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.

4626–4650 of 9607

  • HighFDA (Food)·F-2154-2017·2017-05-24

    Raley's Muesli Red Berry Crunch Cereal Recalled for Missing Coconut Allergen

    Raley's is recalling Muesli Red Berry Crunch Cereal because an internal review found coconut was not listed in the allergen declaration.

    Product
    RALEY'S MUESLI RED BERRY CRUNCH CEREAL; 12 oz. box - foil bag inside paper box. UPC: 46567-02264;product Distributed by Raley's, West Sacramento, CA;Product of Switzerland
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-2239-2017·2017-05-24

    Herbalife Recalls Peanut Butter Protein Bars Due to Fish Gelatin

    Herbalife is recalling Peanut Butter Protein Bars because they may contain trace amounts of fish gelatin, an undeclared allergen.

    Product
    Protein Bar 14 bars/box, Net Wt. 19.74oz (560g) Each shipping carton contains 12 boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2073-2017·2017-05-24

    Biomet Microfixation Recalls Surgical Trays Due to Part Number Mismatch

    Biomet Microfixation is recalling 33 TraumaOne System Surgical Trays because the part number on the lid differs from the base.

    Product
    Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1893-2017·2017-05-24

    Ziehm Imaging solo FD Mobile Fluoroscopic C-arm Recalled for Missing Label Date

    Ziehm Imaging Inc is recalling two solo FD Mobile Fluoroscopic C-arm systems because the labels for the Collimator and X-ray Control panel are missing the manufacturer date.

    Product
    Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2108-2017·2017-05-24

    Teleflex Recalls Visistat Skin Staplers Due to Labeling Error

    Teleflex Medical is recalling Visistat 35R Disposable Skin Staplers because some boxes are mislabeled as containing Wide devices when they contain Regular devices.

    Product
    WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin closure of lacerations on the outer layer of the dermis for a wide range of general, thoracic, obstetric, gynecological, orthopedic, cardiovascular, urologic
    Category
    Medical Device
    Distribution
    20 states
  • LowFDA (Devices)·Z-2116-2017·2017-05-24

    Medtest Holdings Recalls Pointe Scientific Hitachi AST Reagent Due to Labeling Discrepancy

    Medtest Holdings is recalling Pointe Scientific Hitachi AST Reagent because the package insert contains inconsistent linearity values in different sections.

    Product
    Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle w/PP plastic cap. R2: PE plastic bottle w /PP plastic cap. Product Usage: Two Part Chemistry Reagent For the quantitative determination of Aspartate Aminotransferase (ASl) in human serum on Hitachi analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowNHTSA·17V327000·2017-05-18

    BMW Recalls 2017 X5 M and X6 M for Incorrect Tire Labeling

    BMW is recalling 2017 X5 M and X6 M vehicles because the tire information label lists the wrong tire size, failing to meet federal safety standards.

    Product
    BMW — BMW X5, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2203-2017·2017-05-17

    Reser's Macaroni Salad Recalled for Undeclared Milk and Soy Allergens

    Reser's Fine Foods is recalling American Classics Macaroni Salad because it contains undeclared milk and soy. The product was distributed to wholesalers in 12 states.

    Product
    Reser's Fine Foods, American Classics Macaroni Salad, Net Wt 1 lb. (454 g) UPC 7117.19007, packaged in 16 oz plastic tubs, 12 per case. Reser's Fine Foods, Inc. Beaverton, OR 97006.
    Category
    Food
    Distribution
    12 states
  • HighNHTSA·17V325000·2017-05-17

    Bison Horse Trailers Recalled for Incorrect Weight Rating Labels

    Bison Coach is recalling 2016-2018 horse trailers due to incorrect Gross Axle Weight Rating labels, which may lead to overloading and increased crash risk.

    Product
    BISON — BISON LAREDO, TRAIL HAND, TRAIL BOSS, SILVERADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2185-2017·2017-05-17

    Unisea Recalls Frozen Wild Shrimp Burgers Due to Allergen Labeling Error

    Unisea Inc. is recalling Wild Grill Foods brand frozen shrimp burgers because the packaging failed to list butter as an ingredient in the allergen declaration.

    Product
    Frozen Wild Shrimp Burgers, Wild Grill Foods brand, net wt. 12 oz. Each package contains 4/ 3 oz. pieces. UPC 8 94067 00248 6. The 12 oz. package label is read in parts: "***SHRIMP BURGERS***WILD GRILL***Net WT WT. 12 OZ.***Distributed by Wild Grill Foods***INGREDIENTS: Shrim
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-2059-2017·2017-05-17

    Zimmer Biomet Recalls Mislabeled Bone Dowell Harvest Tubes

    Zimmer Biomet is recalling 49 Bone Dowell Harvest Tubes that were mislabeled as 8mm but are actually 9mm in size.

    Product
    Bone Dowell Harvest Tubes
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2071-2017·2017-05-17

    Stryker PROFESS Registration Kit Recalled for Expiration Date Issues

    Stryker is recalling 65 PROFESS Registration Kits shipped near or past their expiration dates. The kits are used for intranasal and sinus surgery.

    Product
    Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guidance system to enable intranasal and sinus computer-assisted surgery. The system is comprised of PROFESS Registration Stickers, a P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2208-2017·2017-05-17

    Vertical Pharmaceuticals Recalls OB Complete Prenatal Multivitamin Due to Labeling Error

    Vertical Pharmaceuticals is recalling one lot of OB Complete with DHA Prenatal Multivitamin because the label claim for Omega-3 Fatty Acids does not match the actual formulation.

