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.

7026–7050 of 9611

ModerateFDA (Devices)·Z-2724-2014·2014-10-08
Instrumed Recalls Reusable Laparoscopic Instruments for Updated Safety Instructions
Instrumed International is recalling 3,093 reusable laparoscopic instruments to add caution statements regarding voltage limits and useful life to the Instructions For Use.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for manip
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2730-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Warnings
Instrumed International is recalling reusable laparoscopic instruments to add caution statements regarding voltage limits and product useful life.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for manip
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2725-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions
Instrumed International is recalling 83 reusable laparoscopic instruments to add caution statements regarding voltage limits and product useful life.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for manip
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2727-2014·2014-10-08
Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions
Instrumed International is recalling 895 reusable laparoscopic instruments to add caution statements regarding voltage limits and product life to the Instructions For Use.
Product
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for manip
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1606-2014·2014-10-01
Baxter Recalls Potassium Chloride Bags Due to Mispackaging Error
Baxter Healthcare is recalling 148,632 bags of Potassium Chloride Injection because shipping cartons were incorrectly labeled and contained Gentamicin Sulfate Injection instead.
Product
POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-2496-2014·2014-10-01
Roots Hot Chipotle Hummus Recalled for Missing Soy Allergen Labeling
Roots Organic Gourmet is recalling Hot Chipotle Hummus because the label lists Tamari but fails to state 'Contains Soy.'
Product
Roots, Hot Chipotle Hummus, Net Wt. 8oz (227 g), and 16 oz. (454 g), Gluten-Free Vegan, UPC: 860971000054, and 723175787612, 166 W. Haywood St., Asheville, NC 2801, RootsFood.com. This product is packaged in 8 oz. and 16 oz. non-flexible plastic tubs.
Category
Food
Distribution
6 states
HighFDA (Food)·F-2492-2014·2014-10-01
Roots Organic Gourmet Recalls Original Hummus Due to Missing Soy Labeling
Roots Organic Gourmet is recalling Original Hummus because the label fails to state 'Contains Soy' despite listing Tamari as an ingredient.
Product
Roots, Original Hummus, Net Wt. 8oz (227 g), and 16oz (454 g), Gluten-Free Vegan, UPC: 860971000009, and 723175787629, 166 W. Haywood St., Asheville, NC 2801, RootsFood.com. This product is packaged in 8 oz. and 16 oz. non-flexible plastic tubs.
Category
Food
Distribution
6 states
HighFDA (Food)·F-2499-2014·2014-10-01
Roots Lima Bean Hummus Recalled for Missing Soy Allergen Labeling
Roots Organic Gourmet is recalling Lima Bean Hummus because the label lists Tamari but fails to state 'Contains Soy.'
Product
Roots, Lima Bean Hummus, Net Wt. 8 oz (227 g), Gluten-Free Vegan, UPC: 723175787599, 166 W. Haywood St., Asheville, NC 2801, RootsFood.com.This product is packaged in 8 oz. non-flexible plastic tubs.
Category
Food
Distribution
6 states
HighFDA (Food)·F-2497-2014·2014-10-01
Roots Black Bean Hummus Recalled for Missing Soy Allergen Labeling
Roots Organic Gourmet is recalling Black Bean Hummus because the label lists Tamari but lacks a 'Contains Soy' statement.
Product
Roots, Black Bean Hummus, Net Wt. 8oz (227 g), and 16 oz. (454 g), Gluten-Free Vegan, UPC: 860971000030, and 723175787636, 166 W. Haywood St., Asheville, NC 2801, RootsFood.com. This product is packaged in 8 oz. and 16 oz. non-flexible plastic tubs.
Category
Food
Distribution
6 states
HighFDA (Food)·F-2498-2014·2014-10-01
Roots Spinach Hummus Recalled for Missing Soy Allergen Labeling
Roots Organic Gourmet is recalling Spinach Hummus because the label lists Tamari but lacks a 'Contains Soy' statement.
