The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 mis labeling recalls we have scored against our rubric, 161 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 589 (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.

6576–6600 of 9611

  • HighFDA (Food)·F-1870-2015·2015-04-08

    Mrs. Fields Macadamia Cookies Recalled for Allergen Labeling Error

    Interbake Foods is recalling Mrs. Fields White Chunk Macadamia Cookies because the packaging failed to declare the presence of the macadamia allergen as required by FALCPA.

    Product
    Mrs. Fields White Chunk Macadamia Cookies; 12 individually wrapped cookies in a tray/box; there are 6 trays/boxes to a case. Therefore there are 72 cookies in a case; 2.1 oz single size serving.
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1875-2015·2015-04-08

    Michael Foods Recalls Frozen Egg Patties Due to Undeclared Milk Allergen

    Michael Foods is recalling 181,127 cases of frozen egg patties because they contain milk, an allergen not declared on the label.

    Product
    Natural Shaped Fried Egg (patties), 1.75 oz. frozen egg patties, packaged 144-count per case, Net WT. 15.75 lb. (7.14 KG), under two brand names: (1) Pappetti's Table Ready, UPC Code 46025 85879. The responsible firm name on the label is Michael Foods Inc., Minnetonka, MN 553
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1338-2015·2015-04-08

    Microtek Medical Recalls Surgical Helmet Motor Modules for Latex Packaging

    Microtek Medical Inc is recalling 38 units of FREEDOMAIRE Motor Modules because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) MOTOR MODULE, REF 11112STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical personnel in order to protect against contamination, body fl
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1342-2015·2015-04-08

    Microtek Smoke Evacuation Tubing Set Recalled for Latex Packaging Labeling Error

    Microtek Medical Inc is recalling 303 Smoke Evacuation Tubing Sets because the packaging contains latex but lacks the required warning label.

    Product
    Smoke Evacuation Tubing Set for Coherent CPG Handpiece, 7/8" x 16' (2.22 cm x 487.88 cm), REF 24244, QTY 3/CS, NON STERILE NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool sur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1349-2015·2015-04-08

    Microtek Medical recalls sterile smoke evacuator wands due to latex packaging

    Microtek Medical is recalling sterile smoke evacuator wands because the packaging contains latex but lacks the required warning label.

    Product
    INTEGRAL WAND W/TUBING, STERILE, REF 24185, QTY 24/CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms, Trauma, Endosc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1783-2015·2015-04-08

    ProSupps Recalls MR. Hyde Pre-Workout for Undeclared Yohimbine Levels

    ProSupps USA LLC is recalling MR. Hyde Intense Energy Pre Workout because it contains more yohimbine HCL than declared on the label.

    Product
    MR. HYDE INTENSE ENERGY PRE WORKOUT, Green Apple Natural and Artificial Flavor Dietary Supplement Net Weight 8.0 OZ (228 grams)
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1340-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmets Due to Latex Packaging

    Microtek Medical Inc is recalling 11 units of Freedomaire Surgical Helmet Systems because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET SYSTEM WITH BELT, REF 11114STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical personnel in order to protect against contaminati
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1339-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmets Due to Latex Packaging

    Microtek Medical Inc is recalling 153 Freedomaire Surgical Helmets because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET WITH MOTOR MODULE, REF 11113STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical personnel in order to protect against contaminat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1347-2015·2015-04-08

    Microtek Medical Smoke Evacuator Tube Sets Recalled for Latex Packaging

    Microtek Medical Inc is recalling sterile smoke evacuator tube sets because the packaging contains latex without the required warning label.

    Product
    (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor, Sterile, REF 24155, QTY 10/CS, STERILE EO, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical p
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1368-2015·2015-04-08

    Quest Medical Recalls Lacrimal Intubation Sets Due to Labeling Error

    Quest Medical is recalling 106 units of LIS27T Lacrimal Intubation Sets because the expiration date was incorrectly printed in the manufacturing date field.

    Product
    LIS27T - Lacrimal Intubation Set RX Only Sterile Used in various ophthalmology procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1348-2015·2015-04-08

    Microtek Medical Recalls Sterile Laser Resistant Wands Due to Latex Packaging

    Microtek Medical Inc is recalling sterile laser resistant wands because the packaging contains latex but lacks the required warning label.

    Product
    LASER RESISTANT WAND - STERILE, 7/8" X 8" (2.22cm x 20.32cm), REF 24013, QTY 10 EA, STERILE EO, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Location
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1337-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmet Systems Due to Latex Packaging

    Microtek Medical is recalling 10 Freedomaire Surgical Helmet Systems because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY, LUMBAR BELT AND MOTOR MODULE, REF 11110STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1345-2015·2015-04-08

    Microtek Medical Recalls Sterile Vacuum Tubing Due to Unlabeled Latex Packaging

    Microtek Medical Inc is recalling sterile vacuum tubing because the packaging contains latex but lacks the required warning label.

