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.

4426–4450 of 9607

  • ModerateFDA (Food)·F-2380-2017·2017-07-19

    Source Naturals Hydrogen Boost Capsules Recalled for Undeclared Boron

    Source Naturals Hydrogen Boost Capsules are being recalled because they contain low levels of undeclared boron. The recall covers 55,354 units distributed nationwide.

    Product
    Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1855: 60 count Bottle - Product SN1856; 6 count Bottle - Product SN2314; 30 count + 30
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2469-2017·2017-07-19

    3CS Organics Recalls Topfer Lactana Bio Infant Formula for Labeling Issues

    3CS Organics LLC is recalling Topfer Lactana Bio infant and follow-up formula because the product is not FDA approved and lacks complete English labeling.

    Product
    Topfer Lactana Bio 1 Anfangsmilch, 600g (3/case), Topfer Lactana Bio 2, Bio Folgemilch, 600g (3bx/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2535-2017·2017-07-19

    Starbucks PB & J Fruit and Veggies Recalled for Missing Soy Labeling

    Taylor Farms Texas, Inc. is recalling Starbucks PB & J Fruit and Veggies because soy lecithin was not listed as an ingredient in the chocolate covered raisins.

    Product
    Starbucks PB & J Fruit and Veggies 7.4 oz. (210 g) UPC: 7 62111 23607 4
    Category
    Food
    Distribution
    0 states
  • LowNHTSA·17V445000·2017-07-14

    Forest River Recalls 2017 Rockwood Travel Trailers for VIN Label Error

    Forest River is recalling 2017 Rockwood travel trailers because an incorrect check digit on the VIN label may hinder vehicle registration and safety recall tracking.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2412-2017·2017-07-12

    Albertsons Recalls Carrot Cake Slices Due to Missing Walnut Allergen Labeling

    Albertsons is recalling 191,885 carrot cake slices sold in California because the packaging failed to list walnuts as an ingredient or allergen.

    Product
    Carrot Cake Slice: Net Wt. 0 LB 7 OZ (198 g). Cake is assembled, iced, sliced and packaged at store level. Sliced wrapped individually in clear plastic clamshell and sold in bakery department. UPC Code: 0222132-000000 Sold under Albertsons Companies retail banners of Von
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2428-2017·2017-07-12

    Sea Watch Beer Battered Clam Strips Recalled for Undeclared Milk Allergen

    Sea Watch International is recalling Beer Battered Clam Strips because the bread coating may contain undeclared milk, which is not listed on the label.

    Product
    Sea Watch Brand Beer Battered Clam Strips Pack Size: 24/4 oz. bags/case
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2433-2017·2017-07-12

    Don's Salads Recalls Egg Salad Due to Undeclared Milk

    Don's Salads is recalling egg salad products because an ingredient used in their manufacture contains undeclared milk.

    Product
    Don's Salads; Egg Salad; Net Wt. 5 lbs., MFGD by Aldon Food Corp, Schwenksville, PA 19473; Sell by dates: 6/7, 6/9, 6/13, 6/15; UPC: 740247005061; AND; Block & Barrel Classic Egg Salad; Net Wt. 5 lbs; Distributed by Sysco Corporation, Houston, TX 77077; Sell By Dates: 6/7,
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-2416-2017·2017-07-12

    Greek Pasta Salad Recalled for Undeclared Milk Allergen

    A.S.K. Foods is recalling Taste of Inspirations Greek Pasta Salad because some packages have incorrect labels that do not list milk as an ingredient.

    Product
    Taste of Inspirations; Greek Pasta Salad, Net Wt. 10 oz.; Distributed By: DZA Brands, LLC, Salisbury, NC 28147/Scarborough, ME 04074;
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2455-2017·2017-07-12

    Meijer Cashews Recalled for Missing Coconut Allergen Labeling

    Meijer Distribution is recalling Meijer Cashews Toasted Coconut because the label lists a 'Contains' statement but omits coconut, a major allergen.

    Product
    MEIJER CASHEWS TOASTED COCONUT 8.25 OZ plastic pouch
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-2418-2017·2017-07-12

    Schnucks Bakery Cinnamon Pudding Cake Recalled for Undeclared Walnuts

    Schnucks Markets is recalling Cinnamon Pudding Cakes because the labels fail to declare the presence of walnuts, a major food allergen.

    Product
    1) Schnucks Bakery, Cinnamon Pudding Cake Slice, NET WT 6.0 oz (170 g); 2) Schnucks Bakery, Half Cinnamon Pudding Cake, NET WT 1.06 lb (482 g);
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2429-2017·2017-07-12

    Sailors Choice Breaded Clam Strips Recalled for Undeclared Milk

    Sea Watch International is recalling Sailors Choice Breaded Clam Strips because the bread coating may contain undeclared milk, a major allergen not listed on the label.

