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.

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.

2576–2600 of 9607

ModerateFDA (Devices)·Z-2448-2019·2019-09-11
LeMaitre Aortic Occlusion Catheter Recalled for Incorrect Size Labeling
LeMaitre Vascular is recalling 62 units of Aortic Occlusion Catheters because the packaging lists the incorrect device size.
Product
The LeMaitre Aortic Occlusion Catheter is a single lumen catheter with a latex balloon, it is offered in two balloon sizes: 28 mm or 45mm. The single lumen acts as the inflation lumen for the balloon and is indicated by the white stopcock. Other features include a balloon wall th
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2437-2019·2019-09-11
Heidelberg SPECTRALIS Ophthalmic Imaging Device Recalled for Data Display Error
Heidelberg Engineering is recalling 29 SPECTRALIS ophthalmic imaging devices because a software configuration error may cause incorrect display of patient master data.
Product
SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic diagnostic imaging device.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2105-2019·2019-09-11
Vitony Bakery Cheese-Guava Pudding Cake Recalled for Undeclared Dyes
Vitony Bakery is recalling 2,354 units of Cheese-Guava Pudding Cake because the product fails to declare FD&C Yellow #5 and FD&C Yellow #6.
Product
Vitony Bakery, Bizcocho de Queso y Guayaba (Cheese-Guava Pudding Cake); Peso Neto 14 ONZ. (397 G)
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-2095-2019·2019-09-11
Lipton Diet Iced Peach Tea Recalled for Undeclared Ingredients
Pepsi Bottling Ventures is recalling Lipton Diet Iced Peach Tea bottles due to undeclared Malic Acid and Citrus Pectin.
Product
Lipton DIET ICED TEA PEACH 6/16.9 oz plastic bottles MANUFACTURED BY INDEPENDENT PRODUCERS FOR THE PEPSI/LIPTON TEA PARTNERSHIP, PURCHASE, NY 10577
Category
Food
Distribution
1 state
LowFDA (Devices)·Z-2433-2019·2019-09-11
Getinge CO2 Absorber Recalled for Reversed Expiration and Manufacturing Dates
Getinge is recalling 1,444 boxes of disposable CO2 absorbers because the expiration and manufacturing dates on the labels are reversed.
Product
Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2444-2019·2019-09-11
AngioDynamics VenaCure EVLT NeverTouch Procedure Kit Recalled for RFID Error
AngioDynamics is recalling VenaCure EVLT NeverTouch Procedure Kits because an RFID programming error prevents the product from being used with the laser source.
Product
AngioDynamics VenaCure EVLT NeverTouch Procedure Kit, 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG, Catalog Number 11403012
Category
Medical Device
Distribution
8 states
HighFDA (Food)·F-2120-2019·2019-09-04
Olive Bakery Recalls Red Bean and Walnut Bread for Allergen Mislabeling
Olive Bakery is recalling three packages of red bean and walnut bread sold in Oregon and Washington due to undeclared wheat and walnut allergens.
Product
Red/ Walnut bread packages contain two bread pastries filled with red bean paste filling coated with egg on the outside and topped with walnuts. They are packaged together in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included o
Category
Food
Distribution
2 states
HighFDA (Food)·F-2116-2019·2019-09-04
Olive Bakery Cream Horns Recalled for Undeclared Wheat and Soy Allergens
Olive Bakery is recalling Cream Horns because the label fails to declare wheat and soy lecithin, posing a risk to consumers with allergies.
Product
Cream Horns packages contain one bread pastry filled with non-dairy whipped cream filling. Product is packaged in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included on the label. The packaging contains white printing label
Category
Food
Distribution
2 states
HighFDA (Food)·F-2112-2019·2019-09-04
Olive Bakery Peanut Crunch Bread Recalled for Wheat Labeling Error
Olive Bakery is recalling five packages of Peanut Crunch bread because the label declares flour but fails to declare wheat, a major allergen.