Product
Roots, Spinach Hummus, Net Wt. 8 oz (227 g), Gluten-Free Vegan, UPC: 860971000047, 166 W. Haywood St., Asheville, NC 2801, RootsFood.com. This product is packaged in 8 oz. non-flexible plastic tubs.
Category
Food
Distribution
6 states
HighFDA (Food)·F-2495-2014·2014-10-01
Roots Roasted Red Bell Pepper Hummus Recalled for Missing Soy Labeling
Roots Organic Gourmet is recalling Roasted Red Bell Pepper Hummus because the label fails to state 'Contains Soy' despite listing Tamari as an ingredient.
Product
Roots, Roasted Red Bell Pepper Hummus, Net Wt. 8oz (227 g), and 16oz. (454 g), Gluten-Free Vegan, UPC: 860971000023, and 723175787605, 166 W. Haywood St., Asheville, NC 2801, RootsFood.com. This product is packaged in 8 oz. and 16 oz. non-flexible plastic tubs.
Category
Food
Distribution
6 states
HighFDA (Food)·F-2494-2014·2014-10-01
Roots Thai Coconut Curry Hummus Recalled for Missing Soy Allergen Labeling
Roots Organic Gourmet is recalling Thai Coconut Curry Hummus because the label lists Tamari but lacks a 'Contains Soy' statement.
Product
Roots, Thai Coconut Curry Hummus, Net Wt. 8oz (227 g), Gluten-Free Vegan, UPC: 860971000092, 166 W. Haywood St., Asheville, NC 2801, RootsFood.com. This product is packaged in 8 oz. non-flexible plastic tubs.
Category
Food
Distribution
6 states
HighFDA (Food)·F-2493-2014·2014-10-01
Roots Roasted Garlic Hummus Recalled for Missing Soy Allergen Labeling
Roots Organic Gourmet is recalling Roasted Garlic Hummus because the label lists Tamari but lacks a 'Contains Soy' statement.
Product
Roots, Roasted Garlic Hummus, Net Wt. 8oz (227 g), Gluten-Free Vegan, UPC: 860971000016, 166 W. Haywood St., Asheville, NC 2801, RootsFood.com. This product is packaged in 8 oz. non-flexible plastic tubs.
Category
Food
Distribution
6 states
HighFDA (Food)·F-2500-2014·2014-10-01
Roots Organic Gourmet Recalls Oil Free Original Hummus for Missing Soy Labeling
Roots Organic Gourmet is recalling Oil Free Original Hummus because the label lists Tamari but fails to state 'Contains Soy.'
Product
Roots, Oil Free Original Hummus, Net Wt. 8 oz (227 g), Gluten-Free Vegan, UPC: 723175787599, 166 W. Haywood St., Asheville, NC 2801, RootsFood.com.This product is packaged in 8 oz. non-flexible plastic tubs.
Category
Food
Distribution
6 states
HighFDA (Food)·F-2522-2014·2014-10-01
Southern Home Mozzarella Sticks Recalled for Wheat Allergen Mislabeling
Great American Appetizers is recalling Southern Home Mozzarella Sticks because the ingredient list includes wheat, but the 'Contains' statement omits it.
Product
Product is packaged in a cardboard box and labeled in part, "SOUTHERN HOME Mozzarella Sticks***CONTAINS: WHEY, MILK, EGG, SOY***DISTRIBUTED BY SOUTHERN HOME P.O.BOX 99 MAULDIN, SC 29662***" 6/case 30oz UPC 607880027150
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-2513-2014·2014-10-01
Frito-Lay Recalls Oven Baked Lay's BBQ Crisps Due to Packaging Error
Frito-Lay is recalling Oven Baked Lay's BBQ flavor crisps because a packaging error added a 'GF' symbol to the packages.
Product
Oven Baked Lay's BBQ flavor crisps in 1 1/8 oz package, UPC 2840007189
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2679-2014·2014-10-01
Instratek Recalls Mini Screw Sets with Faded Markings
Instratek is recalling 96 Mini Screw Sets and gauges due to faded and incorrect markings on instruments.
