Hazard

Mis Labeling recalls

9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 9,622
Critical: 163
Severe: 590
Most recent: 2026-09-24

Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (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.

9226–9250 of 9622

ModerateFDA (Devices)·Z-0080-2013·2012-10-24
Boston Scientific Recalls Leveen Needle Electrodes Due to Incorrect Portuguese Instructions
Boston Scientific is recalling Leveen Coaccess Needle Electrodes because the Portuguese instructions for use contain errors. The recall affects units distributed in Brazil, Portugal, and Hong Kong.
Product
Leveen Coaccess Needle Electrode (3.5/15) and (4.0/15). Disposable, monopolar, electrosurgical devices, intended for use in conjunction with BSC radiofrequency generator for the thermal coagulation necrosis of soft tissues, including partial or complete ablation of nonresect
Category
Medical Device
Distribution
0 states
ModerateFDA (Food)·F-0121-2013·2012-10-24
Pepsi Beverages Recalls Mislabeled Diet Crush Orange Soda Cans
Pepsi Beverages Company is recalling 1,791 cases of Diet Crush Orange Soda in Arizona due to mislabeling involving new graphics on the previous formulation.
Product
Diet Crush Orange Soda, 12 oz cans
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-0295-2013·2012-10-24
Sun Boricua Pa'l Mundo Recalls Marlin-Filled Turnovers for Undeclared Color Additives
Sun Boricua Pa'l Mundo Inc. is recalling 36,000 units of Marlin-filled turnovers in Puerto Rico due to undeclared color additives.
Product
"Tacos de Marlin" (Marlin-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebrada, Camuy PR 00627
Category
Food
Distribution
1 state
ModerateFDA (Drugs)·D-009-2013·2012-10-24
Earthborn Products Recalls Colloidal Silver Supplement for Lack of FDA Approval
Earthborn Products is recalling 161 gallons of colloidal silver supplements because the FDA determined the product is misbranded and not generally recognized as safe and effective.
Product
Colloidal Silver, 100 ppm TDS, Natural Mineral Supplement, sold in a) 2 fl.oz (59.15 mL), b) 8 fl.oz (236.6 mL), c) 16 fl.oz (473.2 mL), d) 32 fl.oz (946.4 mL), e) 64 fl.oz (1.89 L), and f) 1 Gal. (3.78 L), Distributed by: Earthborn Products, San Diego, CA 92103.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0079-2013·2012-10-24
Boston Scientific Recalls LeVeen Needle Electrode Systems for Incorrect Portuguese Instructions
Boston Scientific is recalling LeVeen Standard Needle Electrode Systems because the Portuguese instructions for use are incorrect. The recall affects units distributed in Brazil, Portugal, and Hong Kong.
Product
LeVeen Standard Needle Electrode System, Sterile (3.5/12), (3.5/15), (4.0/15), (3.5/25), (5.0/15), (5.0/25), and (4.0/25). Disposable, monopolar, electrosurgical devices, intended for use in conjunction with BSC radiofrequency generator for the thermal coagulation necrosis of
Category
Medical Device
Distribution
0 states
CriticalFDA (Food)·F-0028-2013·2012-10-17
FDA Recalls Organic Pine Nuts Due to Potential Peanut Contamination
Newark Nut Stores is recalling 870 lbs of organic pine nuts nationwide because they may contain peanuts.
Product
Organic Pine Nuts (Raw, No Shell) 1 lb.Nuts.com NutsOnline, 125 Moen Street, Cranford, NJ 07016 800-558-8881
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0053-2013·2012-10-17
Dae Han Tofu Soya Select Stir Fried Tofu Recalled for Labeling Error
Pacific Northwest Tofu, LLC is recalling Dae Han Tofu Soya Select Stir Fried Tofu because soy was partially declared on the label due to a printing error.
Product
Stir Fried Tofu is packaged in a retail vacuum plastic package and each has net wt. 7.5 oz.. The product is sold under the Dae Han Tofu Soya Select brand. Stir Fried Tofu has the UPC 0 31499 003283.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0047-2013·2012-10-17
Beckman Coulter Recalls Access Folate Calibrators Due to Falsely Elevated Results
Beckman Coulter is recalling Access Folate Calibrators because they may produce falsely elevated results that could mask a folate deficiency.
Product
Access Folate WHO Calibrators, Part Number: A98033. The Access Folate Calibrators are intended to calibrate the Access Folate assay using the Access Immunoassay Systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0024-2013·2012-10-17
Neera's Tikka Curry Sauce Recalled for Undeclared Milk and Soy
Cinnabar Specialty Foods is recalling Neera's Tikka Curry Simmering Sauce because it contains undeclared milk and soy ingredients.
Product
