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.

9401–9425 of 9622

CriticalFDA (Devices)·Z-2062-2012·2012-08-22
Stryker Neptune 1 Gold Rover Waste Management System Recalled for Injury Risk
Stryker is recalling Neptune 1 Gold Rover waste management systems due to reports of serious injury and a fatality associated with the Neptune 2 system.
Product
Neptune 1 Gold Rover (120 Vand 230V ) Waste Management System Part Number 0700-001-000, 0700-002-000(International) Instructions For Use 0700-001-700, 0700-002-707 Intended for use in the surgical environment or physician's office to collect and dispose of surgical fluid was
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1943-2012·2012-08-22
Baroody Imports Recalls Chiclets Chewing Gum for Unsafe Color Additives
Baroody Imports Inc. is voluntarily recalling Chiclets Chewing Gum (Fruit Flavors) due to misbranded and unsafe color additives.
Product
Chiclets Chewing Gum Fruit Flavors; Made in Lebanon; Manufactured by Cadbury Adams Middle East S.A.L.
Category
Food
Distribution
6 states
ModerateFDA (Devices)·Z-2201-2012·2012-08-22
Nico BrainPath Sheath Recall Due to Incorrect Length Labeling
Nico Corp. is recalling 15 BrainPath sheaths because 50mm units were mislabeled as 60mm, causing improper fit.
Product
13.5 mm x 60 mm BrainPath Sheath The NICO BrainPath is a family of products that consists of multiple sized reusable and re-sterilizable obturators with coordinating single patient use, disposable sheaths (three lengths available for each: 50mm, 60mm, and 75mm). The obturator
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-2187-2012·2012-08-22
Zimmer Recalls NCB Polyaxial Locking Plate System NCB Screws Due to Incorrect Size
Zimmer, Inc. is recalling 26mm NCB Polyaxial Locking Plate System screws because a lot contained incorrect 32mm screws.
Product
The NCB Polyaxial Locking Plate System NCB screws 26mm: 02.03155.026, non-sterile Product is implantable screws indicated for temporary internal fixation and stabilization of fractures and osteotomies of long bones. These screws are intended for bicortical anchorage.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2211-2012·2012-08-22
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products DGXN Slides
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products DGXN Slides because the Instructions for Use were revised to remove heparin plasma as a recommended specimen type.
Product
VITROS Chemistry Products DGXN Slides --- [REF] 834 3386. Product is packaged in a box with multiple slides. The lot and expiration codes are found on the side of the package. Product Usage: Intended use: For in vitro diagnostic use only. VITROS Chemistry Products DGXN Sli
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2200-2012·2012-08-22
Nico BrainPath Sheaths Recalled for Incorrect Length Labeling
Nico Corp. is recalling 20 BrainPath sheaths because 50mm units were mislabeled as 60mm, creating a risk of improper fit during use.
Product
13.5 mm x 50 mm BrainPath Sheath The NICO BrainPath is a family of products that consists of multiple sized reusable and re-sterilizable obturators with coordinating single patient use, disposable sheaths (three lengths available for each: 50mm, 60mm, and 75mm). The obturator
Category
Medical Device
Distribution
1 state
LowFDA (Devices)·Z-2186-2012·2012-08-22
Teleflex Medical Recalls TAUT Cholangiogram Catheter Intraducer Due to Missing Label
Teleflex Medical is recalling 611 units of TAUT Cholangiogram Catheter Intraducers because the internal packaging is missing labels. The devices were distributed to 27 states.
Product
TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body.
Category
Medical Device
Distribution
26 states
LowFDA (Devices)·Z-2218-2012·2012-08-22
Terumo Sarns System 8000 Base Recalled for Incorrect Amperage Labeling
Terumo is recalling three Sarns System 8000 bases because they were distributed with incorrect amperage ratings on the nameplate labels.
Product
System 8000 Base Product Usage: The Sarns Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified medical profe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1645-2012·2012-08-22
Topiramate Tablets Recalled for Incorrect Labeling of Product Form
American Health Packaging is recalling Topiramate Tablets due to a labeling error that incorrectly identifies the product as capsules.
Product
Topiramate Tablets, 50 mg, 30-count (3 x 10) unit-dose blisters per carton, Rx only, Mfd by: Cadila Healthcare Ltd., Ahmedabad, India; Dist By: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534, Pkg by: American Health Packaging, Col. OH 43217, NDC 68084-343-21, blister barco
Category
Drug
Distribution
Distributed nationwide
LowNHTSA·12T023000·2012-08-17
Vogue Tires Recalled for Missing Tire Identification Numbers
Vogue Tyre & Rubber Company is recalling certain Custom Built and Signature V tires because they lack the required tire identification number on the sidewall.
Product
TIRES:MARKINGS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1860-2012·2012-08-15
Tres Monjitas Tropical Splash Acerola Recalled for Undeclared Allergens
Altura Food, Inc. is recalling 15 oz bottles of Tres Monjitas Tropical Splash Acerola because they contain undeclared allergens: hydrogenated coconut oil, sodium caseinate, and soy lecithin.
Product
"***Tres Monjitas***Tropical Splash***Acerola***15 oz***"
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-2164-2012·2012-08-15
Radiometer ABL90 FLEX Software Recall for HL7 Data Transmission Errors
Radiometer America Inc. is recalling ABL90 FLEX software version 2.7 MR3 because a data transfer error can cause mixed-up results when transmitting to hospital systems.
Product
ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer is intended for in vitro testing of samples of heparinized whole blood.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1842-2012·2012-08-15
Punjabi Cookies Recalled for Potential Undeclared Milk Allergen
Shah Distributors is recalling CRISPY Just Baked Punjabi Cookies because they may not declare milk as an ingredient.
