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.

8326–8350 of 9611

  • HighFDA (Food)·F-0170-2014·2013-11-20

    Oh Bok Bakery Recalls Sweet Bread for Undeclared Wheat Flour

    Cho & So, Inc. DBA Oh Bok Bakery is recalling ASSI brand Sweet Bread (Bam Bbang) because wheat flour was not declared on the label.

    Product
    Sweet Bread known as Bam Bbang (Chestnut Bread) packed on styrofoam tray with plastic over wrap ASSI brand Korean Cake 20646D Net Wt.: 8 oz. Distributed by Rhee Bros., Inc. 7461 Coca Cola Dr Hanover, MD 21076 Expiration date 1/29/14 With Korean language labeling
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0275-2014·2013-11-20

    DeRoyal Surgical Eye Spears Recalled for Incorrect X-Ray Detectability Labeling

    DeRoyal Industries is recalling one lot of Surgical Eye Spears because they were labeled as x-ray detectable but contained non-detectable product.

    Product
    DeRoyal (R) Surgical Eye Spears, REF 30-049, Sterile EO, Manufacturer: DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849, MADE IN GUATEMALA cleaning of fluids from surgical site in or near the eye
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0272-2014·2013-11-20

    Biotene Moisturizing Mouth Spray Recalled for Incorrect Ingredient Labeling

    GlaxoSmithKline is recalling Biotene Moisturizing Mouth Spray because the label lists sorbitol, but the product does not contain it.

    Product
    Biotene Moisturizing Mouth Spray, with xylitol, For dry mouth symptom relief, 44.3ml/1.5 FL. OZ., Sugar Free Sweetened with xylitol and sorbitol, GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108. Biotene Mouth Spray is used for the treatment of dry mouth
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0276-2014·2013-11-20

    OrthoPediatrics Recalls 3.5mm Locking Screws Due to Packaging Labeling Error

    OrthoPediatrics Corp is recalling 3.5mm locking screws because the packaging description incorrectly identified them as 7.0mm screws, despite the correct part number.

    Product
    3.5MM LOCKING SCREW, T15 HEXALOBE, SELF TAPPING, 34MM The OrthoPediatrics Proximal Femur Plating System combines implants and instruments in one convenient system. This system offers the advantages of the osteotomy blade plates and cannulated instrumentation. Osteotomy plates
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0200-2014·2013-11-20

    Anspach Effort Recalls Pneumatic Systems Operating Manual and Product Catalog

    Anspach Effort, Inc. is correcting labeling on its Pneumatic Systems Operating Manual and Product Catalog because a claim regarding the device's capability to dissect biometals, bioplastics, and cement was found to be inaccurate.

    Product
    Product Catalog (part number 20-0020) utilized with the Electric and Pneumatic Motor Systems including: MicroMax Motor Systems, XMax Motor Systems, EMax2 Motor Systems, and Emax2Plus Motor Systems, all models and serial numbers. Product Usage: Indication for use is cutting an
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0199-2014·2013-11-20

    Anspach Effort Recalls Cutting Bur Chart Due to Labeling Error

    Anspach Effort, Inc. is correcting labeling on its Cutting Bur Chart and related manuals because a claim about cutting biometals was not part of the device's intended use.

    Product
    Cutting Bur Chart (part number 20-0019) utilized with the Electric and Pneumatic Motor Systems including: MicroMax Motor Systems, XMax Motor Systems, EMax2 Motor Systems, and Emax2Plus Motor Systems, all models and serial numbers. Product Usage: Indication for use is cutting
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0173-2014·2013-11-20

    Torn Ranch Fruit Truffles Recalled for Undeclared Yellow Dyes

    Torn Ranch Inc. is recalling specific fruit truffle flavors because Yellow #5 and #6 dyes were not declared on the label.

    Product
    Fruit Truffles - Cherry, Coconut, Key Lime, Lemon, Mango, Pear, Pineapple and Tangelo flavors. (6 piece count/4.5 oz) Pear, Lemon, Key Lime, Coconut flavors contain FD&C Y5 and/or Y6; (9 piece count/7 oz) Pear, Cherry, Tangelo, Coconut,
    Category
    Food
    Distribution
    10 states
  • LowFDA (Devices)·Z-0198-2014·2013-11-20

    Anspach Effort Pneumatic Systems Operating Manual Labeling Correction

    Anspach Effort is correcting labeling on Pneumatic Systems Operating Manuals to remove unverified claims about cutting biometals, bioplastics, and cement.

