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.

9001–9025 of 9622

HighFDA (Devices)·Z-0560-2013·2012-12-26
GE Healthcare Recalls Advantage Workstation Software Due to Vessel Label Mismatch
GE Healthcare is recalling specific Advantage Workstation software versions due to a potential vessel label mismatch and a measurement tool refresh issue that may impact patient safety.
Product
Advantage Workstation Volume Share 2 (versionAW4.4_04) with Volume Viewer 3 and 3.1 (version7.0 to version7.5 and version 8.1) and only when or more of these applications is installed: " VesselIQ Xpress or AVA Xpress " CardIQ Xpress Pro or Plus " CardEP " CardIQ Fusion PET or
Category
Medical Device
Distribution
31 states
HighFDA (Food)·F-0835-2013·2012-12-26
Lobster Base Recalled for Missing Milk Allergen Labeling
Williams West & Witt's is recalling specific lobster base products because the labels failed to identify milk as an ingredient, posing a risk to consumers with milk allergies.
Product
#124-M Primarque Lobster Base, Net Weight (1LB) 454 G & 50 Pounds (22.68 kg) Packed for Primarque Products, Worcester, MA 01610 #124-M Cook's Delight Lobster Base, Net Weight (1LB) 454 G & 50 Pounds (22.68 kg) Packed By Integrative Flavors, Michigan City, Indiana 46360 #124-M
Category
Food
Distribution
6 states
HighFDA (Food)·F-0842-2013·2012-12-26
Cook's Delight Lobster Base Recalled for Undeclared Milk Allergen
Williams West & Witt's Products Company is recalling Cook's Delight Lobster Base because the label failed to identify milk as an ingredient. Consumers with a milk allergy are at risk of serious allergic reactions.
Product
#226 Cook's Delight Lobster Base, Net Weight 30 Pounds; 5 Pounds, Packed by Integrative Flavors, Michigan City, Indian
Category
Food
Distribution
6 states
HighFDA (Food)·F-0839-2013·2012-12-26
Shrimp Base Recalled for Undeclared Milk Allergen
Williams West & Witt's Products Company is recalling Cook's Delight Shrimp Base because the label failed to identify milk as an ingredient.
Product
#428N Cook's Delight Shrimp Base, Net Weight 50 Pounds (22.68 kg) Packed by Integrative Flavors, Michigan City, Indiana
Category
Food
Distribution
6 states
HighFDA (Food)·F-0840-2013·2012-12-26
Mushroom Base Recalled for Missing Milk Allergen Labeling
Williams West & Witt's Products Company is recalling Cook's Delight Mushroom Base because the label failed to identify milk as an ingredient, posing a risk to consumers with milk allergies.
Product
#272N Cook's Delight Mushroom Base, Net Weight 50 Pounds (22.68 kg) Packed by Integrative Flavors, Michigan City, Indiana 46360
Category
Food
Distribution
6 states
HighFDA (Food)·F-0845-2013·2012-12-26
Newman's Own Lite Honey Mustard Dressing Recalled for Missing Milk Allergen Label
Newman's Own Inc. is recalling Lite Honey Mustard Dressing because the label failed to list milk as an allergen.
Product
Newman's Own Lite Honey Mustard Dressing, 16 FL.OZ (473 mL)
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0834-2013·2012-12-26
Primarque Clam Base Recalled for Undeclared Milk Allergen
Williams West & Witt's Products Company is recalling Primarque Clam Base because the label failed to identify milk as an ingredient, posing a risk to consumers with milk allergies.
Product
#223-E Primarque Clam Base, Net Weight 50 pounds (22.68 kg) Packed for Primarque Products, Worcester, MA 01610
Category
Food
Distribution
6 states
HighFDA (Food)·F-0851-2013·2012-12-26
Riviana Recalls Yellow Rice Mixes for Undeclared Soy Protein
Riviana International is recalling specific Shurfine and Hannaford yellow rice mixes because they contain undeclared hydrolyzed soy protein.
Product
Yellow rice mixes with the following g brand names: (1) Shurfine brand Yellow Rice with Saffron, NET WT 5 OZ (142g), distributed by TOPCO ASSOCIATES, LLC, 7711 GROSS POINT ROAD, SKOKIE, IL 60077. UPC 011161159834 and (2) Hannaford brand Yellow Rice with real saffron & other sea
Category
Food
Distribution
4 states
HighFDA (Food)·F-0844-2013·2012-12-26
Crab Base Products Recalled for Undeclared Milk Allergen
Williams West & Witt's recalls Primarque and Cook's Delight crab base products because the labels failed to identify milk as an ingredient, posing a risk to consumers with milk allergies.
