Hazard

Mislabeling recalls

256 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 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.

101–125 of 256

HighFDA (Food)·F-0934-2024·2024-03-06
Frozen Pizza Recalled for Undeclared Milk Allergen in Plant-Based Product
Oggi Plant-Based Americana frozen pizza contains undeclared milk, posing a risk to consumers with milk allergies. The recall affects 5,040 units distributed in California, Illinois, and Washington.
Product
Oggi Pizza Plant Based Americana Beyond Meat Crumbles on Cauliflower Crust, gluten-free frozen pizza - cook before serving, net wt. 13.76oz (390g). One pizza wrapped in plastic film in a cardboard box. Retail box UPC 6 28451 68487 9. There are 12 pizza per case, and each case h
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1179-2024·2024-02-28
Biliary Endoprosthesis Labeling Mismatch Risks Incorrect Device Placement
W.L. Gore's GORE VIABIL Short Wire Biliary Endoprosthesis may be mislabeled regarding drainage holes, risking extended procedures, infections, and unplanned device removal in 24 units distributed in Georgia.
Product
GORE VIABIL Short Wire Biliary Endoprosthesis, Product labeled as (1) Catalog Number VSWVH1008, 10 mm x 8 cm; with holes; and (2) Catalog Number VSWVN1008, 10 mm x 8 cm; no holes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0855-2024·2024-02-14
Fresh noodle products recalled for undeclared wheat allergen
Alfred Louie Inc is recalling Pan Fry and Deep Fry Fresh Noodles due to undeclared wheat allergen from enriched flour sub-ingredients. 550 cases distributed in California are affected.
Product
Pan Fry Noodle Fresh Noodles, Alfred Louie, Inc. 24 Lb. cartons, Keep Refrigerated. Deep Fry Noodle Fresh Noodles, Alfred Louie, Inc. 40Lb cartons, Keep Refrigerated.
Category
Food
Distribution
1 state
HighNHTSA·22V643000·2024-02-08
2023 Forest River fifth wheels have incorrect axle rating on placard
Forest River is recalling 2023 Flagstaff and Rockwood fifth wheels because the Federal Placard lists an incorrect axle rating (5,200 lbs instead of 5,000 lbs), which could lead to vehicle overloading and increased crash risk.
Product
FOREST RIVER — 2023 FOREST RIVER FLAGSTAFF
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0816-2024·2024-02-07
Coconut Mocha snack bars recalled for undeclared soy allergen
Font Group of America Corp. is recalling ToYou Snacks Brand Coconut Mocha bars (5,670 units) distributed in the United States due to undeclared soy allergen. Consumers with soy allergies should not consume this product.
Product
Coconut Mocha, ToYou Snacks Brand, 1.41 Oz/ 40 g, packaged in kraft laminated paper, 14 bars in 1 box.
Category
Food
Distribution
0 states
ModerateFDA (Devices)·Z-0966-2024·2024-02-07
Medline Blood Culture Collection Kit Recalled for Undocumented Component Expiration
Medline is recalling blood culture collection kits because the Bactec component expiration date is not documented on the kit insert. Users who do not check the component directly risk using an expired element.
Product
MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1626B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0803-2024·2024-02-07
Solgar Glucosamine Chondroitin Recalled Due to Wrong Product Packaging Error
Nestle Health Science recalled Solgar Glucosamine Chondroitin (120-tablet bottles) distributed in six states due to a packaging error where Megasorb B-Complex was filled into mislabeled bottles.
Product
Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM, 120 Tablets per bottle. Glass Bottle, 12 per Case, Store at room temperature . Product Number -1319
Category
Drug
Distribution
6 states
SevereFDA (Food)·F-0777-2024·2024-01-31
Outrageous Oat Cookies Recalled for Undeclared Wheat Allergen
Wegmans Food Markets is recalling Outrageous Oat Cookies due to undeclared wheat. The product poses a serious health risk to consumers with wheat allergies or celiac disease.
