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.

3001–3025 of 9607

  • HighFDA (Food)·F-0761-2019·2019-02-06

    Glass Onion Catering Recalls Hummus and Quinoa Wraps Due to Undeclared Soy

    Atherstone Foods, Inc. dba Glass Onion Catering is recalling 114 units of Hummus & Quinoa Tabouleh Wraps because mayonnaise containing soy was used in error, and the product label does not declare soy as an allergen.

    Product
    greens & Grains Hummus & Quinoa Tabouleh Wrap with lemon tahini dressing: Perishable: Keep Refrigerated Plastic container with tamper proof hinged lid Use by 12/19/18 Incorrect dressing was used: Label states: Dressing: Tahini (ground sesame seeds), Lemon Juice, Water,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0780-2019·2019-02-06

    Sysco Classic Liquid Margarine Recalled for Mislabeled Soy Lecithin

    Ventura Foods LLC is recalling Sysco Classic Liquid Margarine because the interior packaging misidentifies the product as canola oil, failing to declare soy lecithin.

    Product
    Sysco Classic Liquid Margarine; 2 x 17.5 lb. plastic containers; 99961WFS
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0774-2019·2019-02-06

    Wilson-Cook Medical Recalls Mislabelled Captura Serrated Biopsy Forceps

    Wilson-Cook Medical is recalling 8 units of Captura Serrated Biopsy Forceps in France, Ireland, and Japan due to mislabeling.

    Product
    COOK MEDICAL Captura SERRATED BIOPSY FORCEPS WITH SPIKE,2.4 mm, 230 cm, with Spike, DBF-2.4SN-230SP-20-S
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0775-2019·2019-02-06

    Wilson-Cook Medical Recalls Mislabeled Captura Serrated Forceps

    Wilson-Cook Medical is recalling 6 units of Captura Serrated Forceps due to mislabeling that swapped spike and no-spike models.

    Product
    COOK MEDICAL Captura SERRATED LARGE FORCEP-NO SPIKE, 2.4 mm, 230 cm, DBF-2.4SL- 230-20-S
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-0777-2019·2019-02-06

    Riverpoint Medical Recalls 18G Brachy Grids for Incorrect CE Labeling

    Riverpoint Medical is recalling 443 units of 18G Brachy Grids because they are labeled with a CE mark despite not being approved in the European Union.

    Product
    RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style, REF RPG-18 Product Usage: The Riverpoint Brachytherapy Grid is used during Brachytherapy procedures to assist with the precise insertion of the needle or other probes. The Riverpoint Brachytherapy Grid is placed against the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0762-2019·2019-02-06

    Edwards Lifesciences Recalls Swan Ganz Catheters Due to Lumen Assembly Error

    Edwards Lifesciences is recalling 277 Swan Ganz Thermodilution Catheters because incorrect lumen assembly causes reversed pressure readings.

    Product
    Edwards Lifesciences Swan Ganz Thermodilution Catheter, REF131F 7J Product Usage: The Swan-Ganz Thermodilution Catheter provides a diagnostic tool for physicians to rapidly determine hemodynamic pressures and cardiac output when used with a compatible cardiac output computer.
    Category
    Medical Device
    Distribution
    0 states
  • HighUSDA FSIS·011-2019·2019-02-02

    Taylor Farms Recalls Chicken Products Due To Misbranding And Undeclared Allergens

    Taylor Farms TX, Inc. is recalling approximately 2,100 pounds of chicken products incorrectly labeled as Chile Relleno due to misbranding and undeclared wheat allergens.

    Product
    Taylor Farms TX, Inc. — Taylor Farms TX, Inc. Recalls Chicken Products Due To Misbranding And Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0386-2019·2019-01-30

    Bound Tree Medical Recalls Curaplex Epi Kits Due to Incorrect Instructions

    Bound Tree Medical is recalling 339 Curaplex Epi Kits because the instructions recommend an unapproved epinephrine dosage for young children.

