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.

126–150 of 9606

  • LowFDA (Drugs)·D-0343-2026·2026-03-04

    Eptifibatide Injection Labeling Error Recall by Slate Run

    Slate Run Pharmaceuticals is recalling Eptifibatide Injection due to a labeling error on the carton, which incorrectly describes the dosing instructions.

    Product
    EPTIFIBATIDE — EPTIFIBATIDE (EPTIFIBATIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·26305·2026-02-26

    SumDirect LED Mini Lights Recalled Over Battery Ingestion Hazard

    SumDirect LED Mini Lights are recalled because the button cell batteries can be easily accessed by children, posing an ingestion hazard. No injuries have been reported.

    Product
    SumDirect LED Mini Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1427-2026·2026-02-25

    Stryker MOLLI 2 System Recall: Marker Dislodgement Risk

    Stryker is recalling the MOLLI 2 System due to magnetized surgical tools that may dislodge markers during target tissue removal procedures. The recall affects 5,864 units distributed worldwide.

    Product
    MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195028 MS-00009 (Pack of 10) - MOLLI Introducer (12cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195134 MP2001 - MOLLI 2 Wand UDI (GTIN): 008500241951
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V033000·2026-01-22

    Blue Bird Recalls One 2026 Vision Transit Bus for Window Markings

    Blue Bird is recalling one 2026 Vision transit bus because side or rear windows may have illegible DOT markings, failing federal safety standards.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V032000·2026-01-22

    Blue Bird Recalls 2026-2027 School Buses for Illegible Window Markings

    Blue Bird is recalling 2026-2027 Vision and All American school buses because side and rear windows may have illegible DOT markings, failing federal safety standards.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26E004000·2026-01-16

    Lippert Recalls Bus Windows with Illegible DOT Markings

    Lippert is recalling certain bus windows that may have illegible DOT markings, failing to comply with Federal Motor Vehicle Safety Standard 205.

    Product
    VISIBILITY:GLASS, SIDE/REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V005000·2026-01-09

    Land Rover Recalls 2026 Range Rover Sport for Incorrect Weight Label

    Jaguar Land Rover is recalling 2026 Range Rover Sport vehicles because the certification label lists incorrect weight information, which could lead to overloading.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·038-2025·2025-12-12

    Suzanna's Kitchen Recalls Breaded Chicken for Undeclared Soy Allergen

    Suzanna's Kitchen is recalling fully cooked breaded chicken products because they contain soy, a known allergen, that is not declared on the label.

    Product
    Suzanna's Kitchen — Suzanna’s Kitchen Recalls Fully Cooked Breaded Chicken Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·25V847000·2025-12-09

    Jayco Recalls 2025-2026 Melbourne and Entegra Qwest RVs for Weight Label Errors

    Jayco is recalling specific 2025-2026 recreational vehicles because incorrect weight ratings on labels may lead to unintentional overloading and increased crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO QWEST, MELBOURNE PRESTIGE, MELBOURNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V814000·2025-11-24

    nuCamp Trailers Recalled for Incorrect Weight Labels

    Pleasant Valley is recalling 2025-2026 nuCamp trailers because incorrect weight information on labels may lead to unintentional overloading and increased crash risk.

    Product
    NUCAMP — NUCAMP TAG, TAB 400, TAB 360, TAB 320
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V790000·2025-11-17

    Triple E Recalls 2025-2026 Unity RVs Due to Incorrect Seat Belt Labeling

    Triple E is recalling 2025-2026 Unity recreational vehicles because the weight label incorrectly lists a seating capacity of four, while the vehicle is equipped with only two seat belts.

    Product
    TRIPLE E — TRIPLE E UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V701000·2025-10-15

    Winnebago Recalls Travel Trailers Due to Incorrect Federal Tire Labeling

    Winnebago is recalling specific travel trailers because the Federal tire label may list the incorrect tire size, creating a risk of installing the wrong tire.

    Product
    WINNEBAGO — WINNEBAGO MINNIE PLUS5, MINNIE, MINNIE DROP, HIKE100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2618-2025·2025-10-01

    Extractor Pro RX Retrieval Balloon Catheter incorrectly labeled

    Boston Scientific Corporation is recalling Extractor Pro RX Retrieval Balloon Catheters because the label incorrectly indicates the position of the skive hole relative to the balloon.

    Product
    Extractor Pro RX Retrieval Balloon Catheter; UPN (REF): (1) M00547030 (9-12mm Below), (2) M00547000 (9-12mm Above);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V578000·2025-09-04

    Jayco Recalls 2026 Seismic Fifth Wheels for Incorrect Weight Labels

    Jayco is recalling 2026 Seismic fifth wheel travel trailers because the certification label lists an incorrect Gross Axle Weight Rating (GAWR).

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E051000·2025-08-25

    Truck Certification Services Recalls Load Carrying Capacity Labels

    Truck Certification Services is recalling specific Load Carrying Capacity labels where weight units may be reversed, potentially leading to vehicle overloading.

    Product
    EQUIPMENT:OTHER:LABELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-07302025-01·2025-07-30

    Frozen Pork and Beef Tortellini Recalled for Undeclared Soy and Sesame Allergens

    USDA FSIS issued a public health alert for frozen tortellini that may contain undeclared soy and sesame. Consumers with allergies should not consume the product.

    Product
    P.E. & F Inc. DBA DiMare's Specialty Foods — FSIS Issues Public Health Alert for Frozen Pork and Beef Tortellini Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    4 states
  • HighUSDA FSIS·PHA-07112025-01·2025-07-11

    USDA Issues Alert for Pulled Pork Products with Undeclared Allergens

    USDA FSIS issued a public health alert for Roth Premium Foods pulled pork products due to misbranding and undeclared allergens, including soy, fish, and egg.

    Product
    Roth Premium Foods, LLC — FSIS Issues Public Health Alert for Ready-To-Eat Pulled Pork Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2076-2025·2025-07-09

    Bard Urologist's Tray Recalled Over Incorrect French Size Labeling

    C.R. Bard Inc is recalling 63 units of the Bard Urologist's Tray due to cather packaging that may contain the incorrect French size, which could affect device use.

    Product
    REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2075-2025·2025-07-09

    BD Heyman Coude Tip Catheters Recalled Over French Size Labeling Error

    C.R. Bard Inc is recalling certain BD Heyman Follower Coude Tip catheters because the packaging may display the incorrect French size, which could lead to use of the wrong size device.

    Product
    BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr - REF:021314, 16Fr - REF: 021316
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0065-2025·2025-07-02

    Firehook Artisan Baked Crackers Recalled for Undeclared Sesame

    Firehook of Virginia is recalling Firehook Artisan Baked Crackers Classic Sea Salt because some packages contain Everything Bagel Crackers, which include sesame that is not listed on the label.

    Product
    FIREHOOK ARTISAN BAKED CRACKERS CLASSIC SEA SALT NET WT. 8 OZ (227g) INGREDIENTS: ORGANIC WHEAT FLOUR, ORGANIC HONEY, YEAST, SALT, ORGANIC OLIVE OIL, CONTAINS: WHEAT UPC 8 99055 00063 5 FIREHOOK OF VIRGINIA, INC. CHANTILLY, VA 20151
    Category
    Food
    Distribution
    11 states