The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) are Severe.

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.

2301–2325 of 9607

  • HighFDA (Drugs)·D-0814-2020·2020-02-05

    Sildenafil 200 mg Troche Recall for Labeling and Expiry Issues

    Sildenafil 200 mg Troche is recalled for incorrect labeling and being compounded with expired components. Consumers in Texas should check their bottles and contact the manufacturer for instructions.

    Product
    Sildenafil 200 mg Troche (Clinic)
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-0917-2020·2020-02-05

    Bard Conquest 40 PTA Dilation Catheter Recalled for Packaging Error

    Bard Peripheral Vascular Inc. is recalling 286 units of Conquest 40 PTA Dilation Catheters because packaging incorrectly listed the balloon size, posing a risk of vessel injury.

    Product
    Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire .035"; Recommended Introducer 6F; Nominal Pressure 8atm, Rated Burst Pressure 40atm; Syringe inflation 1cc; UDI: (01)00801741060533(17)220228(10)REDQ3444
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Devices)·Z-0913-2020·2020-02-05

    Beckman Coulter Recalls iChemVELOCITY Urine Chemistry Systems Due to Data Errors

    Beckman Coulter is recalling iChemVELOCITY Urine Chemistry Systems because they may report duplicate specimen IDs with conflicting patient data and results.

    Product
    iChemVELOCITY, Urine Chemistry System, Catalog numbers: 700-7176-001, 700-7177-001, B75502 - Product Usage: used to automate the urine chemistry analysis profile using iChem¿ VELOCITY Urine Chemistry Strips.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0820-2020·2020-02-05

    MPRX Recalls Testosterone Topical Cream 4% Due to Expired Components

    MPRX, Inc. dba Medical Park Pharmacy is recalling Testosterone Topical Cream 4% because it was compounded using expired components and has incorrect or missing lot and expiration dates.

    Product
    Testosterone Topical Cream 4%
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0813-2020·2020-02-05

    Progesterone E4M SR 100 mg capsules recalled for expired components

    MPRX, Inc. is recalling specific lots of compounded Progesterone E4M SR 100 mg capsules because they were made with expired components and have incorrect labeling.

    Product
    Progesterone E4M SR 100 mg capsules
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0911-2020·2020-02-05

    Collagen Matrix Recalls GIBSON Membrane Due to Incorrect Instructions

    Collagen Matrix Inc is recalling 192 units of GIBSON Healthcare Membrane Extended because they may have been packaged with incorrect Instructions for Use.

    Product
    GIBSON Healthcare Membrane Extended, 20mm x 30mm, Reference Number 5303-324 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localize
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0873-2020·2020-02-05

    Exactech Equinoxe Humeral Stem Recalled for Incorrect Label Translation

    Exactech is recalling Equinoxe humeral stems because outer labels incorrectly described the standard-length implants as 'long' in non-English translations.

    Product
    Exactech equinoxe PLATFORM FRACTURE, HUMERAL STEM, CEMENTED, Right, 10.5mm, REF 304-22-11 - Product Usage: The Equinoxe Shoulder System is indicated for use and in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint work total or hemi-
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0562-2020·2020-02-05

    Ground Ginger Recalled for Missing Sulfite Labeling in California

    H.L. Foodservice is recalling 620 lbs of ground ginger sold in California because the packages do not identify the addition of sulfites.

    Product
    Ground Ginger in clear plastic bags; Sold in 1 lb. and 5 lb. bags Country of Origin: India 1 lb. UPC: 0 00000 94641 4 5 lb. UPC: 0 00000 94642 1 Pack by: H.L. FoodserviceInc.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0809-2020·2020-02-05

    MPRX Recalls Magic Bullet Supplement Due to Expired Components

    MPRX, Inc. is recalling Magic Bullet Supplement bottles compounded with expired components and incorrect labeling. The recall affects products distributed in Texas.

    Product
    Magic Bullet Supplement
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0872-2020·2020-02-05

    Exactech Equinoxe Humeral Stem Recalled for Incorrect Label Translation

    Exactech is recalling 2,910 Equinoxe humeral stems because outer labels incorrectly described the standard-length implants as 'long' in non-English translations.

    Product
    Exactech equinoxe PLATFORM FRACTURE, HUMERAL STEM, CEMENTED, Right, 6.5mm, REF 304-22-07 - Product Usage: The Equinoxe Shoulder System is indicated for use and in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint work total or hemi- a
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0874-2020·2020-02-05

    GE Healthcare Recalls SIGNA Premier MRI Systems Due to Date Errors

    GE Healthcare is recalling 62 SIGNA Premier MRI systems because a potential installation issue could cause incorrect dates to be recorded on medical images.

    Product
    SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0884-2020·2020-02-05

    Brasseler USA Recalls Mislabelled Steinmann Pins for Bone Fracture Fixation

    Brasseler USA is recalling 103 tubes of Steinmann Pins that were incorrectly labeled as threaded pins instead of smooth pins.

    Product
    Brasseler USA KM169-39-76 Steinmann Pin Single Diamond Smooth, Diameter 2.8 mm, Length 228 mm Product Usage: A Steinmann Pin is used for internal fixation of large bone fractures.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0908-2020·2020-02-05

    GIBSON Healthcare Membrane Recalled for Incorrect Instructions for Use

    Collagen Matrix Inc is recalling GIBSON Healthcare Membrane 6-9 units because they may have been packaged with incorrect Instructions for Use.

    Product
    GIBSON Healthcare Membrane 6-9, 20mm x 30mm, Reference Number 5303-235 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized rid
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0812-2020·2020-02-05

    Progesterone 50 mg Capsules Recalled for Expired Components

    MPRX, Inc. is recalling Progesterone 50 mg capsules compounded with expired components due to incorrect or missing lot and expiration dates.

    Product
    Progesterone 50 mg capsules
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0817-2020·2020-02-05

    Medical Park Pharmacy Recalls T3/T4 SR Capsules Due to Labeling Errors

    MPRX, Inc. dba Medical Park Pharmacy is recalling T3/T4 SR 9 mcg/38 mcg capsules due to incorrect or missing lot and expiration dates and the use of expired components.

    Product
    T3/T4 SR 9 mcg/38 mcg capsule
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0810-2020·2020-02-05

    Medical Park Pharmacy Recalls Naltrexone Capsules Due to Labeling Errors

    MPRX, Inc. dba Medical Park Pharmacy is recalling Naltrexone 4.5 mg capsules because they were compounded using expired components and have incorrect or missing lot and expiration dates.

    Product
    Naltrexone 4.5 mg capsule
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0808-2020·2020-02-05

    Medical Park Pharmacy Recalls Liothyronine Due to Expired Components

    MPRX, Inc. dba Medical Park Pharmacy is recalling Liothyronine (T3) 92.5 MCG compounded with expired components due to incorrect or missing lot and expiration dates.

    Product
    Liothyronine (T3) 92.5 MCG
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0875-2020·2020-02-05

    GE Healthcare Recalls SIGNA Architect MRI Systems Due to Date Errors

    GE Healthcare is recalling SIGNA Architect MRI systems because a potential installation issue may cause incorrect dates to be recorded on medical images.

    Product
    SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0907-2020·2020-02-05

    Collagen Matrix Recalls GIBSON Membrane Due to Incorrect Instructions

    Collagen Matrix Inc is recalling 192 units of GIBSON Healthcare Membrane 6-9 because they may have been packaged with incorrect Instructions for Use.

    Product
    GIBSON Healthcare Membrane 6-9, 15mm x 20mm, Reference Number 5303-226 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized rid
    Category
    Medical Device
    Distribution
    Distributed nationwide