    Product
    Curaplex Epi Kit NOT FOR IV USE, #8600-01120, Epi-Safe Kit 8600-01 120 contains:2 Safety-LOK Syringe, TB, 1cc w/ needle, 25 ga x5/8 , 2 Vials of epinephrine, 1mg/1mL, 4 Alcohol prep pads, 2 Adhesive bandages, 1 x 3 1 Epi Generic Injection. Rx Only. Distributed by Sarnova HC, L
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0384-2019·2019-01-30

    Recall of Curaplex Epi Safe Kits Due to Incorrect Epinephrine Instructions

    Bound Tree Medical is recalling Curaplex Epi Safe Kits because the instructions recommend an unapproved epinephrine dosage for young children.

    Product
    curaplex Epi Safe Kit, 8600-01101, contains:" 1ml Vial of Epinephrine " 1 Epi-Safe Syringe " 1 Safety Needle " 2 Alcohol Prep Pads " 1 Adhesive Dressing " 1 Insert, Rx Only. Distributed by Sarnova HC, LLC s family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc., Eme
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0383-2019·2019-01-30

    Bound Tree Medical Recalls Epi Safe Kits Due to Incorrect Instructions

    Bound Tree Medical is recalling Epi Safe Administration and Training Kits because the instructions recommend an unapproved epinephrine dosage for young children.

    Product
    curaplex Epi Safe Administration and Training Kits, #8600-01100, Contains: 2 Epi Safe Administration Kit (8600-01101), 1 Epi Safe Training Kit (8600-01102), Rx Only, Distributed by Sarnova HC, LLC s family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc., Emergency Me
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0385-2019·2019-01-30

    Bound Tree Medical Recalls Curaplex Epi Safe Training Kits Due to Labeling Errors

    Bound Tree Medical is recalling 2,654 Curaplex Epi Safe training kits because the instructions recommend an unapproved epinephrine dosage for young children.

    Product
    Curaplex Epi Safe Kit, 8600-01102 TRAINING ONLY, Rx Only, Distributed by Sarnova HC, LLC s family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc., Emergency Medical Products, Inc. & Tri-anim Health Services, Inc. 5000 Tuttle Crossing Blvd. Dublin, OH 43016
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0430-2019·2019-01-30

    Heparin Injectable Solution Recalled for Incorrect Concentration Labeling

    Advanced Pharma Inc. is recalling Heparin Injectable Solution because the label incorrectly states the concentration as 50 mg/50 mL instead of 50 Units/50 mL.

    Product
    HEPERAIN 50 mg/50 mL (1mg/mL) Injectable Solution, Heparin Sodium 0.45% Sodium Chloride QS Heparin 50 Units 50 mL, Sterile single use syringe, Avella of Houston an FDA Registered 503B Outsourcing Facility 9265 Kirby Dr. Houston, TX 77054 (877) 794-0404 ---- NDC: 42852-725-65
    Category
    Drug
    Distribution
    2 states
  • LowFDA (Drugs)·D-0391-2019·2019-01-30

    Sun Pharmaceutical Recalls Loperamide Hydrochloride Tablets Due to Labeling Error

    Sun Pharmaceutical Industries is recalling 5,040 cartons of Loperamide Hydrochloride 2 mg tablets because the carton front and side panels display conflicting caplet counts.

    Product
    LOPERAMIDE HYDROCHLORIDE — LOPERAMIDE HYDROCHLORIDE (LOPERAMIDE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    1 state
  • CriticalUSDA FSIS·008-2019·2019-01-28

    Perdue Recalls Chicken Nuggets Due to Undeclared Milk Allergen

    Perdue Foods is recalling refrigerated chicken nuggets because they contain milk, a known allergen, that is not listed on the label.

    Product
    PERDUE FOODS, LLC. — Perdue Foods, LLC Recalls Refrigerated Fun Shapes Chicken Breast Nuggets Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-0747-2019·2019-01-23

    Ethicon Recalls PERMA-HAND Silk Sutures Due to Labeling Mismatch

    Ethicon is recalling 840 units of PERMA-HAND Silk Sutures because the product inside the packaging does not match the size or type indicated on the label.

    Product
    PERMA-HAND Silk Suture Size 5, Black 30" (75cm) Double Armed LR Needles, Product Code 485T Product Usage: PERMA-HAND* suture is indicated for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic and neurological procedures.
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-0746-2019·2019-01-23

    DeRoyal Enteral Safe Feed Tube Recall Due to Incorrect Sizing

    DeRoyal Industries is recalling 200 Enteral Safe Feed Tubes labeled as 6.5 FR but containing 5 FR tubes. The recall covers units distributed to Texas and Utah.

