Hazard

Mis Labeling recalls

1,381 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

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.

226–250 of 1381

CriticalFDA (Devices)·Z-2035-2025·2025-07-09
Philips BiPAP V30 Auto Ventilator Recalled for Incorrect Indication Labeling
Philips Respironics recalled 5,958 BiPAP V30 Auto Ventilators worldwide due to incorrect labeling indicating use for respiratory failure patients. The device is not indicated for respiratory failure.
Product
BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0570-2025·2025-07-09
Cefazolin Injection Recalled for Incorrect Labeling as Penicillin G
Sandoz is recalling Cefazolin for Injection vials that were mislabeled as Penicillin G Potassium due to a labeling error. This mix-up poses serious medication error risks.
Product
PENICILLIN G POTASSIUM — PENICILLIN G POTASSIUM (PENICILLIN G POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2036-2025·2025-07-09
BiPAP A30 Ventilators Recalled for Improper Respiratory Failure Indication
Philips Respironics recalls BiPAP A30 and BiPAP Hybrid A30 ventilators due to labeling deficiency. The devices do not indicate for use in patients with respiratory failure.
Product
BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing more than 10 kg. BiPAP Hybrid A30 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2078-2025·2025-07-09
BD FACS Setup Beads Recall Due to Spectral Overlap Factors Table Errors
Becton Dickinson is recalling BD FACS 7-Color Setup Beads because the spectral overlap factors table contains errors that may affect flow cytometry instrument calibration and setup.
Product
REF: 335775 , BD FACS, 7-Color Setup Beads, 25 setups per kit, Rx Only, IVD. Used in flow cytometry for fluorescence compensation.
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1904-2025·2025-07-02
Broselow Pediatric Emergency Tape recalled for incorrect dosing information
SunMed's Broselow pediatric emergency tape has incorrect dosing information printed in critical zones. Using these incorrect values could cause cardiac arrest, burns, and serious electrolyte imbalances during emergency care.
Product
Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev 2 Print Version The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2010-2025·2025-07-02
Altivate Reverse shoulder implant screw package labeling mismatch FDA recall
Altivate Reverse Torx Peripheral Screw packages are labeled with incorrect size information. The included product may differ from the labeled size, posing risks if implanted in error.
Product
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 18mm Model/Catalog Number: 506-04-118 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
Category
Medical Device
Distribution
18 states
HighFDA (Devices)·Z-2011-2025·2025-07-02
Shoulder Replacement Screw Labeling Does Not Match Product Size
Encore Medical is recalling ALTIVATE REVERSE TORX PERIPHERAL SCREW surgical components because package labeling lists a different size than what is actually included. The mismatch could result in selection of an incorrectly sized component during shoulder replacement surgery.
Product
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 30mm Model/Catalog Number: 506-04-130 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
Category
Medical Device
Distribution
18 states
HighFDA (Devices)·Z-2008-2025·2025-07-02
ALTIVATE Reverse shoulder screw package labeled with incorrect size
Encore Medical is recalling ALTIVATE REVERSE TORX PERIPHERAL SCREWS due to packaging labeling errors. The label indicates one screw size, but the actual product included is a different size than stated.
Product
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number: 506-04-126 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
Category
Medical Device
Distribution
18 states
ModerateFDA (Food)·H-0088-2025·2025-07-02
Carley's Soft Baked Iced Lemon Cookies recalled for misbranded color additive
Carley's Inc. is recalling Soft Baked Iced Lemon Cookies because the label incorrectly identifies the yellow color additive as 'Artificial Yellow Color' instead of the required designation 'FD&C Yellow #5'.
Product
Carley s Soft Baked Iced Lemon Cookies, 5.34oz Plastic Tray, clear film overwrap w/ Label, 12 units per case
Category
Food
Distribution
15 states
