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.

6676–6700 of 9611

  • LowFDA (Devices)·Z-1077-2015·2015-02-18

    Stryker Flyte Toga Recall Due to Incorrect Expiration Date Labeling

    Stryker is recalling Flyte Togas with an incorrect expiration date. The label reads 2412-12-01 instead of 2014-12-01.

    Product
    Flyte Togas are components of the Stryker Flyte System and are intended to be worn over any Stryker Flyte Helmet. This toga provides Level 1 and 4 protection according to the Association for the Advancement of Medical Instrumentation (AAMI) Liquid Barrier Performance and Classif
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1076-2015·2015-02-18

    MAST Biosurgery Recalls SurgiWrap Film Due to Expiration Date Mismatch

    MAST Biosurgery is recalling 49 units of SurgiWrap Bioresorbable Adhesion Barrier Film because the expiration date on the barcode did not match the printed date.

    Product
    The SurgiWrap Bioresorbable Adhesion Barrier Film. SurgiWrap 100x130x0.05mm (01) 18964050255027 (17) 170731(10)52804 LOT 52804 2017-08 REF25502-01 Product is wrapped in a foil pouch that is then sealed into an additional envelope.
    Category
    Medical Device
    Distribution
    0 states
  • HighUSDA FSIS·032-2015·2015-02-17

    Michigan Brand Recalls Pork Sausage for Undeclared Soy Allergen

    Michigan Brand Inc. is recalling pork sausage products because they contain undeclared hydrolyzed soy protein, a known allergen.

    Product
    Michigan Brand Inc. — Michigan Brand, Inc. Recalls Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0959-2015·2015-02-11

    Reily Foods Recalls Wick Fowler's Chili Kits for Undeclared Allergens

    Reily Foods is recalling Wick Fowler's Texas Style False Alarm Mild Chili Kits because they contain peanut and almond allergens that are not declared on the ingredient statements.

    Product
    WICK FOWLER'S TEXAS STYLE FALSE ALARM Mild Chili Kit, NET WT. 3.03 oz. (86g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-71092-00111-4
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1017-2015·2015-02-11

    FDA Recalls Covidien Trellis-6 Peripheral Infusion Systems Due to Labeling Error

    The FDA is recalling 216 units of the Covidien Trellis-6 Peripheral Infusion System because a manufacturing error caused the balloon inflation ports to be incorrectly labeled.

    Product
    Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Sterile EO. Product Usage: Intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0956-2015·2015-02-11

    Reily Foods Recalls Chili Kits With Undeclared Peanut and Almond Allergens

    Reily Foods is recalling Carroll Shelby's Original Texas Brand Chili Kits because they contain peanut and almond allergens not listed on the ingredient label.

    Product
    CARROLL SHELBY'S ORIGINAL TEXAS BRAND CHILI KIT, NET WT. 4 oz. (113 g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-72396-10000-8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0957-2015·2015-02-11

    Reily Foods Recalls White Chicken Chili Kits Due to Undeclared Allergens

    Reily Foods is recalling Carroll Shelby's Original Texas Brand White Chicken Chili Kits because they contain peanut and almond allergens not listed on the ingredient label.

    Product
    CARROLL SHELBY'S ORIGINAL TEXAS BRAND WHITE CHICKEN CHILI KIT, 3 oz. (85 g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-72396-10019-0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0958-2015·2015-02-11

    Reily Foods Recalls Chili Kits for Undeclared Peanut and Almond Allergens

    Reily Foods is recalling Wick Fowler's Famous Texas Style 2-Alarm Chili Kits because they contain peanut and almond allergens that are not declared on the ingredient statements.

    Product
    WICK FOWLER'S FAMOUS TEXAS STYLE 2-ALARM Chili Kit, NET WT. 3.6525 oz. (102g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-71092-00069-8
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1057-2015·2015-02-11

    Medtronic Recalls KYPHON EXPRESS Osteo Introducer System Due to Labeling Error

    Medtronic is recalling 239 units of the KYPHON EXPRESS Osteo Introducer System because the packaging may contain the wrong instrument tips.