Product
#321N Primarque Crab Base, Net Weight 50 Pounds, Packed For Primarque Products, Worcester, MA 01610 #321 N Cook's Delight,Crab Base, Net Weight 50 Pounds, Packed By Integrative Flavors, Michigan City, Indiana 46360
Category
Food
Distribution
6 states
HighFDA (Food)·F-0836-2013·2012-12-26
Seafood Base Recalled for Undeclared Milk Allergen
Williams West & Witt's is recalling Primarque and Cook's Delight Seafood Base because the label failed to identify milk as an ingredient.
Product
#126 Primarque Seafood Base, Net Weight 16 oz, 1LB, 454 G & 50 Pounds (22.68 kg) Packed for Primarque Products, Worcester, MA 01610 #126 Cook's Delight Seafood Base, Net Weight 16 oz (1LB) 454 G & 50 Pounds (22.68 kg) Packed By Integrative Flavors, Michigan City, Indiana 46360
Category
Food
Distribution
6 states
HighFDA (Food)·F-0841-2013·2012-12-26
Cook's Delight Shrimp Base Recalled for Undeclared Milk Allergen
Williams West & Witt's Products Company is recalling Cook's Delight Shrimp Base because the label failed to identify milk as an ingredient, posing a risk to consumers with milk allergies.
Product
#828 Cook's Delight Shrimp Base, Net Weight 30 Pounds; 5 Pounds, Packed by Integrative Flavors, Michigan City, Indian
Category
Food
Distribution
6 states
HighFDA (Food)·F-0838-2013·2012-12-26
Williams West & Witt's Recalls Clam Base for Unlabeled Milk Allergen
Williams West & Witt's is recalling Primarque Clam Base because the label failed to identify milk as an ingredient. Consumers with milk allergies are at risk of serious allergic reactions.
Product
#822- M PrimarqueClam Base, Net Weight 50 Pounds (22.68 kg) Packed for Primarque Products, Worcester, MA 01610
Category
Food
Distribution
6 states
HighFDA (Food)·F-0832-2013·2012-12-26
Clam Base Products Recalled for Undeclared Milk Allergen
Williams West & Witt's is recalling Clam Base products because the ingredient label failed to identify milk, a major allergen, as a source of butter and cream.
Product
#122-A, Piazza Produce Clam Base, Net Weight 16 oz (1 lb) 454G Packed For: Piazza Produce, Indianapolis, IN 46268: #122-A, Primarque Clam Base, Net Wt 16 oz (1 lb) 454 grams Manufactured for Primarque Products Co. Worcester, MA 01610 #122-A, Clam Base, Cook's Delight Clam
Category
Food
Distribution
6 states
HighFDA (Food)·F-0843-2013·2012-12-26
Primarque Lobster Base Recalled for Undeclared Milk Allergen
Williams West & Witt's is recalling Primarque Lobster Base because the label failed to identify milk as an ingredient, posing a risk to consumers with milk allergies.
Product
#326 RS PrimarqueLobster Base, Net Weight 50 Pounds;, PackedFor Primarque Products, Worcester, MA 01610
Category
Food
Distribution
6 states
HighFDA (Food)·F-0837-2013·2012-12-26
Primarque Fish Base Recalled for Undeclared Milk Allergen
Williams West & Witt's is recalling Primarque Fish Base because the label failed to identify milk as an ingredient, posing a risk to consumers with milk allergies.
Product
#425N Primarque Fish Base, Net Weight 50 Pounds (22.68 kg) Packed for Primarque Products, Worcester, MA 01610
Category
Food
Distribution
6 states
ModerateFDA (Food)·F-0846-2013·2012-12-26
Arnold's Candies Wintergreen Puffs Recalled for Missing Color Additives on Label
Arnold's Candies Wintergreen Puffs are being recalled because the label failed to list Yellow #5 and Blue #1. The product was distributed in New York, Ohio, and Pennsylvania.
Product
Arnold's Candies Handmade Since 1953 www.arnoldscandies.com Wintergreen Puffs***INGREDIENTS: Sugar, Cream of Tarter, Artificial Flavoring and Coloring WARNING: Manufactured in a facility that also handles peanuts NET WT 6 oz (170g) 0 73629 00308 0 931 High Grove Blvd Akron, OH 4
Category
Food
Distribution
3 states
ModerateFDA (Devices)·Z-0526-2013·2012-12-26
EEG Info Recalls EEG NeuroAmp Devices Due to Mislabeling
EEG Info is recalling EEG NeuroAmp devices because of a potential risk associated with mislabeling.