ModerateFDA (Devices)·Z-2026-2025·2025-07-02
Jewel Precision Sterilization Container System Recalled for Instructions Mismatch
Jewel Precision Reusable Rigid Sterilization Container System (Model JP-24-6) is being recalled because the Instructions for Use do not match the FDA-cleared indications for use or sterility shelf life. Healthcare facilities should reference FDA-cleared specifications.
Product
Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog Number: JP-24-6.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0095-2025·2025-07-02
NutriLean dietary supplement recalled for undeclared food dyes
NutriLean dietary supplement capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) dyes. Approximately 94,190 capsules were distributed nationwide; consumers should stop using the product.
Product
NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0092-2025·2025-07-02
Dietary Supplement Recalled for Undeclared Red and Blue Colorants
Preventics, Inc. is recalling Super ProTHIN Plus dietary supplement nationwide because it contains undeclared Red No. 40 and Blue No. 1 colorants in its gelatin capsules (55,080 pills affected).
Product
Super ProTHIN Plus, dietary supplement. Seven Packets with 2 tablets & 4 Capsules and 1 packet with 14 Nutrilean capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1941-2025·2025-06-25
Lago X X-ray instruments recalled for incorrect safety and manufacturing labels
Spectral Instruments Inc is recalling 39 Lago X/AMI HTX X-ray instruments because the X-ray safety and manufacturing date labels do not match FDA labeling requirements.
Product
Lago X
Category
Medical Device
Distribution
0 states
HighFDA (Food)·H-0040-2025·2025-06-18
Tortilla products recalled for undeclared soy allergen
Tortilleria Xpress Inc is recalling four types of tortilla products distributed in Texas due to undeclared soy allergen. Consumers with soy allergies should not consume these products.
Product
Tortilla de mesa with 12 units per package, Tortilla Pirata with 10 units per package, Tortilla cruda especial with 20 units per package, Tortilla Cruda Pirata with 20 units per package
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1957-2025·2025-06-18
Medical Device Quality Control Kit Recall: Incorrect Microorganism Swabs Packaged
Microbiologics Inc is recalling KWIK-STICK quality control kits because affected packages contain the wrong microorganism swabs, which may delay diagnosis. Two catalog numbers (01065K and 0621K) were swapped in packaging.
Product
KWIK-STICK, Quality control kit for culture media, Catalog Numbers 01065K, Oligella urethralis derived from ATCC¿ 17960; 0621K, Staphylococcus aureus derived from NCTC 12493
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0935-2025·2025-06-18
Instant Milk Tea Brown Sugar Flavor Recalled for Undeclared Milk Allergen
R&M Refresher Instant Milk Tea Brown Sugar Flavor is recalled because it contains milk-derived ingredients (whey powder, sodium caseinate) but the label claims it is dairy-free. Consumers with milk allergies should not use this product.
Product
Instant Milk Tea Brown Sugar Flavor, R&M Refresher brand, B0D725TXQW, net wt. 1lb. Product is sold in 3-pack. Parent ASIN #B0D728CZWS 3-pack ASIN #B0D72FQVDR Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder, Sodium Caseinate***). Product of China. Dis
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0934-2025·2025-06-18
Instant Milk Tea Powder Recalled for Undeclared Milk Allergen
R&M Refresher brand Instant Milk Tea Original Flavor is recalled because it contains milk-derived ingredients but does not declare milk on the label.
Product
Instant Milk Tea Original Flavor, R&M Refresher brand, B0D71YHZX4, net wt. 1lb. Product is sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D71YHZX4 3-pack ASIN #B0D72BLQRW Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1925-2025·2025-06-18
Digital Acquisition Box devices recalled due to backwards electrode placement labels
Natus Neurology is recalling OBM00002 Digital Acquisition Box devices due to electrode placement labels applied backwards, which may cause misdiagnosis of seizure location in monitored neonates.
Product
Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box) Model/Catalog Number: OBM00002 OBM DAB (Digital Acquisition Box) Software Version: N/A Product Description: OBM00002 OBM DAB (Digital Acquisition Box) Component: N