    Product
    KYPHON EXPRESS, Osteo Introducer System, Diamond and Bevel, Size 2, REF T34A, QTY: 1EA, Rx only, STERILE R. For use with spinal fixation devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1037-2015·2015-02-11

    FDA Recalls 16cm Minimally Invasive Attachment Due to Incorrect Color Bands

    The Anspach Effort, Inc. is recalling 8 units of the MIA16-G1 Minimally Invasive Attachment because customer complaints indicated the color bands were not correct.

    Product
    16cm Minimally Invasive Attachment. For use with Motor Systems for cutting and shaping bones, including the spine and cranium. Model MIA16-G1
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1047-2015·2015-02-11

    Fresenius Crit Line in a Clip Monitor Recalled for Display Misinterpretation

    Fresenius Medical Care is recalling 35 Crit Line in a Clip monitors due to a potential for misinterpretation of the Blood Volume slope graphic display.

    Product
    Fresenius Crit Line in a Clip (CLiC) with SW version 2.51 Model Number: CL10041001. A continuous real-time monitor for non-invasive hematocrit, oxygen saturation and percent change in blood volume calculation during hemodialysis treatment.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1048-2015·2015-02-11

    Intuitive Surgical Recalls da Vinci Si Wall Charts for Sterilization Inconsistency

    Intuitive Surgical is recalling 1,034 da Vinci Si Wall Charts because they contained incorrect sterilization dry time information inconsistent with the User Manual.

    Product
    da Vinci Si Surgical System, IS3000; - Wall chart for EndoWrist Stapler 45 System. Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1033-2015·2015-02-11

    Express Diagnostics Recalls DrugCheck Ketamine Dip Tests for False Positives

    Express Diagnostics is recalling DrugCheck Ketamine Dip Tests because they may produce false positive results, leading to incorrect screening outcomes.

    Product
    DrugCheck Ketamine Dip Test 31317-3P PRO-EU-SWE, 31226-3-CA-GML, 30842 TR, 30108C, 30108C CAN, 30108C EU, and 30108C INT. This assay provides only a preliminary analytical test result.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1018-2015·2015-02-11

    FDA Recalls Covidien Trellis-8 Peripheral Infusion Systems Due to Labeling Error

    FDA is recalling 1,032 units of the Covidien Trellis-8 Peripheral Infusion System because a manufacturing error caused the proximal and distal balloon inflation ports to be incorrectly labeled.

    Product
    Covidien Trellis-8 Peripheral Infusion System. Models CVT808015, CVT808025, CVT812015, and CVT812025. The following models are not offered for sale in the US: EVT808015, EVT808025, EVT812015, and EVT812025 Sterile EO. Product Usage: Intended for controlled and selective in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0937-2015·2015-02-04

    Market Pantry Dark Chocolate Covered Almonds Recalled for Undeclared Peanuts

    Zachary Confections is recalling Market Pantry Dark Chocolate Covered Almonds because the product contains peanuts that are not declared on the label.

    Product
    Market Pantry Brand Dark Chocolate Covered Almonds 9 oz., UPC 085239555644
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-1009-2015·2015-02-04

    Synthes Mandible External Fixator Recalled for Incorrect MR Safe Labeling

    Synthes, Inc. is recalling Mandible External Fixators because updated testing protocols mean the devices can no longer be designated MR Safe, despite previous labeling.

    Product
    The Synthes Mandible External Fixator; all lots of part nos.: 04.305.003 04.305.004 04.305.005 04.305.010 04.305.011 04.305.012 03.305.006 04.305.100 04.305.101 04.305.102 04.305.103 04.305.128 04.305.130 04.305.134 04.305.138 04.305.140 04.305.142 03.305.105
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1012-2015·2015-02-04

    Aesculap Miethke Shunt System Accessories Recalled for Incorrect MR Safety Labeling

    Aesculap, Inc. is recalling Miethke Shunt System accessories because the shelf box labels incorrectly display an MR conditional symbol. The product is actually MR unsafe, and the correct information is only provided in the Instructions for Use.

