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.

8801–8825 of 9622

ModerateFDA (Drugs)·D-250-2013·2013-04-24
Precision Dose Recalls Children's Acetaminophen Due to Misleading Labeling
Precision Dose Inc. is recalling Children's Acetaminophen Oral Suspension because the label is misleading. The product contains an adult dose of acetaminophen despite the name.
Product
Children's Acetaminophen Oral Suspension, 650 mg/20.3 mL unit dose cup (NDC 68094-650-59), packaged in 30-count cups per shipper case (NDC 68094-650-62), Pkg. By: Precision Dose, Inc., S. Beloit, IL 61080.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1120-2013·2013-04-24
Siemens ADVIA Centaur Vitamin D Assay Recalled for Negative Bias
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Vitamin D Assay kits due to negative bias in patient samples.
Product
ADVIA Centaur Vitamin D Assay (500 tests); Reference Number:10631021. For use in the quantitative determination of Vit D.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1140-2013·2013-04-24
Nipro TRUEtrack Blood Glucose Monitor Kits Recalled for Labeling Error
Nipro Diagnostics is recalling 1,627 TRUEtrack monitor kits because the outer boxes state an incorrect storage temperature range for the test strips.
Product
Duane Reade TRUEtrack monitor kit, UPC# 6 39194 01679 7 Part # A4006-81 The TRUEtrack Blood Glucose System is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm. The System is intended to be used to assist the patient and h
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1318-2013·2013-04-24
Cypress Grove Humboldt Fog Goat Cheese Recalled for Incorrect Ingredient Labeling
DPI Specialty Foods is recalling Cypress Grove Humboldt Fog Goat Cheese because it was labeled as containing cultured raw cow's milk instead of pasteurized goat milk.
Product
Humboldt Fog (brand) Cypress Grove Chevre, Aged Goat Milk Cheese. Packaged in 7oz (random weight) and 5 oz (random weight). Cypress Grove Chevre # 213146 7oz (random weight) Cypress Grove Chevre # 35363 5oz (random weight) Products are random (various) weight.
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-1020-2013·2013-04-24
DeGotzen XGenus Dental X-ray Units Recalled for Labeling Defects
DeGotzen is recalling 159 XGenus dental X-ray units because method samples failed labeling and certification requirements.
Product
DeGotzen XRay unit XGenus Dental X-ray unit.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1132-2013·2013-04-24
Smith & Nephew Recalls Trigen Bone Screws Due to Incorrect Coating
Smith & Nephew is recalling 23 units of 4.5 mm Trigen bone screws that were incorrectly anodized with a gold coating instead of gray.
Product
TRIGEN (TM) L-P SCREW, 4.5 MM X 37.5 MM, TI-6AL-4V, QTY: (1), STERILE R, REF 71645437, Smith & Nephew, Inc. Memphis, TN 38116 USA orthopedic surgery
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·13V150000·2013-04-19
Prevost Recalls Coach Buses Due to Incorrect Emergency Window Decals
Prevost is recalling specific coach buses because emergency window decals omit a required step to open the windows, potentially increasing injury risk in a crash.
Product
PREVOST — PREVOST XLII-45 ENTERTAINER, XLII-45, H3-45 VIP, X3-45 VIP
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1058-2013·2013-04-17
Respironics Infant Masks Recalled Due to Incorrect Size Labeling
Engineered Medical Systems is recalling Respironics SealFlex Single Port Ribbed Masks labeled as Infant but actually Neonatal size.
Product
Respironics SealFlex Single Port Ribbed Mask (Infant). For general use in respiratory and anesthesia applications as a conduit for various gases to resuscitate or to enhance breathing abilities of the patient. .
Category
Medical Device
Distribution
5 states
HighFDA (Food)·F-1301-2013·2013-04-17
Sunchang Ssamjang Sesame and Garlic Bean Paste Recalled for Peanut Mislabeling
Daesang America is recalling Sunchang Ssamjang bean paste because the English label omits peanut powder, a major allergen listed in Korean.
