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.

6726–6750 of 9611

  • ModerateFDA (Devices)·Z-0855-2015·2014-12-31

    Unistrip Technologies Recalls Blood Glucose Test Strips for Labeling Changes

    Unistrip Technologies LLC is recalling 7,175 units of UniStrip1 Blood Glucose Test Strips because the company failed to submit a 510(k) for device labeling changes.

    Product
    UniStrip1, Blood Glucose Test Strips, 50 count box. The test strips are indicated for use by people with diabetes in their home as an aid to monitor the effectiveness of diabetes control.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Food)·F-0751-2015·2014-12-31

    Willy's Just Peachy Salsa Recalled for Missing Food Color Labeling

    Willy's Inc is recalling 1,944 containers of Just Peachy Salsa because the label failed to list FD & C Yellow #5, a food color additive.

    Product
    Willy's Just Peachy Salsa, packaged in 16-oz. plastic deli containers
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-0858-2015·2014-12-31

    Cyberonics VNS Therapy Generator Recalled for Incorrect Serial Number Labeling

    Cyberonics is recalling one VNS Therapy AspireHC Model 105 Generator distributed in Pennsylvania due to an incorrect serial number on the device label.

    Product
    Cyberonics VNS Therapy AspireHC, Model 105 Generator. The Cyberonics VNS Therapy System consists of the implantable VNS Therapy Generator, the VNS Therapy Lead, and the external programming system used to change the stimulation settings. Indicated for use as an adjunctive ther
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Food)·F-0739-2015·2014-12-24

    Ortega Taco Sauce Recalled for Potential Peanut and Almond Contamination

    B&G Foods is recalling Ortega Taco Sauce and other products because spice ingredients may contain undeclared peanuts and almonds.

    Product
    Ortega Taco Sauce - Medium 8 oz, UPC 39000-01892, 16 oz. UPC 39000-01894.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0738-2015·2014-12-24

    B&G Foods Recalls Ortega and Las Palmas Taco Sauces for Allergen Risk

    B&G Foods is recalling Ortega and Las Palmas Taco Sauce products because spice ingredients may contain undeclared peanuts and almonds.

    Product
    Taco Sauce - Mild sold under the following brands: 1. Ortega 8 oz, UPC 39000-00890, 16 oz. UPC 39000-01893; 2. Las Palmas 8 oz. UPC 41501-79890 and (Canada) 226 g. UPC 41501-79990.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0777-2015·2014-12-24

    Stryker Laparoscopic Scissors Recalled for Sterilization Parameter Errors

    Stryker Endoscopy is recalling 180,573 laparoscopic hook scissors because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 3MM INSERT, HOOK SCISSORS, 29CM, P/N 0250282049 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0729-2015·2014-12-24

    Whalen's Seafood Sauce Recalled for Undeclared Anchovies

    Whalen's Seafood & Burger Sauce is being recalled because it contains undeclared anchovies and has incomplete ingredient labeling.

    Product
    WHALEN'S SEAFOOD & BURGER SAUCE "HOT", NET WT. 8 OZ. (226 g) -- Whalen's Horseradish Products, LLC, PO Box 4700, Saratoga Springs, New York 12866
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0743-2015·2014-12-24

    HyVee Mozzarella Sticks Recalled for Undeclared Soy and Dyes

    Great American Appetizers is recalling HyVee Mozzarella Sticks because the product contains soy flour and dyes not listed on the label.

    Product
    Mozzarella cheese sticks are breaded Mozzarella Stick designed to be cooked in either the oven or a fryer. The package contains a clear inner plastic sealed bag with the food product, inside a cardboard larger carton. The net weight is 8 oz., and there are 12 units per case. Prod
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0728-2015·2014-12-24

    Kozy Shack Chocolate Pudding Recalled for Undeclared Milk

    Kozy Shack is recalling Simply Well Chocolate Pudding due to undeclared milk and incomplete labeling. The recall affects 1,774 cartons distributed across 20 states.

    Product
    KOZY SHACK SIMPLY WELL CHOCOLATE, NET WT 4 OZ. Product packed in brown carton box, 48 individual units x 4 OZ. Keep Refrigerated. Made in USA
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-0654-2015·2014-12-24

    Stryker Endoscopy Recalls Tissue Grasper Forceps Due to Sterilization Labeling Error

    Stryker Endoscopy is recalling 180,573 units of tissue grasper forceps because the instructions for use do not support two specific sterilization methods.

