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.

3476–3500 of 9607

  • ModerateFDA (Food)·F-1614-2018·2018-07-18

    Blue Bell Vanilla Ice Cream Cups Recalled for Missing Allergen Labeling

    Blue Bell Creameries is recalling 136 boxes of 3-ounce vanilla ice cream cups because they were distributed for retail sale without required nutrition and allergen labels.

    Product
    Blue Bell Ice Cream, Brand Homemade Vanilla Flavored, 3 FL OZ (88 mL), Cups, 24 per box, This Unit Not Labeled For Retail Sale
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2382-2018·2018-07-18

    Arrow International Recalls VPS Rhythm ECG Accessory Packs for Labeling Issues

    Arrow International Inc. is recalling 2,070 units of VPS Rhythm ECG Accessory Packs because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.

    Product
    VPS Rhythm ECG Accessory Pack with Johans Adapter, REF RHY-100-ECGJ Product Usage: To provide real time tip location information of a central venous catheter by utilization of ECG to observe P-wave changes as the tip approaches the right atrium of the heart via the Superior V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2425-2018·2018-07-18

    Dako PD-L1 IHC 22C3 pharmDx Recall for Storage Time Correction

    Dako North America Inc. is recalling 1,051 PD-L1 IHC 22C3 pharmDx kits to correct instructions for use regarding storage time for specific tissue sections.

    Product
    PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to determine PD-L1 levels for determination of patient treatment options.
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-2383-2018·2018-07-18

    Arrow International Recalls VPS Rhythm ECG Accessory Packs Due to Labeling Issues

    Arrow International is recalling 2,070 VPS Rhythm ECG Accessory Packs because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.

    Product
    VPS Rhythm ECG Accessory Pack, REF RHY-100-ECGO Product Usage: To provide real time tip location information of a central venous catheter by utilization of ECG to observe P-wave changes as the tip approaches the right atrium of the heart via the Superior Vena Cava (SVC). The
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0919-2018·2018-07-18

    Medi-Fare Recalls Potassium Chloride Syringes Due to Fill Volume Error

    Medi-Fare Drug and Home Health Center is recalling 1,116 syringes of Potassium Chloride For Injection Concentrate because they were filled with 19 mL instead of the labeled 20 mL.

    Product
    Potassium Chloride For Injection Concentrate syringe 40 mEq/20 mL (2 mEq/mL), Rx only, Medi-Fare Drug Pharmaceutical Compounding 300 West Pine St., Blacksburg, SC 29702 800-622-0007
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2385-2018·2018-07-18

    Arrow International Recalls Midline Catheter Kits Due to Labeling Issues

    Arrow International is recalling 2,070 Peripherally Inserted Midline Catheter Kits because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.

    Product
    Peripherally Inserted Midline Catheter Kit with Placement Wire, REF MK-02031-TW Product Usage: To provide real time tip location information of a central venous catheter by utilization of ECG to observe P-wave changes as the tip approaches the right atrium of the heart via th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2384-2018·2018-07-18

    Arrow International Recalls VPS TipTracker Stylet Accessory Due to Labeling Issues

    Arrow International Inc. is recalling 2,070 units of the VPS TipTracker Stylet Accessory because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.

    Product
    VPS TipTracker Stylet Accessory, REF RHY-177-TTSAP Product Usage: To provide real time tip location information of a central venous catheter by utilization of ECG to observe P-wave changes as the tip approaches the right atrium of the heart via the Superior Vena Cava (SVC). T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·18V468000·2018-07-13

    Forest River Recalls 2019 Palomino Campers Due to Incorrect Weight Label

    Forest River is recalling 2019 Palomino hardside truck campers because the Federal Placard lists an incorrect dry weight, which may result in the vehicle being overloaded.

    Product
    FOREST RIVER — FOREST RIVER PALOMINO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0911-2018·2018-07-11

    Fagron Recalls Neostigmine Methylsulfate Syringes Due to Labeling Error

    Fagron Compounding Services is recalling 390 prefilled syringes of Neostigmine Methylsulfate Injection Solution because some may be incorrectly labeled with the wrong strength.

    Product
    Neostigmine Methylsulfate Injection Solution, 3 mg per 3 mL, 1 mg per mL, 3 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0910-2018·2018-07-11

    Fagron Recalls Neostigmine Methylsulfate Syringes Due to Labeling Error

    Fagron Sterile Services is recalling 840 prefilled syringes of Neostigmine Methylsulfate Injection Solution because they may be incorrectly labeled with the wrong strength.

    Product
    Neostigmine Methylsulfate Injection Solution, 5 mg per 5 mL, 1 mg per mL, 5 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1606-2018·2018-07-11

    Icelandic Provisions Recalls Vanilla Skyr Cups Due to Coconut Mislabeling

    Icelandic Provisions Inc. is recalling Vanilla Skyr cups that may contain coconut skyr yogurt. The recall addresses a labeling error regarding the product flavor.

