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.

4126–4150 of 9607

  • ModerateFDA (Devices)·Z-0200-2018·2017-12-13

    Exactech Vantage Total Ankle Tibial Insert Recalled for Labeling Mismatch

    Exactech is recalling nine Vantage Total Ankle Tibial Inserts due to possible mismatches between inner and outer packaging labels.

    Product
    Vantage Total Ankle Tibial Insert, Fixed Bearing, 7 mm, Left, Size 3. Exactech Inc., Intended for patients with ankle joints damage by severe rheumatoid, post-traumatic, or degenerative arthritis. It is also indicated for revision of failed previous reconstructions where su
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0590-2018·2017-12-13

    C.R. Bard Recalls Arctic Sun ArcticGel Pads Due to Labeling Error

    C.R. Bard is recalling 128 units of Arctic Sun ArcticGel Pads - Medium because the product box displays an incorrect reference number.

    Product
    Arctic Sun ArcticGel Pads - Medium, Product Code 317-07
    Category
    Medical Device
    Distribution
    0 states
  • ModerateNHTSA·17V790000·2017-12-08

    Forest River Recalls 2018 Salem and Wildwood Trailers for Incorrect Tire Placards

    Forest River is recalling 2018 Salem and Wildwood recreational trailers because the Federal Placard incorrectly lists the tire size, which could lead to the installation of wrong-sized tires.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0396-2018·2017-12-06

    Pure Encapsulations Systemic Enzyme Complex Recalled for Undeclared Sulfites

    Pure Encapsulations is recalling Systemic Enzyme Complex dietary supplements because they contain undeclared sulfites. The products were distributed in five states.

    Product
    Pure Encapsulations Systemic Enzyme Complex DIETARY SUPPLEMENT 180 CAPSULES UPC: 7 66298 00862 2
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0174-2018·2017-12-06

    Siemens Dimension Vista Protein 1 Control Recalled for Inaccurate Ceruloplasmin Assignment

    Siemens Healthcare Diagnostics is recalling Dimension Vista Protein 1 Control lots due to inaccurate ceruloplasmin assignment, which may cause patient results to fall below the reference range.

    Product
    Dimension Vista Protein 1 Control, PROT 1 CON L, Siemens Material Number (SMN) 10445919, Product Code KC715; IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0175-2018·2017-12-06

    Siemens Dimension Vista Protein 1 Control M Recalled for Inaccurate Ceruloplasmin Results

    Siemens Healthcare Diagnostics is recalling Dimension Vista Protein 1 Control M units because they may produce inaccurate ceruloplasmin results below the reference range.

    Product
    Dimension Vista Protein 1 Control M, PROT 1 CON M, Siemens Material Number (SMN) 10445920, Product Code KC716; IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0392-2018·2017-12-06

    Dark Chocolate Cashew Recalled for Undeclared Milk Allergen

    Dutch Valley Food Distributors is recalling Dark Chocolate Cashew because the supplier failed to declare milk as an allergen, resulting in missing label information.

    Product
    Dark Chocolate Cashew, Net 11 oz., Contains Cashew and Soy, Distributed By: Dutch Valley Food Distributors, Inc., Myerstown, PA 17067; UPC: 77245 00601; Lot#, Best By dates: 20160404, 04/14/17;
    Category
    Food
    Distribution
    26 states
  • HighFDA (Food)·F-0391-2018·2017-12-06

    Dark Chocolate Almond Recalled for Undeclared Milk Allergen

    Dutch Valley Food Distributors is recalling Dark Chocolate Almond products because the supplier failed to declare milk as an allergen, resulting in missing label information.

    Product
    Dark Chocolate Almond, Net 11 oz., Contains Almond and Soy, Distributed By: Dutch Valley Food Distributors, Inc., Myerstown, PA 17067; UPC: 77245 00605; Lot#, Best By dates: 20160512, 05/12/17; 20160609, 06/9/17; 20160811, 08/11/17; 20160923, 09/23/17; 20161115, 11/15/17; 2017
    Category
    Food
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-0188-2018·2017-12-06

    Medtronic Recalls Everflex Self-Expanding Peripheral Stents Due to Labeling Error

    Medtronic is recalling 21 units of Everflex Self-Expanding Peripheral Stents because the stent length on the label may not match the actual stent length.

    Product
    Everflex Self-Expanding Peripheral Stent with Entrust Delivery System Intended to improve luminal diameter in the treatment of symptomatic de-novo or restenotic lesions up to 140 mm in length in the native Superficial Femoral Artery (SFA) and/or proximal popliteal arteries with
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0191-2018·2017-12-06

    Siemens N/T Protein Control SL Recalled for Inaccurate Ceruloplasmin Values

    CSL Behring GmbH is recalling Siemens N/T Protein Control SL products because they were incorrectly value-assigned, leading to biased ceruloplasmin test results.

