; 7Fr/Ch (2.3mm)x11 cm. STERILE|EO; Rx ONLY - Product Usage: Introducer Products are stand-alone components, standard kits, or convenience kits built to user specifications. These products facilitate access to a vein or artery,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2813-2020·2020-08-26

    Olympus Recalls Mislabeled Smart Stapes Protheses Piston Medical Devices

    Olympus Corporation of the Americas is recalling 16 units of Smart Stapes Protheses Piston due to outer carton mislabeling.

    Product
    Smart Stapes Protheses Piston 0.4mm X 5.25 mm- Partial Ossicular Replacement Catalog Number: 70142168
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-2814-2020·2020-08-26

    Olympus Smart Stapes Protheses Piston Recalled for Mislabeled Outer Carton

    Olympus is recalling 21 units of Smart Stapes Protheses Piston because the outer carton was mislabeled, potentially containing a different model.

    Product
    Smart Stapes Protheses Piston 0.6mm X 4.25 mm- Partial Ossicular Replacement Catalog Number: 70143662
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-1328-2020·2020-08-19

    San Francisco Street Bakery Recalls Desem Bread for Undeclared Soy

    San Francisco Street Bakery is recalling 14 loaves of Desem Bread because the product contains soy lecithin, which is not declared on the label.

    Product
    Desem Bread, San Francisco Street Bakery brand, keep at ambient temperature. Individually packaged in flex poly bag, net weight 22 oz. UPC 0 08613 10001 8. The product label read: "***desem ***Ingredients: stone ground organic whole wheat flour, water, organic wheat flour, so
    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-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-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-1153-2020·2020-08-19

    Sweeteeth Chocolate Bar Recalled for Unlabeled Soy Allergen

    Sweeteeth Chocolate LLC is recalling White Chocolate & Ginger Snaps bars because they contain soy, which is not listed on the label.

    Product
    Sweeteeth O-Snap! (White Chocolate & Ginger Snaps) Chocolate Bar, NET WT. 3 OZ. (85.05G), Manufactured by: Sweeteeth Chocolate LLC. 1204 McNew St. Hanahan, SC 29410 www.evopizza.com, Best By: 07/28/2021, UPC 7 36211 11895 0
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1332-2020·2020-08-19

    San Francisco Street Bakery Recalls Pain Au Levain Bread for Undeclared Soy

    San Francisco Street Bakery Inc. is recalling 62 loaves of Pain Au Levain Bread because the product contains soy lecithin, which is not declared on the label.

    Product
    Pain Au Levain Bread, San Francisco Street Bakery brand, keep at ambient temperature. Individually packaged in flex poly bag, net weight 16 oz (454 g). UPC 0 08613 10013 1. The product label is read in parts: "***Pain Au Levain Bread ***Ingredients: unbleached wheat flour, wa
    Category
    Food
    Distribution
    1 state