Hazard

Mislabeling recalls

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

What the numbers show

Total: 395
Critical: 20
Severe: 45
Most recent: 2026-07-22

Of the 395 mislabeling recalls we have scored against our rubric, 20 (5%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 45 (11%) 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 mislabeling 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.

301–325 of 395

HighFDA (Food)·F-0335-2023·2023-02-08
Ube Ensaymada recalled for undeclared wheat allergen
Joy Joys Bakery LLC is recalling Ube Ensaymada sold in Washington and Oregon due to undeclared wheat. The product label lists flour but does not specify wheat flour.
Product
Ube Ensaymada, UPC 6658266481. Product is packaged in plastic clear clamshell container and there are 4 pieces per container. Ingredients: Cream Cheese, Cheese, Butter, Milk, Sugar, Salt, Water, Yeast, Flour, Egg. Joy Joy s Bakery contact information: (253) 507-5259, 11107 Pacifi
Category
Food
Distribution
2 states
HighFDA (Food)·F-0292-2023·2023-01-25
Melissa's Pasta Para Duris Recalled for Undeclared Wheat Allergen
Melissa's Pasta Para Duris is being recalled for containing wheat that is not declared on the label. Anyone with a wheat allergy should discard the product or return it to their retailer.
Product
Pasta Para Duris 12 oz. (340g) Brand Name: Melissa's UPC: 045255 152739 Distributed by: World Variety Produce, Inc. PO Box 514599 LA, CA 90051 Clear plastic bag with front label Package size: 6 count
Category
Food
Distribution
6 states
HighFDA (Food)·F-0206-2023·2022-12-28
Red Button French Silk Pies Recalled for Undeclared Almonds
Rocky Mountain Pies is recalling Red Button Vintage Creamery French Silk Pies because some contain Turtle Cream Pies with almonds not declared on the label. Consumers with almond allergies are at risk.
Product
Red Button Vintage Creamery French Silk Pie, Net Wt. 31.88 oz. (904g), in a clear plastic dome and black plastic base, UPC 0 41172 81290 9, Distributed By: Associated Food Stores, Salt Lake City, Utah 84119 RMYA0421" printed on sleeve. Keep refrigerated.
Category
Food
Distribution
9 states
ModerateFDA (Devices)·Z-0725-2023·2022-12-28
Intradental periodontal picks recalled for mislabeling by Young Dental
Young Dental Manufacturing has recalled Denticator PICK-A-DENT intradental picks due to mislabeling. The recall affects 600 packs distributed in Iowa, New York, Pennsylvania, Tennessee, Texas, and Canada.
Product
Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0169-2023·2022-11-30
Tiramisu Twist Cookies recalled for undeclared tree nuts
DAISO CALIFORNIA WAREHOUSE is recalling Tiramisu Twist Cookie 3.4 oz. packages due to undeclared tree nuts. Consumers with tree nut allergies face allergic reaction risk if they consume this product unknowingly.
Product
Tiramisu Twist Cookie 3.4 oz. packaged in a gold bag with a large image of two cookies on the package. SKU 4562138450820 3.4 oz. packages, 12 units per case Product of Malaysia
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-0266-2023·2022-11-30
Allison Medical recalls InControl insulin syringes for incorrect needle gauge labeling
Allison Medical is recalling 150,000 InControl insulin syringes distributed in Texas due to incorrect package labeling of needle gauge. The mislabeled packages may lead patients to unknowingly select the wrong needle size.
Product
InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Category
Medical Device
Distribution
1 state
SevereFDA (Food)·F-0152-2023·2022-11-23
Zingerman's Paw Paw Gelato recalled for undeclared egg allergen
Zingerman's Creamery is recalling Paw Paw Gelato in pint (16 oz) and quart (32 oz) sizes due to undeclared egg. Consumers with egg allergies should not consume this product.
Product
Zingerman's Paw Paw Gelato pint (16oz) and quart (32oz) sizes
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-0233-2023·2022-11-23
GentleWave System APM Procedure Instruments recalled for erroneous carton labels