Product
Sunchang Ssamjang Sesame and Garlic Seasoned Bean Paste 500 g - Net Wt. 17.64 oz., UPC Code 880152435671 Distributed by: Daesang America, Inc. Hackensack, NJ 07601 TEL: (201) 488-4010 Product of Korea
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1307-2013·2013-04-17
Mikesell's Honey Barbecue Potato Chips Recalled for Gluten Free Mislabeling
Mike-Sells Potato Chip Co is recalling Honey Barbecue flavored potato chips labeled as 'Gluten Free' due to mislabeling complaints.
Product
Mikesell's Honey Barbecue TOMATO AND SPICES WITH A HINT OF SWEET FLAVORED POTATO CHIPS Gluten Free 1 oz., 2 oz., 6 oz., 10 oz., 16 oz. MIKESELL'S SNACK FOOD CO. P.O. BOX 115 DAYTON, OH 45404.
Category
Food
Distribution
4 states
HighFDA (Food)·F-1308-2013·2013-04-17
Giant Eagle Cookies Recalled for Undeclared Soy Allergen
Giant Eagle is recalling Lotsa Chocolate Chip Cookies because the labels fail to declare soy lecithin, a major allergen present in the product.
Product
Giant Eagle Lotsa Chocolate Chip Cookies
Category
Food
Distribution
4 states
HighFDA (Food)·F-1295-2013·2013-04-17
NatureBox Umami Almonds Recalled for Undeclared Wheat Allergen
NatureBox is recalling 802 units of Umami Almonds because the product may contain wheat, which is not listed in the ingredient statement.
Product
NatureBox brand Umami Almonds packed in branded stand-up pouches (whole tamari flavored almonds), Net wt. 4.3 oz. No UPC Codes on the product, Product is processed and packaged by NatureBox, San Carlos, CA; NOTE: Product label DOES declare that it is "Packed in a facility
Category
Food
Distribution
0 states
ModerateFDA (Devices)·Z-1084-2013·2013-04-17
Ormco Recalls Bracket Buccal Tubes Due to Packaging Error
Ormco is voluntarily recalling one lot of Bracket Buccal Tubes because the packaging incorrectly identifies the product offset, which may cause unintended tooth rotation.
Product
Bracket Buccal Tube U7L DB/UL22 Roth MT HK 0/-14/0 Product Usage: Bracket Buccal Tubes are intended to hold in orthodontic wires used to move teeth during orthodontic treatment
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1092-2013·2013-04-17
Lighthouse For The Blind Recalls First Aid Kits Due to Sterility Labeling Error
Lighthouse For The Blind is recalling First Aid Type IV Belt Type kits because the iodine ampule labels incorrectly imply the entire package is sterile.
Product
LHB, First Aid Type IV Belt Type, NSN #6545-01-010-7754. Kit number: 114016. First Aid Kit.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1090-2013·2013-04-17
Lighthouse For The Blind Recalls First Aid Kits Due to Sterility Labeling Error
Lighthouse For The Blind is recalling 41,595 First Aid Type III kits because the iodine ampule labels incorrectly imply the entire package is sterile, rather than just the applicator.
Product
LHB, First Aid Type III, NSN # 6545-00-656-1094, Kit number: 2114011. First Aid Kit.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1089-2013·2013-04-17
Lighthouse For The Blind Recalls First Aid Kits Due to Sterility Labeling Error
Lighthouse For The Blind is recalling 1,034 First Aid Kits because the iodine ampule labels incorrectly imply the entire package is sterile, when only the applicator is sterile.
Product
LHB, Perishable Items Pack Type I , Kit Number: 2114002-100. First Aid Kit.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1087-2013·2013-04-17
Lighthouse For The Blind Recalls Antiseptic Kits Due to Sterility Labeling Error
Lighthouse For The Blind is recalling 2,815 antiseptic kits because the iodine ampule labels incorrectly imply the entire package is sterile, rather than just the applicator.
