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.

7301–7325 of 9611

ModerateFDA (Devices)·Z-1851-2014·2014-07-02
Teleflex Medical Recalls RUSCH LaserTube Tracheal Tubes for Missing Latex Warning
Teleflex Medical is recalling RUSCH LaserTube tracheal tubes because the label failed to print a specific caution statement regarding natural rubber latex.
Product
RUSCH, LaserTube (Rubber), Laser Resistant Tracheal Tube, cuffed, Teleflex Medical, Willy-Rusch, GmbH. A tracheal tube is a device inserted into a patient's trachea via the nose or mouth and used to maintain an open airway.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1863-2014·2014-07-02
Philips Recalls Ingenia 1.5T MRI Systems Due to Incorrect Hardware
Philips Medical Systems is recalling 33 Ingenia 1.5T MRI systems because incorrect M10 nuts were installed on the rear cover set.
Product
Ingenia 1.5T R5, magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1928-2014·2014-07-02
Alere Triage BNP Calibrators Recalled Due to Mislabeling
Alere San Diego is recalling BNP calibrators because a Level 5 bottle contains Level 4 material, causing calibration failures.
Product
Alere Triage BNP Calibrators for the Beckman Coulter Access Family of Immunoassay Systems, Model No. 98202 The Alere Triage BNP test is intended for use with the Beckman Coulter Access Family of Immunoassay Systems for the In Vitro quantitative measurement of B-type natriureti
Category
Medical Device
Distribution
Distributed nationwide
ModerateNHTSA·14V406000·2014-07-02
Ford Recalls 2014 Transit Connect Vehicles for Missing Brake Fluid Label
Ford is recalling 2014 Transit Connect vehicles because the brake reservoir cap may lack required text identifying the correct brake fluid. This non-compliance could lead to incorrect fluid usage and brake system damage.
Product
FORD — FORD TRANSIT CONNECT
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1847-2014·2014-07-02
Baxter Abacus 3.1 Pharmacy Calculator Software Field Correction
Baxter is correcting a software error in Abacus 3.1 that may display protein levels 1,000 times lower than actual when using Clinimix 4.25110.
Product
Abacus 3.1, Pharmacy Calculator Product Usage: Provide pharmacy calculations for automated compounding.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1929-2014·2014-07-02
Microgenics Recalls MAS Omni Immune Controls Due to Labeling Error
Microgenics Corporation is recalling MAS Omni Immune Controls because the package insert failed to reflect the removal of the constituent Inhibin A.
Product
MAS Omni Immune Controls
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1930-2014·2014-07-02
Microgenics Recalls MAS Omni Immune PRO Controls Due to Labeling Error
Microgenics Corporation is recalling MAS Omni Immune PRO Controls because the package insert failed to reflect the removal of the constituent Inhibin A.
Product
MAS Omni Immune PRO Controls
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·041-2014·2014-06-26
Raw Pork Nuggets Recalled for Undeclared Wheat Allergen
Mr. Wok Foods is recalling raw pork nuggets because they contain undeclared wheat, a known allergen.
Product
Mr Wok Foods Inc. dba Maxfield Foods — Nevada Firm Recalls Raw Pork Nugget Products Containing Wheat Due To Misbranding and Undeclared Allergens
Category
Food
Distribution
1 state
HighUSDA FSIS·039-2014·2014-06-25
K & W Sausage Recalls Products for Undeclared Soy and Wheat Allergens
K & W Sausage is recalling specific sausage products because they contain undeclared soy and wheat, which are known allergens.
Product
K & W Sausage — Iowa Firm Recalls Sausage Products Containing Soy and Wheat Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-1833-2014·2014-06-25
Synthes External Fixation Systems Recalled for MR Labeling Changes
Synthes, Inc. is recalling external fixation systems because labeling changes were made to reflect updated protocols for Magnetic Resonance (MR) imaging safety designations.