    Product
    DeRoyal(R) Enteral Safe Feed Tube, REF 54-2465 A Nasogastric/Oralgastric enteral feeding tube. The MED-RX Feeding Tube is intended to be used for nasogastric/oralgastric enteral feeding as directed by a physician
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0723-2019·2019-01-23

    Arrow Pediatric Central Venous Catheter Recalled for Incorrect Labeling

    Arrow International Inc. is recalling specific lots of pediatric central venous catheters because the lidstock labels list incorrect priming volumes and flow rates.

    Product
    Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm, Reference # CS-12402 The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring centra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0371-2019·2019-01-23

    Recall of Curaplex Epi Safe Kits Due to Expired Epinephrine Vials

    Bound Tree Medical is recalling 84 Curaplex Epi Safe Administration and Training Kits because the epinephrine vials inside expired in December 2018, despite the outer label showing January 2020.

    Product
    curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit contains 2 Epi Safe Administration Kit (8600-01101) and 1 Epi Safe Training Kit (8600-01102), Rx Only. Distributed by Sarnova HC, LLC's family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc., Emerge
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0728-2019·2019-01-23

    Waldemar Link BiMobile UHMWPE Liner Recalled for Incorrect Internal Labeling

    Waldemar Link is recalling 30 BiMobile UHMWPE Liners because internal labeling may contain incorrect part numbers, risking errors in patient records.

    Product
    BiMobile UHMWPE Liner: ID-28mm/OD-50mm, Reference Number 184-260/02 The LINK BiMobile Dual Mobility System is indicated for patients with mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures. The device is intend
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0725-2019·2019-01-23

    Canadian Hospital Specialties Recalls Pediatric Polyurethane Feeding Tubes Due to Labeling Error

    Canadian Hospital Specialties is recalling 750 pediatric polyurethane feeding tubes because they may be packaged with a 5FR tube instead of the labeled 6.5FR size.

    Product
    MED-RX POLYURETHANE FEEDING TUBE For Pediatric Use with Orange Radioplaque Stripe and Enteral Connector, 6.5Fr X 24" (60cm), REF 54-2465-R Product Usage: A Nasogastric/Oralgastric enteral feeding tube. The MED-RX Feeding Tube is intended to be used for nasogastric/oralgastri
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0729-2019·2019-01-23

    Waldemar Link Recalls BiMobile UHMWPE Liners Due to Labeling Errors

    Waldemar Link is recalling 31 BiMobile UHMWPE Liners because internal labels may contain incorrect part numbers, risking errors in patient records.

    Product
    BiMobile UHMWPE Liner: ID-28mm/OD-54mm, Reference Number 184-260/04 The LINK BiMobile Dual Mobility System is indicated for patients with mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures. The device is intend
    Category
    Medical Device
    Distribution
    8 states
  • LowFDA (Drugs)·D-0379-2019·2019-01-23

    Bound Tree Medical Recalls Curaplex Epi Safe Kits Due to Labeling Errors

    Bound Tree Medical is recalling 747 Curaplex Epi Safe Kits because they are incorrectly labeled with an expiration date of May 2018 instead of May 2019, and the syringe component lacks 510(k) clearance.

    Product
    Curaplex Epi Safe Kit, Rx Only, contains: 1mL Vial of Epinephrine, 1 Epi-Safe Syringe, 1 Safety needle, 2 Alcohol Prep Pads,1 Adhesive Dressing, 1 Insert. Distributed by Sarnova, HC. LLC's family companies: Bound Tree Medical. LLC, Cardio Partners, Inc., Emergency Medical Product
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0709-2019·2019-01-16

    Biomet DVR Crosslock Screws Recalled Due to Incorrect Length Labeling

    Zimmer Biomet is recalling two lots of Biomet DVR Crosslock Screws because the actual screw lengths do not match the labels.

    Product
    Biomet DVR Crosslock Screws- 2.7mm x18mm, Sterile ITEM 131827118 Product Usage: Usage: The system is intended for stabilization and fixation of small bone fragments in fresh fractures, revision procedures, joint fusion and reconstructions (osteotomies) of small bones of th
    Category
    Medical Device
    Distribution
    0 states