Product
LHB, Antiseptic Kit, Povidone Swab, Gauze Pads, and non-stick pads. Kit Number: 2113305. First Aid Kit.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1093-2013·2013-04-17
Lighthouse For The Blind Recalls First Aid Kits With Misleading Sterility Labels
Lighthouse For The Blind is recalling 425 First Aid Kits because the iodine ampule labels incorrectly imply the entire package is sterile, when only the applicator is sterile.
Product
LHB, Perishable Items Pack Type IV. Kit number: 2114016-100. First Aid Kit.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1086-2013·2013-04-17
Lighthouse For The Blind Recalls First Aid Kits Due to Sterility Labeling
Lighthouse For The Blind is recalling 635 Type I First Aid Kits because the iodine ampule labeling incorrectly implies the entire package is sterile.
Product
LHB, Type I First Aid Kit Perishable, Non-Aspirin 4/pg, Aspirin 4/pg and Povidone Iodine, antiseptic towelette. Kit Number: 2113110. First Aid Kit.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1088-2013·2013-04-17
Lighthouse For The Blind Recalls First Aid Kits Due to Sterility Labeling
Lighthouse For The Blind is recalling 56,133 First Aid Type I Individual Kits because the iodine ampule labels incorrectly imply the entire package is sterile.
Product
LHB, First Aid Type I Individual Kit, NSN: 6545-00-656-1092, antiseptics, Kit number: 2114002. First Aid Kit.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1091-2013·2013-04-17
Lighthouse For The Blind Recalls First Aid Kits Due to Sterility Labeling
Lighthouse For The Blind is recalling 227 First Aid Kits because the iodine ampule labeling incorrectly implies the entire package is sterile.
Product
LHB, Perishable Item Pack Type III. Kit number: 2114011-100. First Aid Kit.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1056-2013·2013-04-10
BD Vacutainer Urinalysis Transfer Straw Kit Recalled for Mislabeling
Becton Dickinson is recalling BD Vacutainer Urinalysis Transfer Straw Kits due to incorrect polybag labeling that may cause users to mistake the tube for a culture and sensitivity tube.
Product
BD Vacutainer C&S Transfer Straw Kit C&S Preservative Plus Urine Tube. 4.0 ml, 13 X 75 mm STERILE REF 364953. Becton Dickinson & Company, Franklin Lakes, NJ USA, The kit consists of a transfer straw and urinalysis tube intended for UA chemistry urine testing.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1057-2013·2013-04-10
Arrow Berman Angiographic Catheter Recall Due to Outdated Contrast Medium Labeling
Arrow International is recalling Berman Angiographic Catheters because the instructions reference a discontinued contrast medium. The firm is updating the labeling.
Product
Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse Berman Angiographic Balloon Catheter. The Arrow Berman(TM) Angiographic Catheter is indicated for use in right heart catheterization for cardiac angiography, and measurement of the right heart and pulmonar
Category
Medical Device
Distribution
50 states
ModerateFDA (Devices)·Z-1053-2013·2013-04-10
Cooper Surgical Recalls LEEP RediKit Due to Incorrect Anesthetic Labeling
Cooper Surgical is recalling LEEP RediKit products because the tray lid label incorrectly lists Xylocaine, while the kit actually contains Polocaine.
Product
LEEP REDIKIT Product No. 6060 In a Loop Electrosurgical Excision Procedure, a thin, low-voltage electrified wire loop is used to cut out abnormal cervical tissue. The cartridges of Polocaine and Xylocaine with Epinephrine contained in the LEEP RediKit are local anaestheti
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-240-2013·2013-04-10
Ferring Recalls TEV-TROPIN Due to Needle-Free Head Labeling Error
Ferring Pharmaceuticals is recalling 126 injectors of TEV-TROPIN because the cartons are labeled for Needle-Free Head B but contain Needle-Free Head A.
Product
TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Prescription Only. Distributed By: TEVA Biologics & Specialty Products Division of Teva Pharmaceuticals USA, Sellersville, PA 18960 Manufactured in Israel.
Category
Drug
Distribution
Distributed nationwide