Product
Synthes External Fixation Systems (Small, Medium, Large and DO), bone fixation appliance components.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1805-2014·2014-06-25
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products FS Calibrator 1
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products FS Calibrator 1 because calibrator values were assigned using a reference method that was not fully validated.
Product
VITROS (R) Chemistry Products FS Calibrator 1, Product Code/ Catalog Number 6801873 -- For in vitro diagnostic use only --- VITROS Chemistry Products FS Calibrator 1 is used in conjunction with VITROS Chemistry Products Calibrator Kits to calibrate the VITROS 5,1 FS and 4600 Chem
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1804-2014·2014-06-25
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products Calibrator Kit 17
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 17 because calibrator values were assigned using a reference method that was not fully validated.
Product
VITROS (R) Chemistry Products Calibrator Kit 17, Product Code/ Catalog Number 6801701 -- For in vitro diagnostic use only --- VITROS Chemistry Products Calibrator Kit 17 is used in conjunction with VITROS Chemistry Products FS Calibrator 1 to calibrate VITROS 5,1 FS Chemistry Sys
Category
Medical Device
Distribution
Distributed nationwide
ModerateUSDA FSIS·040-2014·2014-06-25
Rudolph Foods Recalls Pork Cracklins Due to Undeclared MSG
Rudolph Foods is recalling 34 pounds of pork cracklins because the product contains monosodium glutamate (MSG), which is not declared on the label.
Product
Rudolph Foods Company — Recall Notification Report 040-2014 (Pork Products)
Category
Food
Distribution
6 states
ModerateFDA (Drugs)·D-1383-2014·2014-06-25
Thorne Research Recalls Captomer Capsules Marketed Without FDA Approval
Thorne Research is recalling Captomer capsules because they are marketed as dietary supplements but contain DMSA, an active drug ingredient, making them unapproved new drugs.
Product
Captomer [succinic acid (from 100 mg DMSA)] capsules, 65 mg, 45-count bottles, Manufactured By: Thorne Research, Inc., P.O. Box 25, Dover, Idaho 83825, UPC 6 93749 74002 5
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1793-2014·2014-06-25
Gen-Probe Recalls APTIMA Urine Collection Kits Due to Labeling Error
Gen-Probe Inc is recalling APTIMA Urine Collection Kits because inner pouches are mislabeled as swab collection kits.
Product
APTIMA Urine Collection Kit; Catalog Number 301040, Lots 27231, 27232, 27233, and 27234. Product Usage: The APTIMA Urine Specimen Collection Kit for Male and Female Urine Specimens is for use with APTIMA assays. The APTIMA Urine Specimen Collection Kit is intended to be used
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·037-2014·2014-06-19
Dearborn Sausage Recalls Slab Bacon for Undeclared Soy Allergen
Dearborn Sausage Company is recalling approximately 3,660 pounds of slab bacon because the product contains hydrolyzed soy protein, a known allergen, that is not declared on the label.
Product
Dearborn Sausage Company Inc — Michigan Firm Recalls Bacon Product Due To Misbranding and Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1362-2014·2014-06-18
Pharmakon Recalls Midazolam Syringes Containing Twice Stated Dosage
Pharmakon Pharmaceuticals is recalling specific lots of Midazolam syringes because they contain twice the stated amount of the drug.
Product
Midazolam 0.2 mg/2 mL 0.9% Sodium Chloride syringes, Total dosage: 0.4 mg per 2 mL, Rx Only, Pharmakon Pharmaceuticals, Inc., 14450 Getz Rd, Noblesville, Indiana, NDC 45183-0014-69.
Category
Drug
Distribution
1 state
SevereFDA (Food)·F-2020-2014·2014-06-18
T.H. Seafood Recalls Raw Frozen Black Cod Due to Labeling Error
T.H. Seafood Inc. is recalling raw, frozen black cod because the packaging lacks instructions to keep the product frozen or refrigerated after thawing.
Product
Raw, frozen, vacuum-packaged black cod (portions, fillets, and whole fish, various sizes).