Product
Outrageous Oat Cookies packaged in 5pk and also sold in Bulk
Category
Food
Distribution
9 states
HighFDA (Devices)·Z-0681-2024·2024-01-17
Abbott Alinity c Chemistry Analyzer Contains Unlabeled Latex Subcomponent
Abbott Laboratories is recalling 1,127 Alinity c Processing Module chemistry analyzers because unlabeled latex subcomponents are present. Users with latex allergies may experience serious allergic reactions upon contact.
Product
Alinity c Processing Module REF 03R67-01 The Alinity c Processing Module is a fully automated chemistry analyzer allowing random and continuous access, as well as priority and automated retest processing using photometric and potentiometric detection technology. The Alinit
Category
Medical Device
Distribution
47 states
HighFDA (Devices)·Z-0682-2024·2024-01-17
ARCHITECT c4000 Processing Module recalled for unlabeled latex component
Abbott ARCHITECT c4000 Processing Module laboratory analyzers are recalled due to unlabeled dry natural rubber (latex) subcomponents. Individuals with latex allergies may experience allergic reactions if exposed to the undisclosed component.
Product
ARCHITECT c4000 Processing Module REF: 02P24-01 02P24-02 02P24-40 01R24-56 01R25-56 The Abbott ARCHITECT c4000 Processing Module is designed to perform automated chemistry tests, utilizing photometry and potentiometric technology.
Category
Medical Device
Distribution
47 states
ModerateFDA (Devices)·Z-0661-2024·2024-01-17
Marketing brochure for Baxter Floseal hemostatic device contains inaccurate content
Baxter Healthcare is recalling a cardiovascular surgery marketing brochure for Baxter Floseal Hemostatic Matrix Fast Prep because it contains inaccurate content that does not match the official product instructions and prescribing information.
Product
Baxter Floseal Hemostatic Matrix Fast Prep, Product Codes: a) ADS201844, 5 mL b) ADS201845, 10mL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0639-2024·2024-01-10
Spinal fixation screws recalled due to incorrect size laser marking
Zimmer Biomet Spine Inc. is recalling Vitality Polyaxial Screws (7.5mm x 50mm) due to incorrect laser marking showing 7.5 x 40. Incorrect screw size could cause perforation and vascular damage during spinal surgery.
Product
Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0625-2024·2024-01-10
Reverse Shoulder Joint Implant System Recalled for Mislabeling
Encore Medical is recalling 17 Reverse Shoulder System e+ surgical implants (Lot 381P1167) due to mislabeling. Affected units were distributed nationwide to multiple states.
Product
Reverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2024·2023-12-20
Non-sterile Betadine solution labeled and distributed as sterile
Medline Industries is recalling 1,800 units of Sterile Betadine (Ref DYNDA1998) because the foil sachet contents are non-sterile, despite labeling that claims sterility. The recall affects units nationwide in eight states.
Product
STERILE BETADINE, REF DYNDA1998
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0487-2024·2023-12-13
Remington Medical drainage bags recalled due to packaging label date error
Remington Medical is recalling drainage bags (Lot 2325111) due to errors in the 'Use by Date' and 'Date of Manufacturer' on box labels. Approximately 3,080 units distributed in PA and FL are affected.
Product
Remington MEDICAL Drainage Bag, REF 600-D;
Category
Medical Device
Distribution
2 states
SevereFDA (Drugs)·D-0225-2024·2023-12-06
Reumo Flex caplets recalled for undeclared diclofenac content nationwide
Reumo Flex caplets packaged in 30-count boxes are being recalled because they contain undeclared diclofenac and were marketed without FDA approval. The product was distributed nationwide.
Product
Reumo Flex caplets, packaged in 30-count boxes, Manufactured by: Grupo Yepenza de Mexico, SA de CV, Comerciantes 5824 Col Arcos de Guadalupe, Zapopan Jal Mexico, UPC 7 502214 014598
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0125-2024·2023-12-06
Compounded Ophthalmic Medication Bottles Mislabeled as Single-Use Syringes
Fagron Compounding Services is recalling 756 bottles of compounded ophthalmic medication because labels incorrectly identify the container as a 0.5mL single-use syringe instead of a 5mL dropper bottle. No adverse events have been reported.