    Product
    Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the Pneumatic Motor Systems including: BlackMax Motor Systems, MicroMax Systems and XMax Motor Systems all models and serial numbers. Product Usage: Indication for use is cutting and shaping bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0121-2014·2013-11-13

    KCB Pista Khatie Cookies Recalled for Undeclared Egg Allergen

    Kashmir Crown Baking LLC is recalling Pista Khatie cookies because testing found undeclared egg allergen, despite the label stating the product contains no eggs.

    Product
    KCB Pista Khatie KCB Bakery Products Corp. 56-28 56th Street, Maspeth, NY 11378 Tel: (718) 786-9463 Fax (718) 361-0171 www.kbcusa.com a) Net Wt. 30 OZ (850 G) b) Net Wt. 13 OZ (369 G) Packaged in a plastic clam shell container with stick-on labels.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0122-2014·2013-11-13

    Safeway Recalls Angel Food Cake Due to Missing Milk and Soy Labels

    Safeway is recalling 70,162 units of Angel Food Cake because the labels omitted milk and soy ingredients, posing a risk to consumers with allergies.

    Product
    Angel Food Cake; labeled for retail sale in the following stores: Safeway, Carrs, Dominicks, Genuardis, Pak N Save, Pavilions, Randalls, Tom Thumb and Vons. Angel Food Cake 0 lb. 12 oz. (340 g) Black or White Base with Clear Lid
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-0115-2014·2013-11-13

    Yoders Country Market Recalls Honey Roasted Peanuts for Undeclared Allergens

    Yoders Country Market is recalling 24 units of Honey Roasted Peanuts in custom gift boxes because the product contains undeclared milk and wheat.

    Product
    Custom made gift boxes containing: HONEY ROASTED PEANUTS, Net Wt. 11 oz. (311G), Dist.By: Dutch Valley Food Distributors, Inc. Myerstown, PA 10787, UPC 8 77245 00143 3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0123-2014·2013-11-13

    Safeway Recalls Holiday Angel Food Cakes Due to Missing Allergen Labels

    Safeway is recalling Holiday Decorated Angel Food Cakes because the labels failed to list milk and soy as ingredients.

    Product
    Holiday Decorated Angel Food Cake; labeled for retail sale in the following stores: Safeway, Carrs, Dominicks, Genuardis, Pak N Save, Pavilions, Randalls, Tom Thumb and Vons. Holiday Decorated Angel Food Cake  1 lb. 14 oz. (850 g); Black or White Base with Clear Lid; fros
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-0126-2014·2013-11-13

    Safeway Angel Food Cake Recalled for Missing Soy Flour Labeling

    Safeway is recalling Angel Food Cake Fruit Topped because the ingredient label omitted soy flour, a major allergen.

    Product
    Angel Food Cake Fruit Topped; labeled for retail sale in the following stores: Safeway, Carrs, Dominicks, Genuardis, Pak N Save, Pavilions, Randalls, Tom Thumb and Vons. Angel Food Cake Fruit Topped  3 lb. 12 oz. (1701 g); Angel Food Cake Fruit Topped  Black or White Bas
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-0125-2014·2013-11-13

    Safeway Recalls Angel Food Cake Loaves Due to Allergen Labeling Errors

    Safeway is recalling Angel Food Cake Loaves because the labels failed to list milk and soy as ingredients.

    Product
    Cake Angel Food Loaf: 1) Cake Angel Food Loaf; labeled for retail sale in the following stores: Safeway, Carrs, Dominicks, Genuardis, Pak N Save, Pavilions, Randalls, Tom Thumb and Vons. Cake Angel Food Loaf 0 lb. 4 oz. (113 g) Cake Angel Food Loaf Individual loaf sold in p
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-0124-2014·2013-11-13

    Safeway Recalls Angel Food Cups Due to Missing Milk and Soy Allergen Labels

    Safeway is recalling 448 packages of Angel Food Cups because the labels failed to list milk and soy as ingredients.

    Product
    Angel Food Cups 4 Count; labeled for retail sale in the following stores: Safeway, Carrs, Dominicks, Genuardis, Pak N Save, Pavilions, Randalls, Tom Thumb and Vons. Angel Food Cups 4 Count  0 lb. 3 oz. (85g); Individual cake cups sold in package of 4 items.
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-0165-2014·2013-11-13

    Insulet Recalls OmniPod Insulin Starter Kits Due to Mislabeling

    Insulet Corporation is recalling 1,719 OmniPod Insulin Management System Starter Kits because the included alcohol prep pads are not properly labeled.

    Product
    OmniPod Insulin Management System Starter Kit; Model Reference Number: SKT-UST400 (Starter Kit) Product Usage: The Starter Kit (SKT-UST400) is provided to users as an introduction to the OmniPod Insulin Management System prior to initiating care. It includes the Personal Diab
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0145-2014·2013-11-13

    Richard Wolf Recalls S(a)line Resectoscope Vaporization Electrodes Due to Packaging Error

    Richard Wolf Medical Instruments Corp. is recalling S(a)line resectoscope vaporization electrodes because a different model was found packaged in the wrong pouch.