    Product
    PKG, GRASPER FORCEPS, TISSUE, P/N 0250080284. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0616-2015·2014-12-24

    Stryker Laparoscopic Reducers Recalled for Sterilization Parameter Errors

    Stryker Endoscopy is recalling 180,573 laparoscopic reducers because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 12.5/11MM - 5.5 REDUCER, P/N 0250080204. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0723-2015·2014-12-24

    Stryker 3.5mm Trocar Recalled for Sterilization Instructions Error

    Stryker Endoscopy is recalling 180,573 units of 3.5mm trocars because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 3.5MM TROCAR, PYRAMIDAL TIP, SHORT, P/N 0250080692 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) port
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0623-2015·2014-12-24

    Stryker Endoscopy Recalls Laparoscopic Instruments Due to Sterilization Documentation Errors

    Stryker Endoscopy is recalling 180,573 laparoscopic instruments because the instructions for use do not support specific sterilization methods.

    Product
    PKG, ROTATING HANDLE, RATCHET, INSULATED/SHAFT, P/N 0250080233. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0743-2015·2014-12-24

    Stryker Endoscopy Recalls Laparoscopic Manual Instruments Due to Sterilization Labeling Error

    Stryker Endoscopy is recalling 180,573 units of laparoscopic manual instruments because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 5MM INSERT, 45CM, DEBAKEY FORCEPS, P/N 0250080748 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0617-2015·2014-12-24

    Stryker Endoscopy Recalls Bullet Forceps Due to Sterilization Documentation Issues

    Stryker Endoscopy is recalling 180,573 units of Bullet Forceps because the instructions for use do not support specific sterilization methods.

    Product
    PKG, BULLET FORCEPS, TAPERED, SERRATED, SPOON, P/N 0250080041. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0775-2015·2014-12-24

    Stryker Endoscopy Recalls Laparoscopic Scissors Due to Sterilization Documentation Error

    Stryker Endoscopy is recalling 180,573 units of Metzenbaum scissors because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 3MM INSERT, METZENBAUM, CURVED, LONG SCISSORS, 29CM, P/N 0250282047 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio fr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0776-2015·2014-12-24

    Stryker Endoscopy Recalls Laparoscopic Scissors Due to Sterilization Documentation Error

    Stryker Endoscopy is recalling 180,573 units of laparoscopic scissors because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 3MM INSERT, PERITONEAL SCISSORS, 29CM, P/N 0250282048 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) p
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0733-2015·2014-12-24

    Stryker Endoscopy Recalls Laparoscopic Manual Instruments Due to Sterilization Documentation Error

    Stryker Endoscopy is recalling 180,573 laparoscopic manual instruments because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 5MM INSERT, ENDO GRASPER, 45CM, P/N 0250080726 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports wh
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0772-2015·2014-12-24

    Stryker Endoscopy Recalls Laparoscopic Manual Instruments Due to Sterilization Documentation Issues

    Stryker Endoscopy is recalling 180,573 laparoscopic manual instruments because the provided instructions for use do not support specific sterilization methods.

    Product
    PKG, 3MM INSERT, STRAIGHT NEEDLEHOLDER, 20CM, P/N 0250282014 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0673-2015·2014-12-24

    Stryker Laparoscopic Forceps Recalled for Sterilization Instructions Error

    Stryker Endoscopy is recalling 180,573 units of atraumatic forceps because the instructions for use do not support specific sterilization methods.

    Product
    PKG, ATRAUMATIC FORCEPS, DOUBLE ACTION, P/N 0250080311. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) port
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0703-2015·2014-12-24

    Stryker Endoscopy Recalls 5mm Metzenbaum Scissors Due to Sterilization Labeling Error

    Stryker Endoscopy is recalling 180,573 units of 5mm Metzenbaum Scissors because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 5MM INSERT, ENDO METZENBAUM SCISSORS, CURVED 45CM, P/N 0250080575 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio freq
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0684-2015·2014-12-24

    Stryker Endoscopy Recalls Babcock Forceps Due to Sterilization Documentation Errors

    Stryker Endoscopy is recalling 180,573 units of Babcock Forceps because the instructions for use do not support specific sterilization methods.

    Product
    PKG, BABCOCK FORCEPS, P/N 0250080321. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them
    Category
    Medical Device
    Distribution
    Distributed nationwide