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.

2326–2350 of 9607

  • ModerateFDA (Devices)·Z-0912-2020·2020-02-05

    GIBSON Healthcare Membrane Extended Recalled for Incorrect Instructions for Use

    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, 30mm x 40mm, Reference Number 5303-342 - 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-0909-2020·2020-02-05

    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, 30mm x 40mm, Reference Number 5303-299 - 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 (Devices)·Z-0910-2020·2020-02-05

    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, 15mm x 20mm, Reference Number 5303-306 - - 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; locali
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0876-2020·2020-02-05

    GE Healthcare Recalls SIGNA Pioneer MRI Systems Due to Date Errors

    GE Healthcare is recalling 62 SIGNA Pioneer MRI systems because an installation issue may cause incorrect dates on medical images.

    Product
    SIGNA Pioneer 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 (Food)·F-0528-2020·2020-01-29

    Pike Place Chowder Recalled for Gluten Free Labeling Error

    Northwest Gourmet Food Products Inc. is recalling Pike Place Chowder New England Clam Chowder because the outer packaging claims 'Gluten Free' while the inner pouch declares wheat.

    Product
    New England Clam Chowder, Pike Place Chowder brand, item #89200, distributed By PPC Trading Co. M. BOX #262 4580 Klahanie Drive SE Issaquah WA 98029. There are 12/16 oz. retail packages per master case. Retail package net wt. 16 oz. UPC 8 56112 00402 9. The 16 oz. inner i
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0801-2020·2020-01-29

    Hikma Recalls Methylprednisolone Sodium Succinate Injection Due to Labeling Error

    Hikma Pharmaceuticals is recalling 4,840 vials of Methylprednisolone Sodium Succinate Injection because the label incorrectly instructs healthcare professionals to reconstitute the product with 16 mL instead of 8 mL.

    Product
    METHYLPREDNISOLONE SODIUM SUCCINATE — METHYLPREDNISOLONE SODIUM SUCCINATE (METHYLPREDNISOLONE SODIUM SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0844-2020·2020-01-29

    Arrow Arterial Catherization Kit Recalled for Incorrect MR Labeling

    Arrow International is recalling 80 kits due to a lidstock label error that displays an MR Conditional symbol instead of MR Unsafe.

    Product
    Arrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018" (0.46 mm) dia. Spring-Wire Guide Product Code: ASK-04020-PMC The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial ci
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0657-2020·2020-01-22

    FDA Recalls Panther Platinum 30000 Capsules for Unapproved Tadalfil Content

    Motto International Corp is recalling Panther Platinum 30000 Capsules because FDA analysis found the product contains tadalfil and was marketed without an approved NDA or ANDA.

    Product
    Panther Platinum 30000 Capsules, in green, black background with white, red text in hologram paper packaging, packaged in 2, 4, and 10 count blister cards, Motto International, Dallas, TX
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0656-2020·2020-01-22

    FDA Recalls Rhino 7 Platinum 30000 Capsules for Unapproved Tadafila Content

    Motto International Corp is recalling Rhino 7 Platinum 30000 Capsules because FDA analysis found the product contains tadalafil, an unapproved active ingredient.

    Product
    Rhino 7 Platinum 30000 Capsules, in blue,orange,black background with red,white,blue,gray text in hologram paper packaging, packaged in 2, 4, and 10 count blister cards, Motto International, Dallas, TX
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-0543-2020·2020-01-22

    Wegmans Recalls Crab Stuffed Portobella for Undeclared Soy

    Wegmans is recalling Crab Stuffed Portobella mushrooms due to undeclared soy. The product was sold in seven states.

    Product
    Crab Stuffed Portobella; Wegmans Ready to Cook Portobella Mushroom with Crab Stuffing, Sold by the lb; Unit size varies; Oven ready tray; Package size varies; Keep Refrigerated
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0536-2020·2020-01-22

    Wegmans Recalls Ready-to-Cook Crab Stuffing for Undeclared Soy

    Wegmans is recalling Ready to Cook Crab Stuffing sold in seven states because the product contains undeclared soy.