Product
Peanut Crunch bread packages contain two bread pastries with no filling and topped with a peanut butter crunch on the outside. They are packaged together in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included on the label. Th
Category
Food
Distribution
2 states
HighFDA (Food)·F-2109-2019·2019-09-04
Olive Bakery Red Bean Bread Recalled for Wheat Mislabeling
Olive Bakery is recalling 41 packages of Red Bean Bread because the label lists flour but fails to declare wheat, a major allergen.
Product
Red Bean bread package contains two bread pastries filled with red bean paste filling, packaged in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included on the label. The packaging contains white printing label and reads in part
Category
Food
Distribution
2 states
HighFDA (Food)·F-2111-2019·2019-09-04
Olive Bakery Recalls White Bean Bread for Wheat Allergen Mislabeling
Olive Bakery is recalling White Bean bread because the label lists flour but fails to declare wheat, a major allergen. The product was distributed in Oregon and Washington.
Product
White Bean bread is filled with white bean paste filling and topped with black sesame seeds, two pieces are packaged together in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included on the label. The packaging contains white pr
Category
Food
Distribution
2 states
HighFDA (Food)·F-2118-2019·2019-09-04
Olive Bakery Chestnut Bread Recalled for Undeclared Wheat Allergen
Olive Bakery is recalling chestnut bread packages because the label declares flour but fails to declare wheat, a major food allergen.
Product
Chestnut bread packages contain two bread pastries filled with white bean paste filling and topped with sesame seeds on the outside. Product does NOT contain any chestnut. They are packaged together in a clear plastic bag with a fold down stick seal. No net weight or nutritiona
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-2364-2019·2019-09-04
CooperSurgical Recalls TransWarmer Infant Mattresses Due to Burn Risk
CooperSurgical is recalling TransWarmer Warming Infant Transport Mattresses because some units lack updated instructions prohibiting use with other heat devices, which could cause skin burns.
Product
TransWarmer Warming Infant Transport Mattress, Model no. 20421 Product Usage: The TransWarmer¿ Warming Infant Transport Mattress is gel-filled, disposable mattress that provides heat for up to two hours when cold stress is a concern. The patented WarmGel heats up to 104 (whe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2113-2019·2019-09-04
Olive Bakery Cream Bread Recalled for Allergen Mislabeling
Olive Bakery is recalling cream bread packages because the label fails to declare wheat and soy lecithin, posing a risk to consumers with allergies.
Product
Cream bread packages contain two bread pastries filled with custard filling. They are packaged together in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included on the label. The packaging contains white printing label and read
Category
Food
Distribution
2 states
HighFDA (Food)·F-2117-2019·2019-09-04
Olive Bakery Peanut Butter Bread Recalled for Allergen Mislabeling
Olive Bakery is recalling Peanut Butter Bread packages because the label fails to declare wheat and soy lecithin. The product was distributed in Oregon and Washington.
Product
Peanut Butter bread packages contain two bread pastries filled with peanut butter filling. They are packaged together in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included on the label. The packaging contains white printing l
Category
Food
Distribution
2 states
HighFDA (Food)·F-2110-2019·2019-09-04
Olive Bakery Green Bean Bread Recalled for Undeclared Wheat Allergen
Olive Bakery is recalling Green Bean bread because the label lists flour but fails to declare wheat, a major allergen.
Product
Green Bean bread topped with black sesame seeds, packaged together in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included on the label. The packaging contains white printing label and reads in part: ***Olive bakery ***Ingredie
Category
Food
Distribution
2 states
HighFDA (Food)·F-2119-2019·2019-09-04
Olive Bakery Sweet Potato Bread Recalled for Wheat Mislabeling
Olive Bakery is recalling three packages of Sweet Potato Bread because the label lists flour but fails to declare wheat, a major allergen.
