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.

9201–9225 of 9622

ModerateFDA (Devices)·Z-0184-2013·2012-11-07
Wright Medical Recalls Knee Components Due to Shelf Life Labeling Errors
Wright Medical Technology Inc is recalling 729 knee components due to potential inaccuracies in labeled shelf life at the Toulon, France facility.
Product
Knee Components: ROTULE "913" D=32 , Part Number PGA00030, Lot Number X02383380 INSERT TIBIAL "913 PCR" T.1 - EP.10-, PGA00050, Lot Numbers: V11272719, W02300988, W09372781, W09372781, and W10372876 INSERT TIBIAL "913 PCR" T.1 - EP.14-, PGA00054, Lot Number: V0266952 INSERT
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0185-2013·2012-11-07
Wright Medical Recalls Extremity Components Due to Shelf Life Labeling Errors
Wright Medical Technology Inc. is recalling 840 units of orthopaedic extremity components because the labeled shelf life may be inaccurate for products packaged in Toulon, France.
Product
Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM, Part Number PPO90000, Lot Numbers: U11113596, W12372884, W12376849, X01383482, X06391313, X07401148, X07401445, and X09418985 PROTHESE A EXPANSION COMPLETE D=8 LG 15 MM, Part Number PPO90100, Lot Number X0941898
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0188-2013·2012-11-07
Roche Recalls cobas 4800 BRAF V600 Mutation Test Kits
Roche Molecular Systems is recalling 44 kits of the cobas 4800 BRAF V600 Mutation Test because internal-use controls were incorrectly packaged into the product.
Product
cobas 4800 BRAF V600 Mutation Test for In Vitro Diagnostic Use Roche Molecular Systems, Inc., Product Usage: The primary use of the cobas 4800 BRAF V600 Mutation Test is the detection of the BRAF V600 mutations in DNA extracted from formalin-fixed, paraffin-embedded human me
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-0314-2013·2012-10-31
Pepper Jelly Recalled for Undeclared Milk and Soy Ingredients
Hanover Pike Enterprises is recalling 1,500 jars of Pepper Jelly because the product contains milk and soy, which are not listed on the label.
Product
Pepper Jelly, 4 and 8 ounce jars, labeled in part ***Jill's Jams &amp; Jellies, Hampstead, MD 21074***
Category
Food
Distribution
16 states
HighFDA (Devices)·Z-0139-2013·2012-10-31
Encore Medical Recalls 6.5mm Cancellous Bone Screws Due to Labeling Errors
Encore Medical is recalling 6.5mm Cancellous Bone Screws because some units were mislabeled with incorrect sizes, posing a risk of improper surgical fixation.
Product
6.5mm Cancellous Bone Screw Intended to be used for the fixation of the acetabular shell or fracture repair.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0327-2013·2012-10-31
General Mills Recalls Nature Valley Almond Granola Bars for Peanut Labeling Error
General Mills is voluntarily recalling Nature Valley Sweet & Salty Nut Almond granola bars because they may contain peanuts not listed on the label.
Product
Individual wrapper: Nature Valley Sweet & Salty Nut, granola bars, Peanut, net WT 1.2 oz (35 g) UPC 0 1600044282 5, Distributed by General Mills Sales, INC., Minneapolis, MN 55440. Ingredients: Roasted Peanuts, High Maltose Corn Syrup......, Mixed Tocopherols Added to Retain Fres
Category
Food
Distribution
2 states
HighFDA (Food)·F-0316-2013·2012-10-31
Peach Brandy Jam Recalled for Undeclared Milk and Soy Allergens
Hanover Pike Enterprises is recalling Peach Brandy Jam because it contains undeclared milk and soy ingredients.
Product
Peach Brandy Jam, 4 and 9 ounce jars, labeled in part ***Jill's Jams &amp; Jellies, Hampstead, MD 21074***
Category
Food
Distribution
16 states
HighFDA (Food)·F-0319-2013·2012-10-31
Buitoni Spinach Ravioli Recalled for Undeclared Shrimp and Lobster Allergens
Nestle Prepared Foods is recalling Buitoni Spinach & Portobello Mushroom Ravioli because it may contain undeclared shrimp and lobster.
