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.

Which agencies issued them

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.

8601–8625 of 9611

HighFDA (Food)·F-1648-2013·2013-07-17
Christian Cheese Vegetable Cheddar Recalled for Undeclared Soy Ingredients
Christian Cheese, LLC is recalling Vegetable Cheddar cheese sold in Colorado and Oklahoma due to undeclared soy lecithin and soybean oil.
Product
Christian Cheese Vegetable Cheddar Made in Kingfisher, Oklahoma (405-375-6711) Ingredients: Pasteurized Milk, Culture, Rennet, Salt, Onion, Garlic, Basil, Red Bell Pepper, Black Pepper, Tomato, Vinegar, Parsley, Ginger, and Rosemary. 1 unit weighing approximately 0.6 lbs and p
Category
Food
Distribution
2 states
HighFDA (Food)·F-1652-2013·2013-07-17
Christian Cheese Horseradish Cheddar Cheese Recalled for Undeclared Soy
Christian Cheese, LLC is recalling Horseradish Cheddar Cheese due to undeclared soy lecithin and soybean oil. The product was distributed in Colorado and Oklahoma.
Product
Christian Cheese Horseradish Cheddar Cheese Made in Kingfisher, Oklahoma (405-375-6711) Ingredients: Pasteurized Milk, Culture, Vegetable Rennet, Salt, and Horseradish. 1 unit weighing approximately 0.6 lbs and plastic vacuum packed in plastic. 1 case is approximately 32 units
Category
Food
Distribution
2 states
HighFDA (Food)·F-1619-2013·2013-07-17
Los Milagros Green Corn Tamales Recalled for Undeclared Milk Allergen
Los Milagros Tortilleria is recalling Green Corn Tamales because they contain an undeclared milk allergen from Monterey Jack cheese.
Product
Milagros Green Corn Tamales, packaged in plastic in quantities of one dozen
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-1675-2013·2013-07-17
AngioDynamics RITA Main Cable Recalled for Incorrect Instructions for Use
AngioDynamics is recalling 13 RITA Main Cables because they contain incorrect Instructions for Use. The cables are used with RITA RF Generators and electrosurgical devices.
Product
AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables are indicated for use with the RITA RF Generators and RITA electrosurgical devices.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1676-2013·2013-07-17
Zimmer Recalls Mislabelled Shoulder Trial Stem Devices
Zimmer, Inc. is removing one lot of Bigliani/Flatow Humeral Provisional Stems because 14mm devices were incorrectly etched and packaged as 12mm.
Product
Bigliani/Flatow¿ The Complete Shoulder Solution, Humeral Stem Provisional 12mm x 170mm This reusable trial device is used in orthopaedic joint replacement and is specific to the replaced joint (e.g. hip, knee, shoulder, ankle, elbow). It can be made of metal or plastic.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1667-2013·2013-07-17
Bryan Medical Recalls Mislabeled Pediatric Tracheostomy Tubes
Bryan Medical Inc is recalling 5 units of Tracoe Mini 3.0mm pediatric tracheostomy tubes because they were mislabeled as smaller infant tubes.
Product
Tracoe Mini 3.0mm Tube, for pediatric use. Pediatric tracheostomy tube used to provide safe airway access.
Category
Medical Device
Distribution
2 states
LowFDA (Devices)·Z-1671-2013·2013-07-17
Boston Scientific Recalls Rigiflex Balloon Dilator for Incorrect Expiration Date
Boston Scientific is recalling 91 units of the Rigiflex Single-Use Achalasia Balloon Dilator because they were labeled with an incorrect expiration date.
Product
RigiflexTM 11 Single-Use Achalasia Balloon Dilator, Material Number (UPN) M00554510 Product Usage: The Boston Scientific Corporation RigiflexTM II Single- Use Achalasia Balloon Dilator is indicated for dilatation of the cardia in patients with achalasia.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1577-2013·2013-07-10
Cheryls Peanut Butter Cookies Recalled for Undeclared Allergen
Cheryls is recalling Fudge Buttercream Frosted Peanut Butter cookies because some were packaged in Cinnamon Pumpkin wrappers, creating an undeclared peanut allergen risk.