    Product
    VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm), WITH TUBING EXTENDER, STERILE, REF 24010, QTY 24\CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locati
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1372-2015·2015-04-08

    Biologic Therapies Recalls Bio-PLASTY Cannulas for Misbranding

    Biologic Therapies, Inc. is recalling 58 Bio-PLASTY Cannulas because they were distributed without proper FDA clearance and classification.

    Product
    Bio-PLASTY Cannula (Needle)
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1374-2015·2015-04-08

    Biologic Therapies Recalls Bio-CORE Cannula Sets for Misbranding

    Biologic Therapies, Inc. is recalling Bio-CORE Cannula (Needle) Sets because they were distributed without proper FDA clearance and classification.

    Product
    Bio-CORE Cannula (Needle) Set
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1361-2015·2015-04-08

    King Systems Double Swivel Connector Recalled for Mislabeling

    King Systems Corp. is recalling 900 units of Double Swivel Connectors mislabeled as having a suction port. The error may cause a short procedure delay but poses no risk to patients.

    Product
    Double Swivel Connector with Suction Port Connector, Airway (Extension) King Systems part 7169 Product Usage: An airway connector is a device intended to connect a breathing gas source to a tracheal tube, tracheostomy tube, or gas mask. The double swivel connector with suct
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1343-2015·2015-04-08

    Microtek Medical Smoke Evacuator Tubing Recalled for Unlabeled Latex Packaging

    Microtek Medical is recalling smoke evacuator tubing because the packaging contains latex but lacks the required warning label.

    Product
    TUBING 7/8' X 10', W/WAND & TIP, 24/CS, REF 24187, QTY 24\CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms, Trauma,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1344-2015·2015-04-08

    Microtek Medical Recalls Vacuum Tubing Due to Unlabeled Latex Packaging

    Microtek Medical Inc is recalling non-sterile vacuum tubing because the packaging contains latex but lacks the required warning label.

    Product
    VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm), REF 24009, QTY 24\CS, NON-STERILE Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms, T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1617-2015·2015-04-01

    FGF Brands Recalls Mini Naan for Missing Allergen and Nutrition Labels

    FGF Brands, Inc. is recalling 7,783 cases of Mini Naan because the packages were shipped without labels declaring ingredients, nutrition, or allergens.

    Product
    Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360 g) per package and old under the US Foods brand. Product is labeled with instructions to keep frozen until use. Eight (8) packages per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1573-2015·2015-04-01

    Vitony Bakery Recalls Guava Pastries Due to Missing Soy Labeling

    Vitony Bakery, Inc. is recalling 204 units of guava-filled pastries in Puerto Rico because the ingredient label fails to list soy lecithin.

    Product
    Guava filled pastry ("Pastelillo de Guayaba" in Spanish) 2.5 oz and 10 oz.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1313-2015·2015-04-01

    Synthes Electric Pen Drive Hand Switch Labeling Error Recall

    Synthes, Inc. is recalling 249 Electric Pen Drive systems because the Hand Switch labels for 'on' and 'lock' were interchanged.

    Product
    Synthes Electric Pen Drive (EPD) System, The Synthes Electric Pen Drive is indicated for screw insertion, pin and wire replacement, cutting of bone and metal, drilling, decorticating, shaping, and smoothing of bones and teeth in a wide variety of surgical procedures, including, b
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1321-2015·2015-04-01

    Siemens ADVIA Chemistry Systems Drug Calibrator I Recalled for Incorrect Values

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Systems Drug Calibrator I, lot 3JD018, due to incorrect calibrator values for Phenytoin 2 and Phenobarbital 2 assays.

    Product
    ADVIA Chemistry Systems Drug Calibrator I; For in vitro diagnostic use in the calibration of Phenobarbital_2 (PHNB_2), Phenytoin_2 (PHNY_2), and Theophylline_2 (THEO_2) methods on the ADVIA Chemistry systems. System Information: (For Information Only) The ADVIA Chemistry system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1325-2015·2015-04-01

    Zimmer NexGen Trabecular Metal Femoral Augment Block Mislabeled Recall

    Zimmer Trabecular Metal Technology is recalling one unit of a NexGen femoral augment block that was mislabeled as 5 mm instead of 20 mm.

    Product
    NexGen TRABECULAR METAL FEMORAL AUGMENT BLOCK DISTAL ONLY, 20 MM Augment, Size D, Sterile, Rx Only. Product Usage: Intended for use where severe degeneration, trauma, or other pathology of the knee joint indicates total knee arthroplasty. When used with the NexGen Complete Kn
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1615-2015·2015-04-01

    Sunshine Organic Veggie Burgers Recalled for Gluten Contamination

    Sunshine Burger & Specialty Food Company is recalling frozen veggie burgers labeled gluten-free because testing found gluten levels above 20 ppm.

    Product
    Frozen vegetable-based burgers RETAIL - DOMESTIC: Organic Sunshine Burgers Gluten Free Soy Free Vegan South West 3 Organic Veggie Burgers Keep Frozen Net WT: 8 OZ. Use By: 7/13/16; 7/21/16; 7/28/16; 8/4/16; 8/11/16; FOOD SERVICE: Sunshine Southwestern Style Veggie B
    Category
    Food
    Distribution
    9 states