Category
Food
Distribution
1 state
SevereFDA (Food)·F-2022-2014·2014-06-18
T.H. Seafood Recalls Raw Frozen Salmon Due to Labeling Defect
T.H. Seafood Inc. is recalling raw, frozen, vacuum-packaged salmon because the labeling failed to instruct consumers to keep the product frozen or thawed under refrigeration to control Clostridium botulinum.
Product
Raw, frozen, vacuum-packaged salmon (portions, fillets, and whole fish, various sizes).
Category
Food
Distribution
1 state
SevereFDA (Food)·F-2019-2014·2014-06-18
T.H. Seafood Recalls Frozen Rockfish Due to Missing Labeling Instructions
T.H. Seafood Inc. is recalling approximately 2,000 lbs of raw, frozen rockfish because packaging labels failed to instruct consumers to keep thawed fish under refrigeration to control Clostridium botulinum.
Product
Raw, frozen, vacuum-packaged rock fish (portions, fillets, and whole fish, various sizes).
Category
Food
Distribution
1 state
HighFDA (Food)·F-2013-2014·2014-06-18
United Bakery Recalls Parmesan Bread Sticks Due to Undeclared Egg Allergen
United Bakery is recalling Parmesan Bread Sticks because egg is an ingredient in the cheese but is not declared on the label.
Product
United Bakery Grissini Parmesan Bread Sticks,; Made with Extra Virgin Olive Oil and Grano Padano Cheese; All Natural, Trans Fat Free; Packaged in 8 oz (227g) and 4.5 oz (128g) containers. Also packaged for Safeway - Safeway Select Parmesan Grissini Breadsticks, 8 oz. (227g)
Category
Food
Distribution
5 states
HighFDA (Food)·F-2018-2014·2014-06-18
Poco Pac Salad Dressing Recalled for Undeclared Egg Allergen
Diamond Crystal Brands is recalling Poco Pac Salad Dressing packets because they contain egg, which is not listed on the label.
Product
Poco Pac Salad Dressing, Distributed by Diamond Crystal Brands, Inc., Savannah, GA 31405, and packaged in single serve packets of 9 or 12 grams (g) of product. Product is packed as follows: 500 ct-9g (Product Code: 86251), 200ct-9g (Product Code: 86242) and 200 ct-12g (Product Co
Category
Food
Distribution
19 states
HighFDA (Food)·F-2021-2014·2014-06-18
T.H. Seafood Recalls Frozen Halibut Due to Missing Refrigeration Labeling
T.H. Seafood Inc. is recalling raw, frozen halibut because the packaging lacks instructions to keep thawed fish under refrigeration, posing a Clostridium botulinum risk.
Product
Raw, frozen, vacuum-packaged halibut (portions, fillets, and whole fish of various sizes).
Category
Food
Distribution
1 state
HighFDA (Drugs)·D-1363-2014·2014-06-18
Pantoprazole Sodium Tablets Recalled Due to Potential Mispackaging with Lorazepam
Legacy Pharmaceutical Packaging is recalling Pantoprazole Sodium tablets because some cartons may contain Lorazepam tablets instead.
Product
Pantoprazole Sodium, Delayed-release tablets, USP, 40 mg tablets, 100 (10x10) unit dose packages, Manufactured by Dr. Reddy's Laboratories Limited, India and Distributed by Major Pharmaceuticals, Livonia, MI --- NDC 0904-6235-61
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-2014-2014·2014-06-18
La Terra Fina Spinach and Kale Dip Recalled for Labeling Error
La Terra Fina Inc. is recalling specific lots of Spinach & Kale Dip and Spread because one lot's ingredient statement incorrectly lists ingredients for spinach dip.
Product
La Terra Fina All Natural Spinach & Kale Dip and Spread; Made with Greek Yogurt; Net Wt. 10 oz. (.625 lb) 284 g UPC 6 40410 51350 1; La Terra Fina, Union City, CA.
Category
Food
Distribution
3 states