Product
Fudge Buttercream Frosted Peanut Butter cookies, some of which were mislabeled by being wrapped in Buttercream Frosted Cinnamon Pumpkin cookie wrappers, 1.6oz (45g) in size, 1 cookie per package, 100 cookies per case.
Category
Food
Distribution
47 states
ModerateFDA (Devices)·Z-1619-2013·2013-07-10
ConMed Linvatec Recalls Genesys Cross FT Suture Anchors Due to Incorrect Suture Color
ConMed Linvatec is recalling 60 units of Genesys Cross FT Suture Anchors because incorrect blue/white sutures were used instead of the specified type.
Product
GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Hi-FI Registered Trade Mark Sutures Rx Only STERILE EO CONMED LINVATEC REF CFBC-4502. Reattachment of soft tissue to bone in orthopedic surgical procedures
Category
Medical Device
Distribution
6 states
LowFDA (Devices)·Z-1662-2013·2013-07-10
BD MAX Instrument Recall for Non-Compliant Electrical Power Module
Becton Dickinson is recalling 71 BD MAX instruments because the installed electrical power module does not meet industry standards as labeled.
Product
BD MAX Instrument, catalog #441916 Product Usage: The BD MAX System, used in conjunction with the appropriate extraction kits and reagents is capable of automated amplification and detection of target nucleic acid sequences for use in clinical, industrial, and research setti
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1588-2013·2013-07-03
Philips CT Scanners Recalled for Patient Selection and Scan Safety Issues
Philips Medical Systems is recalling 50 CT scanners due to a software defect that can cause incorrect patient names to appear on exam pages and allow clinical scans to start during anti-virus scans.
Product
Brilliance CT 64, Ingenuity CT, Ingenuity Core, and Ingenuity Core128 scanners are whole body Computed Tomography X-ray systems. Produce cross-sectional images of the body by computer reconstruction of x-ray transmission.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1587-2013·2013-07-03
U-systems Recalls Soma v Automated Breast Ultrasound System for Labeling Error
U-systems Inc is recalling three Soma v Automated Breast Ultrasound Systems because the user manuals incorrectly list the indication for use of a different product model.
Product
Soma v Automated Breast Ultrasound System (ABUS), Automated Breast Ultrasound. Indicated as an adjunct to mammography for breast cancer screening.
Category
Medical Device
Distribution
2 states
ModerateFDA (Devices)·Z-1599-2013·2013-07-03
ConBio Recalls Multilite Dye Handpieces for Display Identification Inconsistency
ConBio is recalling 12 Multilite Dye Handpieces for the RevLite SI Laser due to an electronic display inconsistency that may confuse users.
Product
Multilite Dye Handpieces, an optional accessory of the RevLite SI Laser. The Revlite SI laser is intended for General Dermatology, Dermatologic and General Surgical Procedures. Which includes treatments such as tattoo removal, pigmented lesion removal, removal or lightening of
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1551-2013·2013-07-03
Enzyme Solutions Formula 29 Recalled for Labeling Error
Enzyme Formulations, Inc. is recalling 256 bottles of Enzyme Solutions Formula 29 due to a manufacturing labeling error that resulted in incorrect contents.
Product
Enzyme Solutions, A Dietary Supplement, Formula 29, 8 oz. (226.8g), UPC Code 697706041408. Distributed by: Enzyme Formulations, Inc., Madison, Wisconsin, 53719.
Category
Food
Distribution
28 states
ModerateFDA (Drugs)·D-620-2013·2013-07-03
Kareway Recalls Pure-Aid Allergy Relief Caplets Due to Labeling Error
Kareway Products Inc. is recalling Pure-Aid Allergy Relief caplets because the foil label incorrectly lists Chlorpheniramine instead of Diphenhydramine.
Product
Pure-Aid Allergy Relief, Diphenhydramine HCL Caplets, 25 mg, 20 caplets, Exclusively distributed by: Kareway Products Inc., Compton, CA --- UPC 8 56023 00158 2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1611-2013·2013-07-03
Terumo Pinnacle Destination Peripheral Guiding Sheath Recalled for Labeling Error
Terumo Medical Corporation is recalling 20 units of Pinnacle Destination Peripheral Guiding Sheaths because they were incorrectly labeled with extended expiration dates.