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0823-2025·2025-06-11
Gluten-Free Bread Recalled for Undeclared Egg Allergen Due to Labeling Defect
NEW GRAINS GLUTEN FREE BAKERY is recalling Artisan Multigrain Bread due to printing quality issues that prevented clear declaration of the egg allergen on the label. Approximately 41 units were distributed in Utah.
Product
Artisan Multigrain Bread: Gluten-free multigrain bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Honey, Golden flax seed, Palm oil, Potato flour, Yeast, Sugar, Psyllium husk powder, Rice bran, Sea salt,
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0826-2025·2025-06-11
Artisan Cinnamon Raisin Bread recalled for undeclared egg allergen
New Grains Gluten Free Bakery is recalling approximately 42 units of Artisan Cinnamon Raisin Bread distributed in Utah because the label does not clearly declare egg as an allergen due to printing quality defects.
Product
Artisan Cinnamon Raisin Bread: Gluten-free cinnamon raisin bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Raisins, Honey, Tapioca flour, Golden flax seed, Palm fruit oil, Potato flour, Yeast, Sugar, Cinnamon, Psyllium
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0827-2025·2025-06-11
Gluten-Free Blueberry Bagels Recalled Due to Missing Egg Allergen Label
New Grains Gluten Free Bakery is recalling approximately 25 units of gluten-free blueberry bagels sold in Utah because the label does not clearly declare the egg allergen due to printing quality issues.
Product
Blueberry Bagels: : Gluten-free blueberry bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm fruit oil, Potato flour, Yeast, Rice bran, Psyllium husk powder, Sea salt, Xanthan gum, Enzyme. Contains: Eg
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0834-2025·2025-06-11
Gluten-Free Brownie Chocolate Chip Cookies Recalled for Undeclared Allergens
NEW GRAINS GLUTEN FREE BAKERY is recalling Brownie Chocolate Chip Cookies because labels do not clearly declare Egg, Milk, and Soy allergens due to printing quality issues. Approximately 50 units were distributed in Utah.
Product
Brownie Chocolate Chip Cookie: Gluten-free brownie chocolate chip cookies, clear plastic bag, 4 oz, 8 cookies/package Ingredients: Sugar, Eggs, Butter, Chocolate chips, White rice flour, Cocoa powder, Tapioca flour, Palm oil, Potato flour, Rice bran, Vanilla, Xanthan gum. Conta
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0835-2025·2025-06-11
New Grains Gluten Free Bakery Recalls Artisan Seasoned Croutons for Undeclared Allergens
New Grains Gluten Free Bakery is recalling Artisan Seasoned Croutons distributed in Utah because poor label printing failed to clearly declare egg and milk allergens.
Product
Artisan Seasoned Croutons: Gluten-free artisan seasoned croutons, vacuum-sealed clear plastic, 8 oz, bulk Ingredients: White rice flour, Water, Egg, Golden flax seed, Rice bran, Tapioca flour, Honey, Palm fruit oil, Potato flour, Yeast, Xanthan gum, Psyllium husk powder, Sea sa
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0828-2025·2025-06-11
Gluten-Free Cinnamon Raisin Bagels Recalled Due to Undeclared Egg Allergen
NEW GRAINS GLUTEN FREE BAKERY is recalling approximately 25 units of gluten-free cinnamon raisin bagels distributed in Utah due to undeclared egg allergen caused by label printing defects.
Product
Cinnamon Raisin Bagels: Gluten-free cinnamon raisin bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Raisins, Honey, Tapioca flour, Golden flax seed, Palm fruit oil, Potato flour, Yeast, Sugar, Cinnamon, Psyllium husk powder,
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0824-2025·2025-06-11
Gluten-free Artisan White Bread Recalled for Undeclared Egg Allergen
NEW GRAINS GLUTEN FREE BAKERY is recalling approximately 41 units of Artisan White Bread distributed in Utah due to label printing defects that fail to clearly declare the egg allergen. Consumers with egg allergies risk allergic reaction if they consume this product.
Product
Artisan White Bread: Gluten-free artisan white bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm oil, Potato flour, Yeast, Rice bran, Psyllium husk powder, Sea salt, Xanthan gum. Contains: Egg.
Category
Food
Distribution
0 states