Sonendo Inc is recalling 15 GentleWave System APM Procedure Instruments (Model GW-APM-PI02) due to erroneous unit carton labels. The instruments were distributed worldwide, including Ohio and Canada.
Product
GentleWave System APM Procedure Instrument with Matrix REF GW-APM-PI02
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0138-2023·2022-11-16
Vegan Golden Nuggets recalled for undeclared egg allergen
DA CHENG VEGETARIAN FOOD INC. recalls Vegan Golden Nuggets for containing undeclared egg. The product was distributed to restaurants and retail stores in Utah, Virginia, Texas, and California.
Product
Vegan Golden Nuggets, (6.6 lb bags) Ingredients: (NON GMO) Textured Soybean Fiber, Isolated Soy Protein, Soybean Oil, Sugar, Salt, Pepper, Vegan Chicken Flavor Seasoning (Food Additive: Modified Starch Seasoning, Yeast Extract (Yeast Extract, Salt, Water), Crisp Powder, Bread Pow
Category
Food
Distribution
4 states
HighFDA (Food)·F-0102-2023·2022-11-09
Bella Cucina Sweet Pepper Pesto recalled due to undeclared milk allergen
Bella Cucina Artful Food Sweet Pepper Pesto is being recalled because the label does not declare milk as an ingredient. Consumers with milk allergies could experience a serious allergic reaction.
Product
Bella Cucina Artful Food Sweet Pepper Pesto Net Wt. 3 oz (84.5g) jar, UPC 6 19193 00233 5 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
ModerateFDA (Devices)·Z-0120-2023·2022-11-02
Medline Blood Culture Collection Kits Recalled for Incorrect Expiration Dates
Medline recalls Adult Blood Culture Collection Kits due to incorrect expiration dates on kit components. The expiration dates on the CHG Solution and Bactec bottle plastic do not match the dates listed on the kit packaging.
Product
MEDLINE ADLT BLOOD CLUTURE COLLECT KIT, Reorder #: DYNDH1245
Category
Medical Device
Distribution
Distributed nationwide
SevereUSDA FSIS·037-2022·2022-10-26
New Universal Nourishment Recalls Beef Burger Patties Produced Without Inspection
New Universal Nourishment LLC is recalling approximately 368 pounds of raw, frozen beef burger patties that were repackaged and distributed without federal inspection.
Product
New Universal Nourishment LLC Recalls Beef Burger Patty Products Produced Without Benefit of Inspection
Category
Food
Distribution
1 state
HighFDA (Food)·F-0069-2023·2022-10-26
Tastykake Glazed Cherry Pie Recalled Due to Undeclared Soy Lecithin
Flowers Foods is recalling Tastykake Glazed Cherry Pie due to undeclared soy lecithin in the product. The recalled product may pose a health risk to consumers with soy allergies.
Product
TASTYKAKE GLAZED CHERRY PIE NET WT 4.5 OZ (128g) UPC 0 25600 00969 7 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
Category
Food
Distribution
50 states
HighFDA (Food)·F-0050-2023·2022-10-26
Karlsburger Kitchens Turkey Gravy Mix Contains Undeclared Gluten
Karlsburger Kitchens NSLP 140 Turkey Gravy Mix labeled as gluten-free contains undeclared gluten. The product was distributed in Kansas, Minnesota, Nebraska, and Wisconsin.
Product
Karlsburger Kitchens NSLP 140 Turkey Gravy Mix, Gluten Free. Packaged in the following sizes: 1. Item 32713. Net Weight 13 oz. (368 gm). 2. Item 32725. Net Weight 25 lb. (11.34 kg). Manufactured in a plant that handles Gluten. Karlsburger Foods, Inc., Monticello, MN
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-0023-2023·2022-10-19
Hobbs Posi-Stop Injection Needle recalled for incorrect expiration date on label
Hobbs Medical is recalling Posi-Stop Injection Needles (lot numbers ending in R) due to incorrect expiration dates on labels that extend shelf life. Affected devices were distributed in the US from March 2018 to September 2020.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4718
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0016-2023·2022-10-19
Hobbs Medical Polypectomy Snare Recalled for Incorrect Expiration Date
Hobbs Medical is recalling Polypectomy Snare devices (Catalog Number 4564) due to incorrect expiration dates on labels that extend the stated shelf life. The 35 affected units, distributed in the US and select countries, may be used beyond their actual safe shelf life.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4564