    Product
    Crab Stuffing; Wegmans Ready to Cook Crab Stuffing, Sold by the lb; Unit size varies; Oven ready tray; package size varies, Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0500-2020·2020-01-22

    Sanity Chocolate Recalls Dark with Browned Ghee for Undeclared Milk

    Sanity Chocolate is recalling approximately 60 bars of Dark with Browned Ghee chocolate because the label declares ghee but fails to declare milk.

    Product
    Dark with Browned Ghee is wrapped in a foil and jacketed with black paper. There is a white sticker on the front that says Sanity Chocolate. On the back label there is the batch name listed above, address listed above and ingredient list. Average net weight is 0.75 oz. There i
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0552-2020·2020-01-22

    Wegmans Recalls Lobster Stuffed Tilapia for Undeclared Soy

    Wegmans is recalling Lobster Stuffed Tilapia because the product contains undeclared soy. Consumers with soy allergies should not eat the product.

    Product
    Lobster Stuffed Tilapia; Wegmans Ready to Cook Lobster Stuffed Tilapia, 7 oz; Unit size 7oz; Oven Ready Tray; Package size 7oz; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0560-2020·2020-01-22

    Tobago Keys Seafood and Grilling Sauces Recalled for Undeclared Fish Allergen

    Endorphin Farms, Inc. is recalling Tobago Keys brand sauces due to mislabeling that resulted in an undeclared fish allergen.

    Product
    Tobago Keys brand Coral Ridge Seafood Dipping Sauce 12 FL.OZ. (355 ml) and Peruvian Gold Grilling Sauce 12 FL.OZ (355 ml)
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0549-2020·2020-01-22

    Wegmans Lobster Stuffed Portabella Recalled for Undeclared Soy

    Wegmans is recalling Lobster Stuffed Portabella mushrooms because they contain undeclared soy. Consumers with soy allergies should not eat the product.

    Product
    Lobster Stuffed Portabella; Wegmans Ready to Cook Lobster Portabella Mushroom, Sold by the lb; Unit size varies; Oven ready tray; Package size varies; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0526-2020·2020-01-22

    Royal Farms Barbecue Dipping Sauce Recalled for Undeclared Soy Allergen

    Sauer Brands is recalling Royal Farms Barbecue Dipping Sauce because the label fails to declare the presence of soy lecithin, a major allergen.

    Product
    Royal Farms Barbecue Dipping Sauce, Net Wt. 1.5 OZ Distributed by Royal Farms, Baltimore MD packaged in plastic cups, 228 cups to a case.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0537-2020·2020-01-22

    Wegmans Recalls Crab Stuffed Hot Peppers Due to Undeclared Soy

    Wegmans is recalling Ready to Cook Crab Stuffed Hot Peppers because they contain undeclared soy. The product was sold in seven states.

    Product
    Crab Stuffed Hot Peppers; Wegmans Ready to Cook Crab Stuffed Hot Peppers, Sold by the lb; Unit size varies; Oven ready tray; Package size varies; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0542-2020·2020-01-22

    Wegmans Recalls Salmon with Crab Stuffing Due to Undeclared Soy

    Wegmans is recalling Salmon with Crab Stuffing because the product contains undeclared soy. Consumers should not eat the product and should return it to the store.

    Product
    Salmon with Crab Stuffing; Wegmans Salmon Topped with Crab Stuffing; 8 oz; Oven ready tray; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0812-2020·2020-01-22

    Microbiologics Gram-Positive Blood Culture Control Panel Recall for Hydration Fluid Change

    Microbiologics Inc is recalling 810 units of the Gram-Positive Blood Culture Control Panel because the recommended hydration fluid has changed to sterile DI water or pH 7.2 phosphate buffer.

    Product
    Microbiologics QC Sets and Panels, Gram-Positive Blood Culture Control Panel (Inactivated Pellet), Catalog # 8180 Used in test systems to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation.
    Category
    Medical Device
    Distribution
    Distributed nationwide