    Product
    Miethke Shunt System accessories Product Usage: - The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·028-2015·2015-02-04

    Krehbiels Specialty Meats Recalls Pork Bratwurst Due to Misbranding

    Krehbiels Specialty Meats is recalling approximately 29 pounds of pork bratwurst because the label failed to list all ingredients due to a printing error.

    Product
    Krehbiels Specialty Meats Inc — Recall Notification Report 028-2015 (Bratwurst)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1028-2015·2015-02-04

    Smiths Medical Recalls Arterial Blood Sampling Kits Due to Labeling Error

    Smiths Medical ASD, Inc. is recalling 900 units of Portex Anaerobic Pulsator Arterial Blood Sampling Kits because the inner unit label displays an expiration date one year later than the actual date.

    Product
    Portex Anaerobic Pulsator Arterial Blood Sampling Kit, with Liquid Sodium Heparin for Gases and Electrolytes. Reorder Number: G1392 Product Usage: The Arterial Blood Sampling Kit is intended for sampling arterial blood for the measurement of blood gasses, Cooximetry, ele
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0796-2015·2015-01-28

    Giant Eagle Recalls Jumbo Lump Crab Cakes Due to Undeclared Milk

    Giant Eagle is recalling Jumbo Lump Crab Cakes in Pennsylvania and Ohio because the ingredient statement failed to declare milk.

    Product
    Jumbo Lump Crab Cakes packed from bulk into clam shell containers with Giant Eagle scale label 100% Jumbo Lump Crab Cake Sell by Date: any date Net Wt. any weight Giant Eagle Market District Distributed by Giant Eagle, Pittsburg, PA 15328
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0997-2015·2015-01-28

    Philips IntelliVue TcG10 Monitor Recalled for Missing Contraindication Warning

    Philips is recalling 86 IntelliVue TcG10 monitors because the instructions for use are missing a warning against using the device on patients under gas anesthesia.

    Product
    Philips IntelliVue TcG10; Monitor, carbon-dioxide, cutaneous. The IntelliVue TcG10 is a device for the measurement of the transcutaneous O2 and CO2 partial pressure in neonates, pediatrics and adults.
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Food)·F-0797-2015·2015-01-28

    Baroody Pickled Labneh Recalled for Undeclared Sorbic Acid and Sulfites

    Baroody Imports Inc. is recalling Baroody Pickled Labneh with Pepper because the product contains undeclared sorbic acid and sulfites.

    Product
    Baroody Pickled Labneh with Pepper, Net Wt. 20 oz., (1 lb. 4 oz.), 575-g, in sealed glass jar, UPC 642036010549
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0798-2015·2015-01-28

    Baroody Pickled Labneh Recalled for Undeclared Sorbic Acid

    Baroody Imports Inc. is recalling 9 cases of Baroody Pickled Labneh with Garlic in New York due to undeclared sorbic acid.

    Product
    Baroody Pickled Labneh with Garlic, Net Wt. 20 oz., (1 lb. 4 oz.), 575-g, in sealed glass jar, UPC 642036011164
    Category
    Food
    Distribution
    1 state
  • LowFDA (Drugs)·D-0376-2015·2015-01-28

    3M ESPE Clinpro 5000 Toothpaste Recalled for Missing Lot and Expiration Dates

    3M ESPE is recalling 19,728 tubes of Clinpro 5000 Anti-Cavity Toothpaste because the primary boxes are missing lot numbers and expiration dates.

    Product
    3M ESPE Clinpro 5000 (1.1% Sodium Flouride), Anti-Cavity Toothpaste, 4 oz tube (NDC 48878-3130-04), Rx Only, Manufactured for 3M ESPE Dental Products, St. Paul, MN 55144
    Category
    Drug
    Distribution
    Distributed nationwide