    Product
    Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical Pharmaceuticals, LLC Sayreville, NJ 08872 UPC 368025049603
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-2054-2017·2017-05-17

    CooperSurgical lnflatoball Pessary Recalled for Incorrect Latex-Free Labeling

    CooperSurgical is recalling lnflatoball Latex Rubber Pessaries because the secondary packaging incorrectly states the product is latex-free, despite being made of 100% latex.

    Product
    CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary Kit. Product Usage: The lnflatoball Pessary is a single-patient use pessary manufactured from natural latex rubber and is used for treating cystocele and/or rec
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2036-2017·2017-05-17

    Smith & Nephew Recalls Mislabelled Peri-Loc Volar Distal Radius Plates

    Smith & Nephew is recalling 12 units of Peri-Loc Volar Distal Radius plates that were laser-etched as left plates but packaged as right plates.

    Product
    PERI-LOC VOLAR DISTAL RADIUS - RIGHT 3H STD HEAD LOCKING PLATE, 62 MM LENGTH, SST PLATE, REF 71823114, QTY: (1) NON-STERILE, Rx only, Smith & nephew, Inc., Memphis TN 38116
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2069-2017·2017-05-17

    Almore Microfil Composite Instruments Recalled for Incorrect Sterile Labeling

    Almore International Inc. is recalling Microfil Composite Instruments because packaging labels incorrectly display a sterile symbol, although the devices are not sterile.

    Product
    Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box. Microfil Composite Instruments are intended to be sterilized by the dentist prior to each use. It is used for composite restoration development. The thin paddles
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2047-2017·2017-05-17

    Medtronic PAK Needle Beveled and Trocar Tips Recalled for Packaging Error

    Medtronic is recalling 36 units of PAK Needle Beveled and Trocar Tips because packaging may contain incorrect needle types instead of the required combination.

    Product
    Medtronic PAK NEEDLE BEVELED AND TROCAR TIPS, REF 8670009, QTY 1 EA, STERILE R, Rx only
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Food)·F-2175-2017·2017-05-10

    Killer Brownie Recalls Brownies for Undeclared Peanuts

    Killer Brownie Distributing LLC is recalling Original KB Killer Brownies due to undeclared peanuts. The product was distributed to Minnesota, New York, Ohio, Pennsylvania, and Wisconsin.

    Product
    ORIGINAL KB KILLER BROWNIE¿ 3x35 CT NET WT 36 LBS (16.33 kg) CONTAINS: Milk, Nuts: Pecans, Soy, Wheat UPC 10858061005031. Item #48-2016
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-2174-2017·2017-05-10

    Killer Brownie Distributing Recalls Brownies Due to Undeclared Peanuts

    Killer Brownie Distributing LLC is recalling Killer Brownie products due to undeclared peanuts. The mislabeled items were distributed to five states.

    Product
    NOT-A-NUTTER KB KILLER BROWNIE¿ 3x35 CT NET WT 36 LBS (16.33 kg) CONTAINS: Milk, Soy, Wheat UPC 10858061005314. Item #482-2016
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-2173-2017·2017-05-10

    Killer Brownie German Chocolate Brownies Recalled for Undeclared Peanuts

    Killer Brownie Distributing LLC is recalling German Chocolate Killer Brownies due to undeclared peanuts, a potential allergen hazard.

    Product
    GERMAN CHOCOLATE KB KILLER BROWNIE¿ 3x35 CT NET WT 36 LBS (16.33 kg) CONTAINS: Milk, Nuts: Pecans, Soy, Wheat UPC 10858061005321. Item #483-2016
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-2182-2017·2017-05-10

    Beyond Meat Recalls Feisty Crumbles for Undeclared Peanuts

    Beyond Meat is recalling specific lots of Beyond Beef Feisty Crumbles due to undeclared peanuts. The recall covers products distributed in California, Florida, Missouri, and Illinois.

    Product
    Beyond Beef Feisty Crumble Vegan Gluten-free Non-GMO Weight: 10 lbs. (2) 5 lb. bags UPC: 10852629004412 KEEP FROZEN 111 Main Street El Segundo, CA 90245 866-756-4112 [email protected] www.beyondmeat.com; Beyond Meat Beyond Beef Crumbles Feisty Net WT 11oz (312g) KEEP FROZEN
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2176-2017·2017-05-10

    Killer Brownie Peanut Butter Brownies Recalled for Undeclared Peanuts

    Killer Brownie Distributing LLC is recalling Peanut Butter KB Killer Brownies due to undeclared peanuts. The product was distributed to five states.

    Product
    PEANUT BUTTER KB KILLER BROWNIE¿ 3x35 CT NET WT 36 lbs (16.33 kg) CONTAINS: Milk, Nuts: Peanuts, Soy, Wheat UPC 10858061005048 . Item # 484-2016
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2183-2017·2017-05-10

    Urban Remedy Recalls Mislabeled Cold Pressed Apple Juice

    Urban Remedy is voluntarily recalling 656 bottles of Whole Foods Market Cold Pressed Juice, Apple, because the product was mislabeled and contains undeclared tree nuts.

    Product
    Whole Foods Market Cold Pressed Juice, Apple; 16 FL. Oz. (1 pt) 473 mL. Keep refrigerated - Enjoy within 5 days of opening. UPC 8 13377 02154 3
    Category
    Food
    Distribution
    3 states