Product
BUITONI brand Spinach & Portobello Mushroom All Natural Ravioli, packaged in an 18 oz. bag, frozen UPC code 24842-99186
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0313-2013·2012-10-31
Hanover Pike Enterprises Recalls Hot Pepper Jelly for Undeclared Allergens
Hanover Pike Enterprises is recalling 1,500 jars of Hot Pepper Jelly because the product contains undeclared milk and soy ingredients.
Product
Hot Pepper Jelly, 4 and 8 ounce jars, labeled in part ***Jill's Jams &amp; Jellies, Hampstead, MD 21074***
Category
Food
Distribution
16 states
ModerateFDA (Drugs)·D-019-2013·2012-10-31
Bristol-Myers Squibb Recalls Mislabelled Kombiglyze XR Physician Sample Cartons
Bristol-Myers Squibb is recalling specific lots of Kombiglyze XR physician sample cartons because the external packaging was incorrectly labeled as 2.5mg/1000mg, while the contents were 5mg/500mg.
Product
Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets, Physician Sample-Not For Sale, 7 Tablets per Carton, 5 mg/500 mg, Rx only, Manufactured By: Bristol-Myers Squibb Company, Princeton NJ 08543, USA, Marketed By: Bristol-Myers Squibb Company, Princeton NJ 08543
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-018-2013·2012-10-31
Bristol-Myers Squibb Recalls Mispackaged Kombiglyze XR Physician Sample Cartons
Bristol-Myers Squibb is recalling 117,049 physician sample cartons of Kombiglyze XR because some external cartons were mislabeled with the wrong dosage, though the individual blister units inside are correctly labeled.
Product
Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets, Physician Sample-Not For Sale, 6 Tablets per Carton, 2.5 mg/1000 mg, Rx only, Manufactured By: Bristol-Myers Squibb Company, Princeton NJ 08543, USA, Marketed By: Bristol-Myers Squibb Company, Princeton NJ 08
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0133-2013·2012-10-31
DePuy Mitek VAPR Hook Electrode Recalled for Incorrect Labeling
DePuy Mitek is recalling 376 VAPR Hook Electrodes because the packaging may display the wrong product identification label.
Product
DePuy Mitek VAPR Hook Electrode 3.5mm Hook Electrode with Integrated Handpiece Catalog Number: 227305 The DePuy Mitek VAPR Electrodes for use with the VAPR Radiofrequency System are intended for resection, ablation, excision, hemostasis of blood vessels, and coagulation of
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0024-2013·2012-10-31
Optovue Recalls Reference Materials Shipped with iVue and RTVue Systems
Optovue is recalling 795 units of reference materials shipped with iVue and RTVue systems because they were not included in the FDA clearance.
Product
Reference materials "RETINAL OCT Analysis and Interpretation Method" shipped with iVue System (K091404) and the "Retina Poster" shipped with iVue System (K091404) and RTVue Systems (K101505); Models: iVue-100, RTVue-100; The physical Product is manufactured and distributed by O
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0120-2013·2012-10-31
Ormco Recalls Damon 3MX Bicuspid Brackets Due to Misidentification
Ormco/Sybronendo is recalling 148 Damon 3MX Bicuspid Brackets because they were produced with incorrect dark blue ID dots instead of purple, leading to misidentification as maxillary central incisor brackets.
Product
The brand name of the device is Damon 3MX Bicuspid Bracket, an orthodontic bracket. Part Number 494-4491, Description -Damon 3MX Bicuspid Bracket, Lot Number - 011265039 Product Usage: Damon 3MX Bicuspid Brackets are intended to be a fixed attachment on a tooth which holds
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0110-2013·2012-10-31
Beckman Coulter Recalls Synchron Multi Calibrator Diskettes Due to Mislabeling
Beckman Coulter is recalling Synchron Multi Calibrator Diskettes because some units may be mislabeled as Thyroxine (T4) Reagent Calibrator Diskettes.
Product
Synchron Systems Synchron Calibrator Multi Calibrator Diskettes, Part Number 442600. The SYNCHRON MULTI-CALIBRATOR, used in conjunction with SYNCHRON reagents, is intended for use on SYNCHRON Systems for the calibration of Albumin, Blood Urea Nitrogen (Urea), Calcium, Choleste
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0079-2013·2012-10-24
Luigi's Italian Ice Birthday Cake Recalled for Dairy Mislabeling
J & J Snack Foods is recalling Luigi's Real Italian Ice Birthday Cake because it is mislabeled as 'Dairy-Free'.