Product
Tropicamide 1% (10mg/mL), Cyclopentolate 1% (10mg/mL), Phenylephrine 2.5% (25mg/mL), Ketorolac 0.5% (5mg/mL), 5 mL bottles, For Topical Ophthalmic Use Only, Not for IV Use, This is a Compounded Drug, Hospital & Office Use Only, Fagron Sterile Services, 8710 E 34th St N Wichita, K
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0356-2024·2023-11-29
Stryker Sage PrimaFit Female Urine Management Systems recalled for undeclared latex adhesive
Sage Products is recalling approximately 174,960 Stryker Sage PrimaFit External Urine Management Systems in three lots because a small percentage may contain tape with undeclared natural rubber latex adhesive.
Product
stryker Sage PrimaFit External Urine Management System for the Female Anatomy
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0213-2024·2023-11-08
Orthopedic knee implant components mislabeled; size mix-up risk
Corin Ltd recalled 3 Unity CR Femur knee implants due to labeling errors. Size 6 implants from batch 529803 may be labeled as size 7, and vice versa.
Product
Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arthroplasty
Category
Medical Device
Distribution
3 states
ModerateFDA (Devices)·Z-0210-2024·2023-11-08
Endoscopic Vessel Harvesting System Recalled for Incorrect Outer Box Packaging
Vasoview 6 Pro endoscopic vessel harvesting systems were packaged in incorrect outer boxes displaying artwork for a different device (Vasoview Hemopro 2). The inner labels and product documentation are correct.
Product
Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2).
Category
Medical Device
Distribution
13 states
HighFDA (Food)·F-0010-2024·2023-10-18
Markside Peanut Butter Chocolate Cake Recalled for Undeclared Peanut Allergen
Fairfield Gourmet Food Corp is recalling Markside Ultimate Peanut Butter Chocolate Cake (LOT #BS23212) due to mislabeled peanut allergen. Consumers with peanut allergies should not consume the product.
Product
Markside Ultimate Peanut Butter Chocolate Cake, 7 oz.(198g), plastic package (i.e.) Clamp shell, 8 package per case, Frozen master case (keep refrigerator Retail pack. LOT # BS23212 (Manufactured on July, 31, 2023).
Category
Food
Distribution
20 states
SevereFDA (Devices)·Z-0004-2024·2023-10-11
FDA Recalls Arrow PICC Catheters with Incorrect Product Code Labels
Arrow INTERNATIONAL recalled 172 units of ErgoPack PICC catheters due to incorrect product code and product name labels. The error affected lot 13F22G0508 distributed in the US.
Product
Arrow ErgoPack Pressure Injectable Arrowg+ard Blue Advance Three-Lumen PICC pre-loaded with Arrow VPS TipTracker Stylet, REF CDC-45563-TTS; catheter, intravascular, therapeutic, long-term greater than 30 days
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0002-2024·2023-10-11
JLM Roasted Salted Pecan Halves Recalled Due to Hazelnut Substitution
Lipari Foods is recalling JLM Roasted Salted Pecan Halves because the product contains hazelnuts instead of pecans, presenting a risk to consumers with tree nut allergies.
Product
JLM Roasted Salted Pecan Halves, 10oz clear plastic container, 12 per wholesale case. Lipari number 368729, UPC 094776110049
Category
Food
Distribution
8 states
HighFDA (Food)·F-1602-2023·2023-10-04
SLR Food Dried Longans Recalled for Undeclared Sulfites
SLR Food Distribution recalled dried longans distributed in seven states because they contain undeclared sulfites. Consumers with sulfite sensitivity may experience adverse reactions.
Product
Dried Longans
Category
Food
Distribution
7 states
SevereFDA (Food)·F-1544-2023·2023-09-27
Dietary Supplement Capsules Recalled for Toxic Yellow Oleander Substitution
OBC GROUP CORP is recalling NUT DIET MAX dietary supplement capsules due to substitution with toxic Yellow Oleander instead of the labeled ingredient Nuez de la India.
Product
NUT DIET MAX, Nuez de la India, Aleurites Moluccanus, 30 Capsules, 500mg Veggie Caps
Category
Food
Distribution
0 states