Product
Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Screw Set/System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2692-2014·2014-10-01
Horiba Medical Recalls ABX PENTRA Magnesium RTU Reagent for Stability Update
Horiba Medical is recalling ABX PENTRA Magnesium RTU Reagent to update on-board stability claims from 7 days to 1 day.
Product
ABX PENTRA Magnesium RTU Reagent, Part No. A11A01646 Product Usage: ABX PENTRA Magnesium RTU reagent with associated calibrators and controls are for quantitative in vitro diagnostic determination of magnesium in human serum and plasma based on a photometric test using xylidy
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2514-2014·2014-10-01
Arise & Shine Bentonite Supplement Recalled for Iron Mislabeling
Arise & Shine is recalling Hydrated Bentonite dietary supplements because the label incorrectly states 0% Daily Value of iron, while the product actually contains 106%.
Product
The product is labeled in part "***Arise & Shine Hydrated Bentonite Dietary Supplement Extra Thick Formula 32 FL OZ ***% Daily Value Iron 0***Distributed by: Arise & Shine Herbal Products 562 Parsons Drive Medford, Oregon 97501***" Product is packaged in a foil pouch with a plas
Category
Food
Distribution
0 states
CriticalFDA (Food)·F-2446-2014·2014-09-24
Dean Foods Recalls Lehigh Valley Dairy Farms Orange Juice for Undeclared Dairy
Dean Foods is recalling Lehigh Valley Dairy Farms Orange Juice from concentrate because it contains undeclared dairy. The product was distributed in several Mid-Atlantic states.
Product
Lehigh Valley Dairy Farms Orange Juice from concentrate HALF PINT (236 mL); DISTRIBUTED BY TUSCAN/LEHIGH DAIRIES, INC., A DEAN FOODS COMPANY DALLAS, TEXAS 75204 in paper cartons
Category
Food
Distribution
5 states
CriticalFDA (Drugs)·D-1589-2014·2014-09-24
American Health Packaging Recalls Mis-Labeled Ibuprofen Tablets
American Health Packaging is recalling 137,300 Ibuprofen 600 mg tablets because some cartons were mis-labeled as Oxcarbazepine 300 mg.
Product
Ibuprofen Tablets, USP, 600 mg, 100 tablets per carton (10 x 10), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, OH 43217, NDC 68084-0703-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1590-2014·2014-09-24
Oxcarbazepine Tablets Recalled Due to Labeling Error
American Health Packaging is recalling Oxcarbazepine Tablets due to a label mix-up with Ibuprofen tablets.
Product
Oxcarbazepine Tablets, 300 mg, 100 tablets per carton (10 x 10), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, OH 43217, NDC 62584-143-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-2456-2014·2014-09-24
Jenis Splendid Ice Creams Recalls Cocoa Zin Frozen Dessert for Missing Ingredients
Jenis Splendid Ice Creams LLC is recalling Cocoa Zin frozen dessert because the packaging does not list ingredients, posing a risk to consumers with allergies.
Product
Cocoa Zin- possible pints/possible half gallon. Flavor of frozen dessert on the immediate package. No ingredients listed.
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-2643-2014·2014-09-24
Siemens ADVIA Chemistry A1c_3 Calibrator Recalled for Potential Bias
Siemens is recalling ADVIA Chemistry A1c_3 Calibrators because they may cause a percent bias in HbA1c test results.
Product
ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry Systems, REF/Catalog Number/Siemens Material Number (SMN) 10491408, IVD ADVIA Chemistry A1c_3 Calibrator Information: For in vitro diagnostic use in the calibration of A1c_3 (A1c_3 and A1c_3M) and Total He
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2463-2014·2014-09-24
Jenis Splendid Ice Creams Recalls Forest Berry Sorbet for Missing Ingredient Labeling
Jenis Splendid Ice Creams LLC is recalling Forest Berry Sorbet because the frozen dessert packaging does not list ingredients, posing a risk to consumers with allergies.
Product
Forest Berry Sorbet- possible pints/possible half gallon. Flavor of frozen dessert on the immediate package. No ingredients listed.
Category
Food
Distribution
0 states