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.

6851–6875 of 9611

  • ModerateFDA (Devices)·Z-0765-2015·2014-12-24

    Stryker Endoscopy Recalls 180,573 Cobra Grasper Instruments Due to Sterilization Labeling

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

    Product
    PKG, 3MM INSERT, COBRA GRASPER, 20CM, P/N 0250282007 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
  • ModerateFDA (Devices)·Z-0713-2015·2014-12-24

    Stryker Laparoscopic Needle Holder Recall Due to Sterilization Documentation Error

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

    Product
    PKG, 5MM SHAFT, NEEDLE HOLDER, STRAIGHT, 45CM, P/N 0250080588 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
  • LowFDA (Devices)·Z-0755-2015·2014-12-24

    Stryker Endoscopy Recalls Laparoscopic Instruments Due to Sterilization Labeling Error

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

    Product
    PKG, 5MM MULTI-FUNCTION PEEK HANDLE, P/N 0250181106 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
  • LowFDA (Devices)·Z-0814-2015·2014-12-24

    Aesculap Miethke Shunt System Recalled for Missing Patient Labels

    Aesculap Inc. is recalling four units of the Miethke Shunt System miniNAV Valve due to missing patient labels. No patient injuries have been reported.

    Product
    Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of the brain into the peritoneum.
    Category
    Medical Device
    Distribution
    2 states
  • LowFDA (Drugs)·D-0302-2015·2014-12-24

    Eisai Recalls Belviq Tablets Due to Missing or Illegible Labels

    Eisai Inc. is recalling 121,680 bottles of Belviq (Lorcaserin HCl) 10 mg tablets because some bottles may lack labels or have illegible lot and expiry dates.

    Product
    BELVIQ¿ (Lorcaserin HCl) Tablets, 10 mg, 60-count bottle, Rx only, Manufactured by: Arena Pharmaceuticals, GmbH, Zofingen, Switzerland, Distributed by: Elsai Inc., Woodcliff, NJ 07677 NDC 62856-52960.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0634-2015·2014-12-24

    Stryker Laparoscopic Forceps Recalled for Sterilization Instructions Error

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

    Product
    PKG, OP-VIOPSY FORCEPS, SPOON JAW, P/N 0250080246. 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
  • LowFDA (Devices)·Z-0826-2015·2014-12-24

    Teleflex Recalls Weck Hemoclip Ligating Clips Due to Labeling Error

    Teleflex Medical is recalling 3,180 units of Weck Hemoclip Ligating Clips because manufacturing and expiration dates were transposed on the packaging labels.

    Product
    WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·088-2014·2014-12-23

    DaBecca Sliced Uncured Apple Smoked Bacon Recalled for Misbranding

    DaBecca is recalling approximately 3,450 pounds of sliced uncured apple smoked bacon because the labels lacked the USDA mark of inspection.

    Product
    DaBecca LLC — Recall Notification Report 088-2014 (DaBecca Sliced Uncured Apple Smoked Bacon)
    Category
    Food
    Distribution
    2 states
  • LowUSDA FSIS·086-2014·2014-12-22

    Abe's Finest Meats Recalls Hickory Smoked Sliced Bacon for Misbranding

    Abe's Finest Meats is recalling approximately 80,050 pounds of hickory smoked sliced bacon because the ingredient sodium nitrite is not declared on the label.

    Product
    Recall Notification Report 086-2014 (Hickory Smoked Sliced Bacon)
    Category
    Food
    Distribution
    2 states
  • ModerateUSDA FSIS·085-2014·2014-12-19

    Katadyn Recalls Spicy Sausage Pasta Due to Pork Mislabeling

    Katadyn North America Foods is recalling 2,719 pounds of Spicy Sausage Pasta because the label lists beef but the product contains pork.

    Product
    Katadyn North America Foods, LLC. — Recall Notification Report 085-2014 (Spicy Sausage Pasta)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0527-2015·2014-12-17

    Alcon Single-Use Iris Bipolar Forceps Recalled for Lack of Sterilization

    Alcon Research, Ltd. is recalling single-use iris bipolar forceps labeled as sterile but not sterilized prior to shipment.

    Product
    Alcon Single-Use Curved Jewelers/Iris Bipolar Forceps REF 8065129101 Sterile RX only; Alcon Single-Use Straight/Iris Bipolar Forceps REF 8065129501 Sterile RX only. Usage: Electrosurgical instrument for ophthalmic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0708-2015·2014-12-17

    Whole Foods Market Vegan Pumpkin Pie Recalled for Undeclared Walnuts

    Whole Foods Market is recalling 1,144 vegan pumpkin pies because they contain walnuts that are not listed on the label.

    Product
    Whole Foods Market 9 inch Vegan Pumpkin Pie (32 oz) and 1/2 Vegan Pumpkin Pie (15 oz), packaged in both clear, clamshell packaging and brown, Kraft paper boxes. Distributed by Whole Foods Market. UPCs 24917101099 and 24917300699.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0623-2015·2014-12-17

    Cheesecake Royale Recalls Carrot Cakes Due to Undeclared Walnuts

    Cheesecake Royale is recalling 8-pound carrot cakes because they contain undeclared walnuts. The ingredient label lists pecans but fails to disclose the presence of walnuts.