Product
CRISPY Just Baked Punjabi Cookies 800 g/1.76 lb (28.2 oz): Product of Canada Manufactured by: TWIK Foods Inc. Mississauga, ON, Canada.
Category
Food
Distribution
1 state
HighFDA (Food)·F-1928-2012·2012-08-15
Designer Whey Strawberry Protein Powder Recalled for Gluten Contamination
Designer Protein LLC is recalling Designer Whey Strawberry protein powder because lab tests found gluten in products labeled gluten-free.
Product
Designer Whey Strawberry, 2lbs, Item#10200137, 4 units/case. UPC 8-44334-00137-7.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1927-2012·2012-08-15
Designer Whey French Vanilla Protein Powder Recalled for Gluten
Designer Protein LLC is recalling Designer Whey French Vanilla protein powder because lab results confirmed the presence of gluten in products labeled gluten-free.
Product
Designer Whey French Vanilla, 2lbs, item # 10200133, 4 units/case. UPC 8-44334-00133-9. Designer Whey French Vanilla, 3lbs, Item#10200134, 5 units/case. UPC 8-4434-00133-10.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1926-2012·2012-08-15
Designer Whey Chocolate Protein Powder Recalled for Gluten Contamination
Designer Protein LLC is recalling Designer Whey Chocolate protein powder because lab tests found gluten in products labeled gluten-free.
Product
Designer Whey Chocolate, 2lbs, item#10200131, 4 units/case. UPC 8-44334-00131-5.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2144-2012·2012-08-15
Smith & Nephew Dyonics Electroblade Resector Recalled for Labeling Error
Smith & Nephew is recalling Dyonics Electroblade Resectors labeled with an incorrect 48-month expiry date instead of 36 months.
Product
Smith & Nephew Dyonics Electroblade Resector, 4.5mm Full Radius Blade, BONECUTTER Part Number: 72202213 Product Usage: The Dyonics Electroblade Resector is indicated for use in arthroscopic surgical procedures of large and small articular cavities. The Dyonics Electroblade R
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2154-2012·2012-08-15
Greiner Bio-One Recalls Coagulation Blood Collection Tubes Due to Concentration Error
Greiner Bio-One is recalling specific lots of 3mL coagulation blood collection tubes because a lower citrate concentration may cause falsely low test results.
Product
3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North America Inc., 4238 Capital Drive, Monroe, NC 28110. Intended Use: Venous blood collection tubes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2161-2012·2012-08-15
Straumann Dental Implant Screw Recall Due to Incorrect Component
Straumann USA is recalling 14 dental implant sets because the included screw was not the correct Narrow CrossFit model.
Product
Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous dental implant Article Number: 027.2650 Product Usage: Dental implants are intended for surgical placement in maxillary and/or mandibular arches to provide support for prosthetic restorations using a
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2160-2012·2012-08-15
Afassco Multi-Colored Finger Cots Recalled for Missing Latex Warning Label
Afassco Inc. is voluntarily correcting a field issue for multi-colored finger cots that lack the required natural rubber latex warning label.
Product
The finger cots are made out of natural rubber. They are disposable products used to cover a fingertip bandage when working with liquids and are intended to keep the fingertip bandage dry. Cots are packed in clear plastic boxes, with 60 cots in a box They are disposable produ
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2147-2012·2012-08-15
ConMed Linvatec Recalls CrossFT Punch Due to Incorrect Etching
ConMed Linvatec is recalling 2 units of the CrossFT Punch (Lot #156920) because the device may have incorrect item numbers and depth lines.
Product
CrossFT Punch, Product Number PFT-45M. Manufacturer: CONMED LINVATEC. The intended use is to create a hole to facilitate insertion of the CrossFT suture anchor into bone.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2180-2012·2012-08-15
AngioDynamics Recalls Soft-Vu Angiographic Catheters Due to Mislabeled Pouches
AngioDynamics is recalling one lot of Soft-Vu angiographic catheters because a pouch inside the box may be mislabeled.
Product
AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. --- Size: 5F; Length: 100cm; designed to accept guidewire: .035 in. --- Catalog No. [REF]: 10734201. Packaged in boxes of 5 catheters each, with manufacturer listed as AngioDynamics, Inc., Queensbury, NY USA.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2145-2012·2012-08-15
Smith & Nephew Dyonics Bonecutter Recalled for Incorrect Expiry Labeling
Smith & Nephew is recalling 108 units of the 5.5 mm Dyonics Bonecutter because the devices are labeled with a 48-month expiry instead of the validated 36-month period.
Product
Smith & Nephew 5.5 mm Dyonics Bonecutter ,Electroblade Full Radius Part Number: 7205962 Product Usage: The Dyonics Electroblade Resector is indicated for use in arthroscopic surgical procedures of large and small articular cavities. The Dyonics Electroblade Resector is eff
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2146-2012·2012-08-15
Encore Medical Recalls Mislabelled 6.5 mm Cancellous Bone Screws
Encore Medical is recalling 18 bone screws because the package label incorrectly states the size is 30mm, while the actual screw dimension is 25mm.
Product
djo surgical Screw 6.5 mm, Sz 25mm, low profile. Product is intended for the fixation of the acetabular shell or fracture repair
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1929-2012·2012-08-15
Great American Seafood Cooked Shrimp Meat Recalled for Undeclared Dyes
Southwind Foods is recalling cooked shrimp meat because it contains undeclared red #40 and yellow #6 colors.
Product
Great American Seafood Imports Co. Cooked Shrimp Meat. Size: 300/500 count per pound in 2-lb (item #06834) and 5-lb (Item #07756) packages.
Category
Food
Distribution
Distributed nationwide