Product
Pinnacle¿ Destination¿ Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction of interventional and diagnostic devices into the human vasculature.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-623-2013·2013-07-03
Baxter Recalls 0.9% Sodium Chloride Injection Due to Barcode Labeling Error
Baxter Healthcare is recalling 317,280 bags of 0.9% Sodium Chloride Injection because the barcode may incorrectly identify the product as 100 mL instead of 50 mL.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1564-2013·2013-07-03
Medtronic Launcher Guiding Catheter Recalled for Labeling Errors
Medtronic is recalling 24 units of Launcher Guiding Catheters because the packaging labels do not accurately reflect the catheters inside.
Product
Medtronic, Launcher Guiding Catheter, Model # LA8EBU45SH, Lot # 0006722866, 8F and Model # LA6IMAD, Lot # 0006724224, 6F Product Usage: The Medtronic Guiding Catheter is designed to provide a pathway through which therapeutic devices are introduced. The guiding catheter is i
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1612-2013·2013-07-03
Terumo Glidesheath Recalled for Incorrect Expiration Date Labeling
Terumo Medical Corporation is recalling 550 units of Glidesheath products due to incorrect expiration date labeling.
Product
Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060. Used to facilitate placing a catheter through the skin into a vein or artery.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1596-2013·2013-07-03
STERIS Recalls Quick Connects for Labeling Updates
STERIS Corporation is recalling four Quick Connect products to update labeling and remove obsolete device models.
Product
Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation, Mentor, OH 44060 QLC1677E, QRC1699E, QPC1721E and QFC1683E contain processing instructions, a Quick Reference Wall Chart and a flow unit. The flow unit consists of a Quick Reference Card, tubing, teth
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1568-2013·2013-07-03
Integra LifeSciences Recalls Ascension CMC Saddle Due to Labeling Discrepancies
Integra LifeSciences is recalling 467 Ascension CMC Saddle implants because the US Instruction for Use contains content discrepancies compared to the FDA-cleared version.
Product
CMC Saddle Product Usage: The Ascension CMC is intended to resurface the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteo-arthritis, or post-fracture deformation or bone loss which present as either a painful, unstable thumb, o
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·13V277000·2013-06-28
Starcraft Recalls 2014 Launch Ultra Lite Trailers Due to Labeling Error
Starcraft is recalling 36 model year 2014 Launch Ultra Lite travel trailers because incorrect cargo capacity labels may lead to tire overloading and failure.
Product
STARCRAFT — STARCRAFT LAUNCH ULTRA LITE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1533-2013·2013-06-26
Lightlife Veggie Burgers Recalled for Undeclared Milk Allergen
Conagra is recalling Lightlife Farmer's Market Veggie Burgers because packaging may contain milk-containing products, and the milk allergen is not declared on the label.
Product
Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed By: Lightlife Foods, Turners Falls, MA. Case UPC Code: 20043454805252
Category
Food
Distribution
33 states
ModerateFDA (Devices)·Z-1544-2013·2013-06-26
SybronEndo Elements Obturation Unit Recalled for Missing Safety Label
SybronEndo is recalling 3,615 Elements Obturation Units because a required Canadian safety caution label was accidentally omitted from the device and its power cord.
Product
SybronEndo Elements Obturation Unit; REF 973-0322; SN 91-1234; 2005-10; SybronEndo, 1332 S. Lone Hill Ave. Glendora, CA 91740; EU Rep: Kerr Italia, S.r.l, Via Passanti, 332, 1-84018 Scafati (SA), Italy The intended use of the Elements Obturation Unit and Replacement A/C Power
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1549-2013·2013-06-26
Aperio ScanScope Systems Recalled for Incorrect User Guide Labeling
Aperio Technologies is recalling 364 ScanScope systems because user guides incorrectly claim FDA clearance for diagnostic use, when the devices are for research only.
Product
Aperio ScanScope System. Aperio ScanScope Models, XT, AT, AT Turbo, CS and CSO. Automated digital slide creation and viewing device. It is intended to create and view electronic image files representative of tissue specimens fixed to glass slides.
Category
Medical Device
Distribution
Distributed nationwide