Product
Sweet Potato bread packages contain two bread pastries filled with white bean paste filling topped with black sesame seeds and cinnamon. They are packaged together in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included on the la
Category
Food
Distribution
2 states
HighFDA (Food)·F-2115-2019·2019-09-04
Olive Bakery Recalls Bavarian Bread Packages for Allergen Mislabeling
Olive Bakery is recalling three packages of Bavarian bread pastries because the label fails to declare wheat and soy lecithin.
Product
Bavarian bread packages contain two bread pastries filled with Bavarian cream filling. They are packaged together in a clear plastic bag with a fold down stick seal. No net weight or nutritional information is included on the label. The packaging contains white printing lab
Category
Food
Distribution
2 states
ModerateFDA (Devices)·Z-2360-2019·2019-09-04
Leventon DOSI-FUSER Infusion Pumps Recalled for Lack of FDA Clearance
Leventon S. A. U. is recalling DOSI-FUSER infusion pumps because they lack FDA 510(k) clearance, making them misbranded.
Product
DOSI-FUSER 12591 5-500D1 -USA, 12591 5-600D1 -USA Provide parenteral drug infusions at a constant flow without impeding patient mobility
Category
Medical Device
Distribution
6 states
ModerateFDA (Drugs)·D-1846-2019·2019-09-04
Alkermes Recalls Vivitrol Kits Due to Incorrect Needle Packaging
Alkermes is recalling 6,514 Vivitrol kits because 1-inch needles were incorrectly placed in sleeves labeled for 1.5-inch needles. The drug vials are not impacted.
Product
VIVITROL — VIVITROL (NALTREXONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2408-2019·2019-09-04
Ad-Tech Skull Anchor Bolts Recalled for Incorrect MRI Approval Labeling
Ad-Tech Medical Instrument Corporation is recalling Skull Anchor Bolts because supplemental information incorrectly indicated they were approved for use in the MR environment.
Product
Skull Anchor Bolts
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2432-2019·2019-09-04
Baxter Recalls Exactamed Oral Dispensers Due to Mixed Sizes
Baxter Healthcare is recalling Exactamed 5 mL Oral Dispensers because pharmacy packs may contain 10 mL dispensers.
Product
EXACTAMED Oral Dispensers, 5mL, AMBER: PHARMACY PACK, REF H9388505, x500 PHARMACY PACK, REF H9388105, x100 COST CONTAINMENT, REF H93884205, x1500
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2406-2019·2019-09-04
Ad-Tech Medical Recalls Subdural Electrodes Due to Incorrect MR Safety Labeling
Ad-Tech Medical Instrument Corporation is recalling subdural electrodes because supplemental information incorrectly stated they were approved for use in MRI environments.
Product
Dual-Sided Interhemispheric, Grid, Intraoperative, Strip, Wyler Subdural Electrodes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2407-2019·2019-09-04
Ad-Tech Medical Recalls Depth Electrodes Due to Incorrect MR Safety Labeling
Ad-Tech Medical Instrument Corporation is recalling depth electrodes because supplemental information incorrectly stated they were approved for use in the MR environment.
Product
Depth Electrodes, Foramen Ovale Depth Electrodes, Macro Micro Depth Electrodes, Spencer Probe Depth Electrodes, Wyler Sphenoidal Depth Electrodes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2396-2019·2019-09-04
Ad-Tech Spencer Probe Depth Electrodes Recalled for Incorrect Contact Count Labeling
Ad-Tech Medical Instrument Corporation is recalling 18 Spencer Probe Depth Electrodes because two units labeled as 8-contact were actually 6-contact. No patient impact was reported.
Product
AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth Electrodes (Depth Electrodes, Foramen Ovale Depth Electrodes, Macro Micro Depth Electrodes, Spencer Probe Depth Electrodes, Wyler Sphenoidal Depth Electrodes) are intended for temporary (< 30 days) use wit
Category
Medical Device
Distribution
Distributed nationwide