    Product
    Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC: 854074006068
    Category
    Food
    Distribution
    9 states
  • LowFDA (Devices)·Z-2332-2018·2018-07-11

    Ecolab Microtek Rolled Probe Cover Recalled for Incorrect Instructions

    Ecolab Inc. is recalling 65 cases of Microtek Rolled Probe Covers because they were shipped with incorrect instructions for use.

    Product
    ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905, packaged 1 probe cover/pouch, 25 pouches/carton, 2 cartons/shipping case, Sterile, RX. To be used as a physical barrier for protection against the effects of environmental exposure (e.g. body flui
    Category
    Medical Device
    Distribution
    6 states
  • LowFDA (Devices)·Z-2333-2018·2018-07-11

    Ecolab Microtek Rolled Probe Cover Recalled for Incorrect Instructions

    Ecolab Inc. is recalling 65 cases of Microtek Rolled Probe Covers because the products were shipped with incorrect instructions for use.

    Product
    ECOLAB MICROTEK Rolled Probe Cover, 2.6 cm x 20 cm (1 in x 8 in), Ref PC0906, packaged 1 probe cover/pouch, 25 pouches/carton, 2 cartons/shipping case, Sterile, RX. To be used as a physical barrier for protection against the effects of environmental exposure (e.g. body fluid
    Category
    Medical Device
    Distribution
    6 states
  • LowFDA (Drugs)·D-0892-2018·2018-07-11

    Qualgen Recalls Estradiol Pellets Due to Incorrect or Missing Lot and Expiration Dates

    Qualgen, LLC is recalling Estradiol 20mg Pellets because the vials have incorrect or missing lot and expiration dates.

    Product
    ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-020-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0893-2018·2018-07-11

    Qualgen Recalls Testosterone Pellets Due to Incorrect Lot and Expiration Dates

    Qualgen, LLC is recalling Testosterone 200 mg Pellets because the vials have incorrect or missing lot and expiration dates.

    Product
    TESTOSTERONE 200 mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-120-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2377-2018·2018-07-11

    Medtronic MiniMed Paradigm Veo Insulin Pump Recalled for Arabic Translation Error

    Medtronic is recalling 239,859 MiniMed Paradigm Veo insulin pumps due to an error in the Arabic language translation of the Predictive Alerts setting screen.

    Product
    Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Drugs)·D-0907-2018·2018-07-11

    Equate ClearLAX Recalled for Unfiled NDC Numbers on Labeling

    Lupin Somerset is recalling Equate ClearLAX laxative bottles due to unfiled NDC numbers on the labels. This is a Class III recall with no reported health risks.

    Product
    Equate ClearLAX, Polyethylene Glycol 3350 Powder for Solution, OS Osmotic Laxative, OTC, packaged in a) 119 g bottle (NDC 49035-312-07), b) 238 g bottle (NDC 49035-312-08), Distributed by: Wal-mart Stores, Inc., Bentonville, AR 72716
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·059-2018·2018-07-06

    Tillamook Country Smoker Recalls Teriyaki Beef Jerky Due to Misbranding

    Tillamook Country Smoker is recalling approximately 102 pounds of teriyaki beef jerky because the products may contain undeclared monosodium glutamate (MSG).

    Product
    Tillamook Country Smoker, LLC — Recall Notification Report 059-2018 (Beef Jerky Products)
    Category
    Food
    Distribution
    2 states
  • ModerateNHTSA·18V448000·2018-07-05

    Keystone Recalls 2018-2019 Dutchmen Aerolite Trailers for Incorrect Rim Label

    Keystone RV Company is recalling 2018-2019 Dutchmen Aerolite recreational trailers because the Federal Certification Label lists the wrong rim size, which could lead to unsafe rim replacements.

    Product
    DUTCHMEN — DUTCHMEN AEROLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1585-2018·2018-07-04

    New Seasons Market Recalls Meyer Lemon Chia Muffins for Undeclared Egg

    New Seasons Market LLC is recalling Meyer Lemon Chia Muffins because the packaging fails to declare egg as an ingredient.

    Product
    Meyer Lemon Chia Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10953 2
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2289-2018·2018-07-04

    Zimmer Biomet Recalls Vanguard Knee Bearings Due to Packaging Mix-up

    Zimmer Biomet is recalling 48 Vanguard Complete Knee System tibial bearings because two lots were commingled, creating a risk that 14mm bearings are packaged in 12mm boxes or vice versa.

    Product
    Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The product is intended for use in knee joint replacement arthroplasties.
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Food)·F-1586-2018·2018-07-04

    New Seasons Market Recalls Blueberry Buckwheat Muffins for Undeclared Egg

    New Seasons Market LLC is recalling Blueberry Buckwheat Muffins because the packaging fails to declare egg as an ingredient.

    Product
    Blueberry Buckwheat Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10952 5
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1587-2018·2018-07-04

    New Seasons Market Recalls Vegan Chocolate Almond Muffins for Allergen Labeling

    New Seasons Market LLC is recalling Vegan Chocolate Almond Muffins because the packaging fails to declare almonds as an ingredient.

    Product
    Vegan Chocolate Almond Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10955 6
    Category
    Food
    Distribution
    2 states