Neera's Tikka Curry Rich and Creamy All Natural Simmering Sauce, 16 fluid ounces/ 473 ml. Packaged in jar. Packaged at 12/16oz units/case. Product labeling reads in part:" NEERA'S TIKKA CURRY Rich and Creamy All Natural Simmering Sauce***Just add meat, fish or vegetables!***16
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0042-2013·2012-10-17
IDS-iSYS Osteocalcin Assay Recalled for Incorrect IVD Labeling
Immunodiagnostics Systems Ltd is recalling IDS-iSYS N-Mid Osteocalcin assays because they were labeled as In Vitro Diagnostics (IVD) despite not being registered for that use in the US.
Product
IDS-iSYS N-Mid¿ Osteocalcin, Catalog Number IS-2900. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS N-Mid¿ Osteocalcin Assay is intended for the quantitative determination of Osteocalcin in human serum or plasma on the IDS-iSYS Multi-Discipline Automated Anal
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0041-2013·2012-10-17
IDS-iSYS Ostase BAP Control Set Recalled for Incorrect Labeling
Immunodiagnostics Systems Ltd is recalling IDS-iSYS Ostase BAP Control Sets because they are labeled as IVDs but are not registered for that use in the US.
Product
IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Control Set, Catalog Number IS-2830. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS Ostase¿ BAP (IDS-iSYS BAP) Control Set is used for quality control of the IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Ass
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0096-2013·2012-10-17
Da Vinci Pesto Genovese Recalled for Mislabeling Omitted Pine Nuts
World Finer Foods is recalling Da Vinci Pesto Genovese because pine nuts are listed on the front label but omitted from the ingredient statement.
Product
Da Vinci Pesto Genovese with basil and pine nuts Net Wt. 10 oz. (283 g) Distributed by World Finer Foods, Inc. Bloomfield, NJ 07003 Product is packaged in a glass jar with lid. www.worldfiner.com Product of Italy UPC: 0 70670-00822 4
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0040-2013·2012-10-17
Immunodiagnostics Systems Recalls IDS-iSYS Ostase BAP Assay Due to Labeling Error
Immunodiagnostics Systems Ltd is recalling IDS-iSYS Ostase BAP assays because they were labeled for in vitro diagnostic use despite not being registered for that purpose in the US.
Product
IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase), Catalog Number IS-2800. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS Ostase¿ BAP Assay (IDS-iSYS BAP) is intended for the quantitative determination of bone-specific alkaline phosphatase (BAP), an indicator
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0052-2013·2012-10-17
Pacific Northwest Tofu Recalls Teriyaki Tofu for Labeling Error
Pacific Northwest Tofu, LLC is recalling 32 packages of Dae Han Tofu Soya Select Teriyaki Tofu because the soy ingredient declaration is partially cut off on the label.
Product
Teriyaki Tofu is packaged in a retail vacuum plastic package and each has net wt. 7.5 oz.. The product is sold under the Dae Han Tofu Soya Select brand. The Teriyaki Tofu has the UPC 0 34199 718965.
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-0043-2013·2012-10-17
IDS-iSYS N-Mid Osteocalcin Control Set Recalled for Labeling Errors
Immunodiagnostics Systems Ltd is recalling IDS-iSYS N-Mid Osteocalcin Control Sets because they were labeled as IVDs instead of Research Use Only.
Product
IDS-iSYS N-Mid¿ Osteocalcin, Catalog Number IS-2930. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS N-Mid¿ Osteocalcin Control Set is used for quality control of the IDS-iSYS N-Mid¿ Osteocalcin Assay on the IDS-iSYS Multi-Discipline Automated Analyser.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0051-2013·2012-10-17
Pacific Northwest Tofu Recalls Hot & Spicy Tofu Due to Labeling Error
Pacific Northwest Tofu, LLC is recalling 10 packages of Hot & Spicy Tofu because the ingredient list is cut off, partially declaring wheat or sesame seed oil.
Product
Hot & Spicy Tofu is packaged in a retail vacuum plastic package and each has net wt. 7.5 oz.. The product is sold under the Dae Han Tofu Soya Select brand. Hot & Spicy Tofu has the UPC 0 34199 719191.
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-0029-2013·2012-10-17
Alere Recalls Triage TOX Drug Screen Kits Due to Mislabeled Boxes
Alere San Diego, Inc. is recalling Triage TOX Drug Screen kits because the boxes containing the test devices were mislabeled.
Product
Triage TOX Drug Screen Panel, Model# 94400. Product Usage: The Triage TOX Drug Screen is a fluorescence immunoassay intended to be used with the Triage Meters for the point-of-care qualitative determination of the presence of drug and/or the major metabolites above the thre