    Product
    Individual units labeled in part: REF: 4630022; for S(a)line resectoscopes; Vaporization electrode, sterite; 4mm telescope 30 25 / 12: only for continuous irrigation sheath 24,5 Fr.; LOT 426111; 2011/06; 2016/06; STERILE; RICHARD WOLF; Cartons of 3 units labeled in part: REF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0154-2014·2013-11-13

    Medtronic Resolute Integrity Coronary Stent Recall for Incorrect Compliance Chart Labeling

    Medtronic is recalling 201 units of Resolute Integrity Zotarolimus-eluting Coronary Stents because the compliance chart may incorrectly reference a 2.25 mm diameter instead of the correct 3.0 mm.

    Product
    Resolute Integrity Zotarolimus-eluting Coronary Stent: Stent ID 3.0 mm; Stent length 34 mm; Rx, Sterile. Mfg in Medtronic Ireland, Galaway, Ireland. Distributed by: Medtronic Inc. Minneapolis, MN. Indicated for improving coronary luminal diameters in patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0131-2014·2013-11-13

    Smith & Nephew Recalls Swapped Genesis II Tibial Base Implants

    Smith & Nephew is recalling four units of Genesis II tibial base implants due to packaging errors where size 5 left and size 6 right components were swapped.

    Product
    GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 6, RIGHT, QTY: (1), REF 71420188. Product Usage: orthopaedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0166-2014·2013-11-13

    Insulet Recalls OmniPod Demonstration Kits Due to Mislabeling

    Insulet Corporation is recalling 5,050 OmniPod Insulin Management Product Demonstration Kits because the included alcohol prep pads are not properly labeled.

    Product
    OmniPod Insulin Management Product Demonstration Kit; Model Reference Number: (PDK-ZXP490) Product Usage: The Demonstration Kit (PDK-ZXP490) is an alternate kit provided to potential patients by healthcare professionals for patients to experience what wearing a Pod may feel l
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0130-2014·2013-11-13

    Smith & Nephew Recalls Mispackaged Genesis II Tibial Base Components

    Smith & Nephew is recalling four units of Genesis II tibial base components due to size and side mislabeling.

    Product
    GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 5, LEFT, QTY: (1), REF 71420168. Product Usage: orthopaedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0082-2014·2013-11-06

    Amport Foods Chocolate Raisins Recalled for Peanut Mislabeling

    American Importing Co, Inc. is recalling Amport Foods Chocolate Raisins because a package of Milk Chocolate Peanuts was erroneously labeled as Milk Chocolate Raisins.

    Product
    Amport Foods Chocolate Raisins. Net Wt. 12 oz (340g). UPC 71725-71190. Allergy Information: This product is produced on equipment shared with peanuts and tree nut products.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0105-2014·2013-11-06

    Siemens RAPIDLab Blood Gas Analyzer Recall for Patient ID Error Risk

    Siemens is recalling RAPIDLab 1200 Series blood gas analyzers because users may enter the wrong patient ID, leading to sample misidentification.

    Product
    Siemens RAPIDLab¿ 1240 system blood gas analyzer Product Usage: RAPIDLab 1200 Systems: The Rapidlab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The systems can determine the following pa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0102-2014·2013-11-06

    Siemens RAPIDPoint 400 Blood Gas Analyzer Recalled for Sample Misidentification Risk

    Siemens Healthcare Diagnostics Inc. is recalling RAPIDPoint 400 series blood gas analyzers because users may enter incorrect patient IDs, leading to sample misidentification.

    Product
    Siemens RAPIDPoint¿ 400 system blood gas analyzer Product Usage: These systems are intended for near-patient and laboratory testing of blood gases, electrolytes, metabolites, total hemoglobin, and hemoglobin derivatives in arterial, venous, and capillary whole blood samples.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0087-2014·2013-11-06

    Pringles Salt and Vinegar Chips Recalled for Undeclared Milk Allergen

    Kellogg Canada is recalling Pringles Salt and Vinegar Potato Chips because the packaging failed to declare milk as an ingredient, violating Canadian labeling regulations.

    Product
    Pringles(R) SALT & VINEGAR Potato Chips, 168 g (UPC 064100852464) and 181 g (UPC 037000230090), Pringles Manufacturing Company, 1306 Highway 70 Bypass, Jackson, TN, USA 38301-5072
    Category
    Food
    Distribution
    0 states