    Product
    Sailors Choice Brand Breaded Clam Strips Pack Size: 24/4 oz. bags/case
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-2448-2017·2017-07-12

    Sabor Mexicano Corn Chips Recalled for Sodium Labeling Error

    Sabor Mexicano is recalling Homemade Corn Chips because the label listed 15 mg of sodium instead of the correct 250 mg.

    Product
    Sabor Mexicano Homemade Corn Chips: Packaged in 12 oz. (9 units per case), UPC 8-53094-00417-7, and Fun size 5 oz. ( 12 units per case), UPC 8-53094-00418-4.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-2423-2017·2017-07-12

    Nutri-Dyn Calcium D-Glucarate Plus Recalled Due to Mislabeling

    Nutri-Dyn Midwest, Inc. is recalling 856 bottles of Calcium D-Glucarate Plus because they were mistakenly labeled as St. John's Wort during production.

    Product
    Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Devices)·Z-2687-2017·2017-07-12

    Mallinckrodt Recalls ArterX Surgical Sealant Due to Improper Labeling

    Mallinckrodt is recalling ArterX Surgical Sealant because improper labeling led to improper storage. The affected units were distributed to the UK.

    Product
    Tenaxis Medical ArterX(TM) Surgical Sealant, (a) 4mL, REF 9002, and (b) 5mL REF 9006, STERILE R, Store at 2oC - 8oC Adjunct to sutures in vascular surgery.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-2422-2017·2017-07-12

    Bacalafoods Recalls Finola Style Octopus in Oil Due to Mislabeling

    Bacalafoods Corp is recalling Finola Style Octopus in Oil because the product contains squid but is labeled as octopus.

    Product
    Finola, Style Octopus in Oil, Product of Spain, Wild Caught, Net Weight 4.1/10oz (115g), Empacado para:/Packaged for: Bacalafoods Corp., San Juan, PR 00936-8060
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2673-2017·2017-07-12

    Boston Scientific Retrieval Balloon Catheter Recalled for Labeling Error

    Boston Scientific is recalling 39 units of the Extractor Pro RX-S Retrieval Balloon Catheter because the label incorrectly identifies the injection location.

    Product
    Boston Scientific Extractor Pro RX-S Retrieval Balloon Catheter 9-12mm Above UPN: M00547300
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2674-2017·2017-07-12

    Boston Scientific Retrieval Balloon Catheter Recalled for Incorrect Injection Labeling

    Boston Scientific is recalling 32 units of Extractor Pro RX-S Retrieval Balloon Catheters because the labels incorrectly identify the injection location relative to the balloon.

    Product
    Boston Scientific Extractor Pro RX-S Retrieval Balloon Catheter 12-15mm Below UPN: M00547340
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2662-2017·2017-07-12

    Exactech Recalls Logic Fit Tibial Tamp Heads for Labeling Clarification

    Exactech, Inc. is recalling 573 Logic Fit Tibial Tamp Heads to update surgical labeling. The update clarifies proper removal techniques to prevent instrument breakage.

    Product
    Logic Fit Tibial Tamp Head
    Category
    Medical Device
    Distribution
    32 states
  • ModerateFDA (Food)·F-2421-2017·2017-07-12

    Bacalafoods Recalls Finola Style Octopus in Garlic Due to Mislabeling

    Bacalafoods Corp is recalling Finola Style Octopus in Garlic because the product contains squid instead of octopus. The recall covers 340 boxes distributed in Puerto Rico.

    Product
    Finola, Style Octopus in Garlic, Product of Spain, Wild Caught, Net Weight 4.1/10oz (115g), Empacado para:/Packaged for: Bacalafoods Corp., San Juan, PR 00936-8060
    Category
    Food
    Distribution
    1 state
  • LowFDA (Drugs)·D-0935-2017·2017-07-12

    PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling two Bupivacaine HCl ON-Q pumps due to incorrect or missing lot and expiration date labeling.

    Product
    Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 270 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-044-57
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0933-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Lot and Expiration Dates

    PharMEDium Services, LLC is recalling 10 Ropivacaine HCl 0.2% ON-Q pumps nationwide due to incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 750 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 600 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-279-33
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0936-2017·2017-07-12

    PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling seven Bupivacaine HCl ON-Q pumps because of incorrect or missing lot and expiration dates.

    Product
    Bupivacaine HCl 0.25% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-023-09
    Category
    Drug
    Distribution
    Distributed nationwide