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0059-2023·2022-10-19
Freeman Pancreatic Flexi-Stent labeled with incorrect expiration dates
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stents with incorrect expiration dates on device labels that extend shelf life. Devices were distributed in the US and internationally from March 2018 to September 2020.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6548
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0034-2023·2022-10-19
Hobbs Medical Grasping Forceps Recalled for Incorrect Expiration Date Labeling
Hobbs Medical, Inc. is recalling Grasping Forceps due to incorrect expiration dates on device labels. Affected devices may be used beyond their safe shelf life if the mislabeled expiration dates are not corrected.
Product
Hobbs Medical Grasping Forceps Catalog Number:5004
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0031-2023·2022-10-19
Hobbs Helical Retrieval Basket recalled for incorrect expiration date
Hobbs Medical recalled 10 units of its Helical Retrieval Basket due to mislabeled expiration dates that extend the product's shelf life, affecting devices distributed in the US and select countries between 2018 and 2020.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4824
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0029-2023·2022-10-19
Hobbs Helical Retrieval Basket Recall: Incorrect Device Label Expiration Date
Hobbs Medical is recalling Helical Retrieval Baskets due to incorrect expiration dates on device labels. The mislabeling extends the shelf life, potentially allowing use of expired devices.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4816
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0048-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit recalled for mislabeled expiration dates
Hobbs Medical is recalling the Freeman Pancreatic Flexi-Stent Kit because the device label displays an incorrect expiration date that extends the shelf life. U.S. distribution of affected devices occurred between March 25, 2018 and September 28, 2020.
Product
Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6352
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1858-2022·2022-10-12
Hologic BioZorb LP Implant Markers Recalled Due to Mislabeled Expiration Date
Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.
Product
The BioZorb LP Marker is an implantable radiopaque marker used to facilitate visualization of a soft tissue site. The BioZorb LP Marker is comprised of a bioabsorbable PLA (polylactic acid) component which resorbs completely in 1 year or more and a permanent component (titanium).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0005-2023·2022-10-12
Wright Medical EVOLVE Proline Stem Labeling Error Recall
Wright Medical is recalling EVOLVE Proline Stem devices due to labeling errors where the outer package does not match the device inside. Affected devices are size-mismatched, which could lead to incorrect surgical placement.
Product
stryker EVOLVE, Proline Stem, CoCr, Size: +2, O: 705mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radial head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1539-2022·2022-09-21
Teva Amphetamine Tablets Recalled Due To Incorrect Strength Labeling
Teva Pharmaceuticals is recalling 83,703 bottles of prescription amphetamine tablets nationwide because bottles labeled as 15 mg strength actually contain 20 mg tablets, creating risk of unintended overdose. Patients should contact their pharmacy or healthcare provider.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1734-2022·2022-09-21
GNC Vitamin B-6 supplement mislabeled; bottles contain Pycnogenol instead
GNC Vitamin B-6 100mg dietary supplement bottles actually contain Pycnogenol due to a filling line error. The product was distributed across all 50 US states and multiple international locations.
Product
GNC Vitamin B-6 100mg 100 VEGETARIAN TABLETS DIETARY SUPPLEMENTS Distributed by: General Nutrition Corporation Pittsburgh, PA 15222 UPC 0 48107 20584 3
Category
Food
Distribution
0 states