Product
EEG NeuroAmp, Model Number: CS 10090; CS 10137. Biofeedback and Relaxation
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0568-2013·2012-12-26
Medline Angio Drape Pack Recall Due to Sterility Misidentification
Medline is recalling 105 Angio Drape Packs because a non-sterile waste bag was assumed to be sterile by customers.
Product
Medline Angio Drape Pack Radiology-LF; a sterile custom single patient prescription procedure pack, including a waste bag, for use by the Interventional Radiology Department; Packaged for Medline Industries, Inc.; Reorder #DYNJ35993D This custom pack includes components necess
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0847-2013·2012-12-26
Arnold's Candies Root Beer Puffs Recalled for Missing Color Labeling
Arnold's Candies is recalling Root Beer Puffs because the label failed to list Yellow #5 and Blue #1. The product was distributed in New York, Ohio, and Pennsylvania.
Product
Arnold's Candies Handmade Since 1953 www.arnoldscandies.com Root Beer Puffs Puffs***INGREDIENTS: Sugar, Cream of Tarter, Artificial Flavoring and Coloring WARNING: Manufactured in a facility that also handles peanuts NET WT 6 oz (170g) 0 73629 00307 3 931 High Grove Blvd Akron,
Category
Food
Distribution
3 states
ModerateFDA (Devices)·Z-0565-2013·2012-12-26
Del Mar Reynolds Medical Recalls BleaseFocus Anesthesia Workstations Due to Manual Error
Del Mar Reynolds Medical is recalling BleaseFocus Anesthesia Workstations and 700/900 Series Ventilators because the user manuals describe a secondary oxygen supply failure alarm that is not actually installed in the devices.
Product
BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators are anesthesia gas machine. In most cases, the customer ordered both a BleaseFocus anesthesia workstation and a 700/900 ventilator. In some cases, the customer may order a 700/900 stand-alone ventilator would co
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0569-2013·2012-12-26
DePuy Recalls Pinnacle Cancellous Screws Due to Labeling Error
DePuy Orthopaedics is recalling 118 Pinnacle Cancellous Screws because the labels incorrectly identify them as Cannulated Screws.
Product
Pinnacle Cancellous Screw Packaging: Product is housed within a polyurethane protector; this is placed inside an uncoated Tyvek/PET peel pouch and sealed. This package is placed into a paperboard carton, labeled and shrink-wrapped. PINNACLE¿ CANCELLOUS Bone Screws are ancil
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0529-2013·2012-12-26
DePuy Mitek Sterile Reamers Recalled for Incorrect Size Labeling
DePuy Mitek is recalling 20 sterile reamers because 7 units were labeled as 11MM but contained 10MM reamers.
Product
DePuy Mitek 11 MM Fully Fluted Reamer, Sterile Product Number: 232423 DePuy Mitek Sterile Reamers are intended to cut through cortical and cancellous bone during Cruciate Ligament Repair/Reconstruction of the knee.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0535-2013·2012-12-26
Titan Spine Recalls Endoskeleton TA VBR Implants for Labeling Errors
Titan Spine is recalling 92 Endoskeleton TA VBR implants because their labels contain incorrect indications for use.
Product
Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard Endoskeleton Implant VBR 2107-0120 20mm Standard Endoskeleton Implant VBR 2107-0218 18mm Large Endoskeleton Implant VBR 2107-0220 20mm Large Endoskeleton Implant VBR Endoskeleton TA VBR is intended
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0527-2013·2012-12-26
Biomet Recalls EBI XFIX DFS Rail System Due to Missing Markings
Biomet is recalling 49 units of the EBI XFIX DFS Rail System because graduation markings were missing on 14 swivel clamps.
Product
EBI XFIX DFS Rail System (Adult Rail Gradual Swivel Clamp). The Biomet Rail System consists of a unilateral external fixator rail, modular bone screw clamps, and compression and distraction units. The device is used in the treatment of bone fractures.
Category
Medical Device
Distribution
7 states
LowFDA (Drugs)·D-097-2013·2012-12-26
Genentech Recalls CellCept Capsules Due to Short Fill Issues
Genentech is recalling 1,128 bottles of CellCept (mycophenolate mofetil) 250 mg capsules because some bottles contained fewer than 120 capsules as labeled.
Product
CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles per carton, NDC 0004-0259-05; b) 120-count capsules per bottle, NDC 0004-0259-51; Made in Ireland; Distributed by: Genentech USA, Inc., South San Francisco, CA 94080.
Category
Drug
Distribution
Distributed nationwide