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0095-2013·2012-10-17
Pepsi Bottling Group Recalls Diet Orange Crush Due to Undeclared Corn Syrup
Pepsi Bottling Group Nashville is recalling 2-liter bottles of Diet Orange Crush because they contain undeclared high fructose corn syrup.
Product
diet Orange Crush, no calorie orange soda, 2 L (2.1 QT), UPC 078000013979
Category
Food
Distribution
4 states
ModerateFDA (Devices)·Z-0044-2013·2012-10-17
IDS-iSYS Intact PINP Assay Recalled for Incorrect IVD Labeling
Immunodiagnostics Systems Ltd is recalling IDS-iSYS Intact PINP assays because they were labeled for In Vitro Diagnostic use but are not registered for that purpose in the US.
Product
IDS-iSYS Intact PINP, Catalog Number IS-4000. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS Intact amino-terminal propeptide of type I procollagen (Intact PINP) assay is intended for the quantitative determination of intact PINP in human serum or plasma on t
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0035-2013·2012-10-17
Beckman Coulter Recalls TetraCXP Software for Labeling Updates
Beckman Coulter is recalling TetraCXP software and CYTO-STAT reagents to update specimen stability claims in the product labeling.
Product
TetraCXP Software System, Part Number A40051. Allows simultaneous identification and enumeration of total CD3+, total CD4+, total CD8+, dual CD3+/CD4+, dual CD3+/CD8+ and/or total CD3+, CD19+ and CD3+/CD56+ lymphocyte percentages and absolute counts in whole blood by flow cyto
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0034-2013·2012-10-17
Beckman Coulter Recalls CYTO-STAT Reagents Due to Labeling Stability Claims
Beckman Coulter is recalling CYTO-STAT tetraCHROME reagents because stability claims in the product labeling need to be updated to align with current standards.
Product
CYTO-STAT tetraCHROME CD45- FITC/CD56-RD1/CD19-ECD/CD3-PC5, Part Number 6607073. Allows simultaneous identification and enumeration of total CD3+, total CD4+, total CD8+, dual CD3+/CD4+, dual CD3+/CD8+ and/or total CD3+, CD19+ and CD3+/CD56+ lymphocyte percentages and absolute c
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0039-2013·2012-10-17
IDS Urine BETA CrossLaps ELISA Recalled for Incorrect IVD Labeling
Immunodiagnostics Systems Ltd is recalling IDS Urine BETA CrossLaps ELISA kits because they were labeled for in vitro diagnostic use despite not being registered for that purpose in the US.
Product
IDS Urine BETA CrossLaps ELISA, Catalog Number AC-05F1. Type of packaging: Cardboard Box containing plastic bottles. The Urine BETA CrossLaps¿ ELISA is an enzyme immunological test for the quantification of degradation products of C-terminal telopeptides of Type-I collagen in
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0033-2013·2012-10-17
Beckman Coulter Recalls CYTO-STAT Reagents Due to Labeling Updates
Beckman Coulter is recalling CYTO-STAT tetraCHROME reagents because stability claims in the product labeling need to be updated to align with current standards.
Product
CYTO-STAT tetraCHROME CD45-FITC/CD4-RD1/CD8-ECD/CD3-PC5, Part Number 6607013. Allows simultaneous identification and enumeration of total CD3+, total CD4+, total CD8+, dual CD3+/CD4+, dual CD3+/CD8+ and/or total CD3+, CD19+ and CD3+/CD56+ lymphocyte percentages and absolute co
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0045-2013·2012-10-17
IDS-iSYS Intact PINP Control Set Recalled for Incorrect IVD Labeling
Immunodiagnostics Systems Ltd is recalling 29 units of IDS-iSYS Intact PINP Control Set because they were labeled as In Vitro Diagnostics (IVD) despite not being registered for that use in the US.
Product
IDS-iSYS Intact PINP Control Set, Catalog Number IS-4030. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS Intact amino-terminal propeptide of type I procollagen (Intact PINP) Control Set is used for quality control of the IDS-iSYS Intact PINP Assay on the IDS-
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0050-2013·2012-10-17
Pacific Northwest Tofu Recalled for Incomplete Soy Labeling
Pacific Northwest Tofu, LLC is recalling Dae Han Tofu Soya Select Gourmet Firm Tofu because the ingredient list is cut off, partially declaring soy.
Product
Gourmet Firm Tofu is packaged in a retail vacuum plastic package and each has net wt. 7.5 oz.. The product is sold under the Dae Han Tofu Soya Select brand. The UPC is 0 34199 718903;
Category
Food
Distribution
1 state