    Product
    CARROT CAKE, Weight: 8 lbs. (112 oz.) - 3.6 kg, UPC#85538300025
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0704-2015·2014-12-17

    Schwartz Brothers Everything Bagels Recalled for Undeclared Milk Allergen

    Schwartz Brothers Bakery is recalling 321 bags of Everything Bagels because the product contains milk but the label does not declare it.

    Product
    "Everything Bagels" product is packed in a clear 4-pack plastic bag, with visible image of cheese melted on top of the bagels. This product has the UPC number 7 17887 23121 1. The product is labeled in parts: "***Everything Bagels***Net Wt. 16 oz (1 lb) 454 g***Produced By S
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0624-2015·2014-12-17

    Cheesecake Royale Recalls Rocky Road Brownies for Undeclared Wheat

    Cheesecake Royale, Inc. is recalling Rocky Road Brownies because the product contains undeclared wheat, posing a risk to individuals with wheat allergies or celiac disease.

    Product
    Rocky Road Brownies, Net Wt. (5 lbs), Item # 041, UPC#85538300041
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0573-2015·2014-12-17

    Arrow Recalls Nerve Block Components Due to Labeling Inconsistency

    Arrow International Inc is recalling specific lots of Continuous Nerve Block Components because the packaging incorrectly identifies the needle gauge. No injuries or illnesses have been reported.

    Product
    Arrow Nerve Block Component, Product Code: AB-18040-N: Permits placement of catheters next to nerves and nerve plexuses for continuous nerve block anesthesia or analgesia techniques for periods not exceeding 72 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0581-2015·2014-12-17

    Conformis iTotal CR G2 Knee Replacement System Recalled for Incorrect Serial Numbers

    ConforMIS, Inc. is recalling one unit of the iTotal CR G2 Knee Replacement System due to an incorrect serial number on the tibial insert packaging.

    Product
    Conformis iTotal CR G2 Knee Replacement System Catalog/Model #: M57250600010 Intended for use as a total knee replacement in patients with knee joint pain and disability.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0705-2015·2014-12-17

    Orrington Farms Chicken Broth Base Recalled for Mislabeling

    Kent Precision Foods Group is recalling Orrington Farms Chicken Flavored Broth Base due to incorrect labeling on beef-flavored product.

    Product
    Chicken flavored broth base and seasoning, low sodium sold under the Orrington Farms brand in 5 oz. plastic jars.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0528-2015·2014-12-17

    Concentric Medical Recalls Trevo Pro 4 Stent Retrievers Due to Labeling Error

    Concentric Medical is recalling 10 units of Trevo Pro 4 Stent Retrievers because they were shipped with non-U.S. instructions for use that did not align with U.S. indications.

    Product
    Trevo Pro 4 Stent Retriever, Model number 80021; U.S. Indications for use: The Trevo Retriever is intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke within 8 hours of symptom onset. Patients who are ineligible
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0525-2015·2014-12-17

    Concentric Medical Recalls Distal Access Catheters Due to Incorrect Labeling

    Concentric Medical is recalling 87 Distal Access Catheters because they were shipped with Directions for Use containing instructions for aspiration, which are only approved outside the US.

    Product
    Distal Access Catheter: Model Numbers: 90121, 90130, 90131, 90160. The Distal Access Catheter is intended for use in facilitating the insertion and guidance of an occlusion catheter, infusion catheter or other appropriate microcatheter into a selected blood vessel in the peri
    Category
    Medical Device
    Distribution
    17 states
  • LowFDA (Drugs)·D-0291-2015·2014-12-17

    Sandoz Recalls Fluoxetine Capsules Due to Illegible Logo

    Sandoz Inc. is recalling one lot of Fluoxetine Capsules because the logo on the capsules is illegible.

    Product
    Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 Capsules, Sandoz Inc Princeton, NJ 08540 NDC 0781-2822-01
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-0496-2015·2014-12-10

    Cure Medical Recalls Pediatric Urinary Catheters Due to Labeling Error

    Cure Medical is recalling pediatric urinary catheters because some boxes are mislabeled as size 8 but contain size 10 catheters, posing a risk of injury.

    Product
    Pediatric, 10Fr, Intermittent Urinary Catheters Model: P10 Pouch Label UPC (P10) *+M405P100C* Intermediate Box Label UPC (P10) *+M405P103F* Carton Label UPC (P10) *+M405P105H* The product is distributed individually or in intermediate boxes containing 30 individual, steril
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·084-2014·2014-12-10

    Real Foods LLC Recalls Chef Salads Due To Undeclared Anchovies

    Real Foods LLC is recalling Chef Salad with Ham and Turkey because the product contains anchovies, an undeclared allergen, and is mislabeled with the wrong dressing.

    Product
    Washington Firm Recalls Chef Salads with Ham and Turkey Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0487-2015·2014-12-10

    Beevers Cannulaide Model 101 Recalled for Incorrect Labeling

    Beevers Manufacturing recalled 393 units of Cannulaide Model 101 because the product was packed and labeled as Model 102.

    Product
    Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied under and over the nose o
    Category
    Medical Device
    Distribution
    Distributed nationwide