    Product
    SIEMENS N/T Protein Control SL for use on the BN II, BN ProSpec Systems: N/T Protein Control SL/L: REF/Product Code OQIN19, SMN 10446079 (Low); N/T Protein Control SL/M, REF/Product Code OQIO19, SMN 10446085 (Mid); N/T Protein Control SL/H, REF/Product Code OQIP19, SMN 10446089
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0190-2018·2017-12-06

    Siemens N Protein Standard SL Recalled for Inaccurate Ceruloplasmin Calibration

    CSL Behring GmbH is recalling Siemens N Protein Standard SL and N/T Protein Controls SL due to incorrect value assignments that cause negative bias in Ceruloplasmin test results.

    Product
    SIEMENS N Protein Standard SL, for use on the BN II, BN ProSpec Systems, REF/Product Code OQIM 13, Siemens Material Number (SMN)10446073
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0397-2018·2017-12-06

    Pure Encapsulations AI Enzymes Recalled for Undeclared Sulfites

    Pure Encapsulations is recalling AI Enzymes dietary supplements because they contain undeclared sulfites. The products were distributed in five states.

    Product
    pure encapsulations AI Enzymes DIETARY SUPPLEMENT 120 CAPSULES UPC: 7 66298 00318 4 and 60 CAPSULES UPC: 7 66298 00317 7
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0408-2018·2017-12-06

    Reese Pharmaceutical Recalls Berry Flavor Immune Support Tablets for Labeling Error

    Reese Pharmaceutical is recalling Berry Flavor Immune Support Dietary Supplement Effervescent Tablets because the label fails to list sodium in the ingredient statement.

    Product
    Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. Product is sold under the following brand names: Discount Drug Mart UPC 0 93351 01230 3; Good Neighbor Pharmacy UPC 0 87701 41330 8; Hyvee UPC 0 75450 09537 1; Kinray Preferred Plus UPC 0 23513
    Category
    Food
    Distribution
    40 states
  • ModerateFDA (Devices)·Z-0183-2018·2017-12-06

    BD Insulin Syringes Recalled for Incorrect Needle Length Labeling

    Becton Dickinson is recalling specific lots of BD Insulin Syringes because some polybags were mislabeled with the wrong needle length and gauge.

    Product
    BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G, Catalog/REF 328466 BD Insulin Syringes are intended for the subcutaneous injection of insulin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0409-2018·2017-12-06

    Reese Pharmaceutical Recalls Orange Flavor Immune Support Effervescent Tablets

    Reese Pharmaceutical is recalling Orange Flavor Immune Support Effervescent Tablets because the label does not list sodium in the ingredient statement.

    Product
    Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10 Tablets/bottle. Product is sold under the following brand names: Best Choice UPC 0 70038 60863 9 & UPC 0 70038 60863 9; Discount Drug Mart UPC 0 93351 00909 9; Freds Mart UPC 0 84579 12451 0; Good Neighbor Ph
    Category
    Food
    Distribution
    40 states
  • CriticalUSDA FSIS·127-2017·2017-12-01

    Rafedain Shish Kabob Recalls Chicken Patties Due to Undeclared Allergens

    Rafedain Shish Kabob Restaurant is recalling chicken patty shish kabobs because they contain undeclared milk, wheat, and soy.

    Product
    Rafedain Shish Kabob Restaurant, Inc. Recalls Chicken Patty Shish Kabob Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0416-2018·2017-11-29

    Rich Products Recalls Mislabeled Macadamia Nut Cookie Dough

    Rich Products Corp is recalling Brewhouse Macadamia Nut Cookie Dough because it is mislabeled and actually contains peanut butter cookie dough.

    Product
    Brewhouse Macadamia Nut Cookie Dough Net Case Wt.: 26 LB 4 oz.. Frozen Net Unit Wt. 3 oz. Approximate Count:140 Product Code: 13804 UPC: 0 00 49800 13804 9
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0321-2018·2017-11-29

    GKI Foods Recalls Dark Chocolate Coffee Beans for Undeclared Milk

    GKI Foods is voluntarily recalling Dark Chocolate Coffee Beans because they may contain an undeclared milk allergen.

    Product
    Dark Chocolate Coffee Beans, 10 lbs., 15 lbs., 25 lbs., 12 pch Display, 8/8 oz., 12/10 oz., 12/8 oz.,
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-0385-2018·2017-11-29

    Woodstock Farms Dark Chocolate Cashews Recalled for Missing Milk Labeling

    United Natural Trading Inc. is recalling Market Basket Dark Chocolate Cashews because the label failed to list milk fat as an ingredient or include a 'contains milk' statement.

    Product
    Market Basket Dark Chocolate Cashews 8/12oz.
    Category
    Food
    Distribution
    0 states