Product
Luigi's Real Italian Ice Birthday Cake 6 FL OZ cups Net Wt 36 FL OZ (1.06 L) upc 73321-04418 J & J Snack Foods Corp. Pennsauken, NJ 08109 USA at Plant #42-2479 www.luigis.com
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0056-2013·2012-10-24
Beckman Coulter AutoMate 1250 and 2550 Sample Processing System Recall
Beckman Coulter is recalling AutoMate 1250 and 2550 systems due to a risk of sample misidentification caused by duplicate barcode labels.
Product
AutoMate 1250 and AutoMate 2550, Part Numbers ODL25125 and ODL25255. The AutoMate 1200/2500 System Series is a semi-open, pre- and post-analytical sample processing and sorting system. The base system automates the sample sorting, decapping, and archiving processes. Handling a
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0119-2013·2012-10-24
Ralcorp Blueberry Muffins Recalled for Undeclared Tree Nuts
Ralcorp is recalling blueberry muffins that may contain undeclared tree nuts due to mislabeling.
Product
GFS Individually Wrapped Blueberry Muffins, 1.8 Ounce, in 80 count case, Net Weight 9 lb./4.1 kg; Manufactured for Gordon Food Service, Grand Rapids, MI 40546; UPC 0 009390-157700 9 Please note: there is no labeling on the individual muffin wrappers other than the code date.
Category
Food
Distribution
3 states
HighFDA (Food)·F-0298-2013·2012-10-24
Alden's Cookies and Cream Ice Cream Recalled for Undeclared Wheat
Oregon Ice Cream, LLC is recalling Alden's Cookies and Cream ice cream because wheat was not declared on the label.
Product
Alden's Cookies and Cream is an ice cream product. It is packaged in a 1.5 quart (48 oz) cup. The LID of the recalled product is labeled in parts:"***ORGANIC***Alden's ICE CREAM***COOKIES 'n CREAM***1.5 QTS (1.42L)***". The CUP of the recalled product is labeled in parts:
Category
Food
Distribution
7 states
ModerateFDA (Devices)·Z-0082-2013·2012-10-24
Aesculap Recalls Two Columbus Femoral Cutting Guides Due to Marking Error
Aesculap, Inc. is recalling two Columbus 4-IN-1 Femoral Cutting Guide Instruments because the laser markings for size identification are incorrect, although the instruments are correctly dimensioned.
Product
Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)
Category
Medical Device
Distribution
2 states
ModerateFDA (Food)·F-0123-2013·2012-10-24
Southwind Foods Recalls Frozen Snapper Fill IQF for Mislabeling
Southwind Foods is recalling 145 cases of frozen snapper fill IQF because the product was mislabeled and misleading.
Product
Frozen Red Cod Fillet (Red Snapper) Individually Quick Frozen was labeled and identified as Snapper FILL IQF (ROCKFISH). 1/10 lb, code #14343.
Category
Food
Distribution
3 states
ModerateFDA (Devices)·Z-0061-2013·2012-10-24
Zimmer Recalls CPT Hip Stems Due to Incorrect Packaging
Zimmer, Inc. is removing CPT Hip System femoral stems from the market because they were packaged in incorrect cartons and distributed internationally and domestically.
Product
CPT Hip System Femoral Stem Petite, Item No. 00-8011-000-05. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
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
ModerateFDA (Devices)·Z-0081-2013·2012-10-24
Boston Scientific Recalls Leveen Coaccess Introducer Sets for Incorrect Portuguese Instructions
Boston Scientific is recalling 19,716 Leveen Coaccess Introducer Sets because the Portuguese instructions for use contain errors. The devices were distributed in Brazil, Portugal, and Hong Kong.
Product
Leveen Coaccess Introducer Set. 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 nonresectable liver lesions.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-0062-2013·2012-10-24
Zimmer Recalls CPT Hip Stems Due to Incorrect Packaging Cartons
Zimmer Inc. is removing CPT hip stems from the market because they were packaged in incorrect cartons and distributed domestically and internationally.
Product
CPT Femoral Stem 12/14 Neck Taper Extended Offset,(item 00-8114-001-10. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide