The Recall Desk

Hazard

Mis Labeling recalls

9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,606
Critical
160
Severe
588
Most recent
2026-09-09

Of the 9,606 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.

1326–1350 of 9606

  • HighFDA (Devices)·Z-0052-2022·2021-10-13

    ZOLL SOLEX 7 Intravascular Catheter Kit Recalled for Potential Leakage

    ZOLL Circulation is recalling 98 units of SOLEX 7 intravascular heat exchange catheter kits due to potential leaks in the catheter or start-up kit tubing. A labeling update has been issued to address the safety concern.

    Product
    Zoll REF: 8700-0793-14 (SL-2593CO), SOLEX 7 Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens), Heparin COATED, Sterile EO, Rx Only, UDI: (01)00849111075541
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0038-2022·2021-10-13

    Cardiac Cooler-Heater Device Lacks Maintenance and Inspection Guidance

    CardioQuip is recalling its Modular Cooler-Heater device because labeling omits proper guidance for water-quality maintenance and device inspection, affecting users' ability to maintain the device correctly.

    Product
    CardioQuip, Modular Cooler-Heater 1000(m),Thermoelectric Cooling Lid, Model: MCH-11TEC,CE 2797, UDI: (01) 00860000846134
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0005-2022·2021-10-13

    Meclizine HCl Tablets 25 mg Recalled for Incorrect Instructions

    Rising Pharmaceuticals is recalling Meclizine HCl Tablets 25 mg (Lot # CB21024, expiring 2/2023) due to incorrect labeling instructions on the packaging.

    Product
    Meclizine HCl Tablets, 25 mg, packaged in 100-count HDPE bottle, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ 08816, Manufactured by: Aurex laboratories LLC, East Windsor, NJ 08520, NDC 16571-752-01
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0033-2022·2021-10-13

    Medical Device Calibrator Kit Recall for Incorrect Labeling

    FDA recalls Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit due to incorrectly labeled calibrator vials in Lot 00681Y600. The labeling error prevents the instrument from completing calibration successfully.

    Product
    Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit (ref 07P5605) - Product Usage: use in the calibration of the Alinity c CRP Vario assay, Cardiac CRP high sensitivity method [Cardiac CRP], on the Alinity c analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2543-2021·2021-10-06

    Carotid and Gelsoft vascular patches recalled for incorrect instructions

    Vascutek vascular patches were distributed with rest-of-world instructions instead of U.S. instructions. The 159 units distributed to Puerto Rico and Guam have incorrect Instructions for Use for U.S. use.

    Product
    The Instructions for Use (IFU) for: Carotid Patch and Gelsoft Patch vascular patches. FSN says Tapered Carotid Patch 920875t
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1026-2021·2021-10-06

    Grab & Go Bistro Pimento Cheese Sandwich Recalled for Undeclared Fish Allergen

    Modern Distributors, Inc. is recalling Grab & Go Bistro Pimento Cheese Sandwiches because they contain fish that is not declared on the label. The product was distributed through vending machines in Kentucky.

    Product
    Grab & Go Bistro Pimento Cheese Sandwich 5oz plastic container 1 sandwich per package
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1023-2021·2021-10-06

    Crunchy Cones Chocolate recalled for undeclared sulfites

    Borinquen Cones of Puerto Rico is recalling Crunchy Cones Chocolate (12-count, 40oz boxes, Lot 24521) because the product label does not declare the presence of sulfites.

    Product
    Crunchy Cones, Chocolate, 12, NET WT 40oz (113g)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2494-2021·2021-09-29

    Ad-Tech Medical Cable Recalled Due to Incorrect Product Labels

    Ad-Tech Lightweight CABRIO Cables with incorrect labels are being recalled. Mislabeling could cause product misidentification affecting proper use in clinical monitoring applications.

    Product
    Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1015-2021·2021-09-29

    Lemon Blueberry Scones Recalled for Undeclared Milk Allergen

    Baker's Corner Bakery is recalling Lemon Blueberry Scones because milk is not declared in the "Contains" statement, even though butter and buttermilk are listed in the ingredients. Consumers with milk allergies may be at risk.

    Product
    Lemon Blueberry Scones, packed in closed box, net wt. 12 oz. The label of affected product is read in parts: "*** Lemon Blueberry Scones*** Ingredients: Shepherds Grain Flour (wheat our, malted barley our, niacin, reduced iron, thiamine, mononitrate, ribo avin, folic acid), de
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1013-2021·2021-09-29

    Baker's Corner Bakery Chocolate Chip Cookies Recalled for Undeclared Soy

    Baker's Corner Bakery is recalling Chocolate Chip Cookies because soy-containing ingredients—soybean oil in the shortening and soy lecithin in the chocolate chips—are not declared on the label.

    Product
    Chocolate Chip Cookie, packed in closed bags, 12oz net wt. The label of affected label is read in parts: "***Chocolate Chip Cookie***Ingredients: Shepherds Grain Flour (wheat our, malted barley our, niacin, reduced iron, thiamine, mononitrate, ribo avin, folic acid), chocolate
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1010-2021·2021-09-29

    Baker's Corner Oatmeal Cranberry Cookies Recalled for Undeclared Soybean Oil

    Baker's Corner Bakery is recalling Oatmeal Cranberry Cookies because soybean oil is not declared on the label, despite being present in the shortening ingredient. Consumers with soy allergies may be at risk.

    Product
    Oatmeal Cranberry Cookie, packed in closed bags, 12oz net wt. The label of affected product is read in parts: "***Oatmeal Cranberry Cookie*** Ingredients: Oats, dried cranberries, Shepherds Grain Flour (wheat flour, malted barley flour, niacin, reduced iron, thiamine, mononitrat
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2495-2021·2021-09-29

    Ad-Tech TECH ATTACH Cable Recalled for Incorrect Label Information

    Ad-Tech Medical recalled its Lightweight TECH ATTACH Cable due to incorrect labels on affected units. The cables are designed to connect electrodes to third-party monitors and stimulators.

    Product
    Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2520-2021·2021-09-29

    Decompression Needle Recall Due to Incorrect Instructions for Use

    North American Rescue is recalling 51,424 units of 10 ga ARS Decompression Needles due to incorrect Instructions for Use. Affected parties should stop using and contact manufacturer.

    Product
    10 ga ARS Decompression Needle, Part Number ZZ-0298
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2496-2021·2021-09-29

    Ad-Tech TECH ATTACH Cable Recalled Due to Incorrect Labeling

    Ad-Tech Medical Instrument Corporation is recalling TECH ATTACH Cables due to incorrect labeling. The cables connect electrodes to third-party monitors and stimulators.

    Product
    Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·032-2021·2021-09-23

    Ready Pac Foods Recalls Salads with Undeclared Anchovy Allergen

    Ready Pac Foods is recalling ready-to-eat salads containing meat and poultry because they include salad dressing with an undeclared anchovy allergen.

    Product
    Ready Pac Foods, Inc. Recalls Ready to Eat Salad Products Containing Meat and Poultry Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0983-2021·2021-09-22

    Trader Joe's Raw California Walnut Baking Pieces Mispackaging Recall

    Trader Joe's Raw California Walnut Baking Pieces have been recalled due to mispackaging. Bags labeled as walnut pieces contain a mix of cashews, macadamia nuts, and walnuts.

    Product
    Trader Joe's Nuts Raw California Walnut Baking Pieces NET WT. 16 OZ (1 LB) 454g SKU# 51934-89685 UPC 0051 9342 Contains Walnuts Dist & Sold Exclusive By: Trader Joe's, Monrovia, CA 91016
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0984-2021·2021-09-22

    Albanese Mini Gummi Butterflies recalled for undeclared dietary supplement

    Albanese World's Best Mini Gummi Butterflies (7.5oz) contain comingled Olly Sleep dietary supplement that may cause drowsiness. Consumers should not eat the product.

    Product
    Albanese World's Best Mini Gummi Butterflies 7.5oz UPC 634418523525
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0981-2021·2021-09-22

    Roasted Red Pepper Flour Wraps Recall Due to Undeclared Wheat

    Tortilleria Sonora is recalling Roasted Red Pepper 12" Supreme Flour Wraps because the product contains undeclared wheat. The case label lists enriched flour but fails to disclose wheat presence, posing a risk to consumers with wheat allergies.

    Product
    Roasted Red Pepper 12" Supreme Flour Wraps, Tortilleria Sonora, Inc.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0956-2021·2021-09-15

    Fermentation Derived Pepsin recalled for undeclared egg allergen

    Ingredion is recalling Fermentation Derived Pepsin due to undeclared egg allergen. The affected product was distributed across multiple U.S. states.

    Product
    Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample bags packaged in 25 kg HDPE Drums
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2427-2021·2021-09-15

    Philips HEARTSTART Infant/Child Defibrillator Pads Recalled for Incorrect Labeling

    Philips infant/child defibrillator pads are recalled due to incorrect labeling that could delay therapy or result in lower energy delivery than indicated.

    Product
    Philips, HEARTSTART, INFANT/CHILD - SMART PADS CARTRIDGE, REF: M5072A, (0-8 YEARS)< 55 lbs / 25 kg, CE 0123, NON-STERILE, Rx only, UDI: (01) 00884838023758 for use with defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2426-2021·2021-09-15

    Medical diagnostic kit requires more frequent calibration than Instructions stated

    The Instructions for Use for Siemens' Atellica IM BR 27.29 Test Kit incorrectly specified a 10-day calibration interval instead of 3 days. The manufacturer has updated the instructions for all kit lots.

    Product
    Atellica IM BR 27.29 (BR) Assay 250 Test Kit (Reference)- in vitro diagnostic use in the quantitative serial determination of cancer antigen CA 27.29 in human serum and plasma (EDTA) using the Atellica IM Analyzer.- SMN: 11206236
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2425-2021·2021-09-15

    Medical Device Test Kit Requires More Frequent Calibration Than Labeled

    Siemens Atellica IM BR 27.29 test kit requires calibration every 3 days instead of the labeled 10-day interval. The product's calibration performance does not meet its Instructions for Use specifications.

    Product
    Atellica IM BR 27.29 (BR) Assay 250 Test Kit- in vitro diagnostic use in the quantitative serial determination of cancer antigen CA 27.29 in human serum and plasma (EDTA) using the Atellica IM Analyzer. SMN: 10995477
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-09102021·2021-09-10

    FSIS Recalls Meat Snack Breadsticks Due to Misbranding and Undeclared Sesame Ingredient

    FSIS issued a public health alert for ready-to-eat breadsticks and meat and cheese snack packs from Jag Specialty Foods that were misbranded because sesame was not declared on the label.

    Product
    FSIS Issues Public Health Alert For Meat Snack Products Containing FDA-Regulated Breadstick Products That Have Been Recalled Due To Misbranding And An Undeclared Ingredient
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2386-2021·2021-09-08

    Peripheral Atherectomy Devices Recalled Due to Crown Size Mislabeling

    Cardiovascular Systems Inc is recalling STEALTH 360 GEN2 peripheral atherectomy devices due to potential mislabeling of crown sizes. Some 1.50mm crowns may be labeled as 1.25mm and vice versa, potentially affecting device performance.

    Product
    STEALTH 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM, 1.25MM MICRO, 145 CM, REF PRD-SC30-MICRO
    Category
    Medical Device
    Distribution
    Distributed nationwide