The Recall Desk

Hazard

Mislabeling recalls

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

What the numbers show

Total
395
Critical
20
Severe
45
Most recent
2026-07-22

Of the 395 mislabeling recalls we have scored against our rubric, 20 (5%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 45 (11%) 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 mislabeling 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.

76–100 of 395

  • HighFDA (Food)·H-0010-2026·2025-10-08

    Diet green tea bottles recalled after being filled with sugared citrus tea

    PepsiCo is recalling 2,854 cases of Lipton tea because bottles labeled Diet Green Tea Mixed Berry with 0g sugar contain Green Tea Citrus with 25g sugar.

    Product
    Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as 12pk. Outer case label reads as , "*** Lipton Green Tea Citrus (25g sugar)***" Individual bottle label reads as "*** Lipton Diet Green Tea Mixed Berry (0g sugar)***). Shelf stable.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·H-0008-2026·2025-10-08

    Raspberry peach jam cookies recalled for undeclared Red 3 and Blue 1

    Vanilla Cookies with Raspberry Peach Jam are being recalled because the colour additives Red 3 and Blue 1 are not declared on the label. The recall covers 172 cases.

    Product
    Vanilla Cookies with Raspberry Peach Jam
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2640-2025·2025-10-08

    Hip stems recalled over potential mix of two catalog numbers in packaging

    Howmedica Osteonics is recalling 55 Exeter V40 hip stems because packages labeled for one catalog number may contain the other size, and patient labels may also be affected.

    Product
    1. EXETER V40 STEM 44MM NO 2, Model/Catalog Number: 0580-1-442; 2. EXETER V40 STEM 37.5MM NO 0, Model/Catalog Number: 0580-1-352;
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·H-0028-2026·2025-10-01

    Macaroni and cheese cartons recalled nationwide for undeclared cashew allergen

    GOODLES is recalling 61,176 cartons of Here Comes Truffle creamy truffle flavored cheddar and shells because the product contains cashews that are not declared on the label.

    Product
    GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR AND SHELLS NET WT 6 OZ (170g) INGREDIENTS: GOODLES SHELLS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI, SPINACH, KALE, PUMPKIN, SWEET POTATO, SUNFLOWER SEED, CRANBERRY, CHLORELLA, MAIT
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Devices)·Z-2619-2025·2025-10-01

    Soft tissue anchors recalled after cartons packed with wrong device size

    Zimmer Biomet is recalling JuggerKnot Mini Soft Anchors after outer cartons labeled for the 1.0mm Mini product were found to contain 1.4mm Short devices instead.

    Product
    Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2532-2025·2025-09-17

    Introducer sheath systems recalled over pouch labels showing the wrong size

    Fortress Introducer Sheath Systems, 6F straight 45 cm, lot 800989, are recalled because units may carry a pouch label listing the reference number and UDI of the 4F version. 2,500 units are affected.

    Product
    Brand Name: Fortress Introducer Sheath System Product Name: Fortress Introducer Sheath System Model/Catalog Number: 386594 Product Description: Fortress Introducer Sheath System, 6F Straight 45cm:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2479-2025·2025-09-03

    Surgical kits recalled because Foley tray inserts carry incorrect product information

    Medline kits containing BD SureStep Foley Tray Systems are recalled because the trays include incorrect product information insert sheets. Four units were distributed, all from the LAVH MINOR SKU.

    Product
    Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTIC DYNJG001004A LAVH MINOR DYNJG901001B CRANIOTOMY DYNJ908819B KIT CRANIOTOMY (only units from SKU DYNJG001004A LAVH MINOR were distributed)
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·H-0504-2025·2025-08-27

    Zero sugar soda cans recalled because they contain full sugar product

    7up Zero Sugar Tropical Soda in 12 fl oz cans is recalled because the cans are labeled Zero Sugar but contain full sugar product. 1,954 cases are affected.

    Product
    7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up Tropical Flavored Soda, UPC (on can): 078000037975, UPC (on carton): 078000037982
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2344-2025·2025-08-27

    OtoLase starter kits recalled over potentially unsterilized product labeled as sterile

    OtoLase Starter Kits, UPN AC-2003748, batches 32644549 and 32769567, are recalled because finished product labeled as sterile may not have been sterilized. 13 units are affected.

    Product
    OtoLase Starter Kit; UPN: AC-2003748. Indicated for a variety of surgical uses including ablation, coagulation, incision, excision, and vaporization of soft tissue.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2345-2025·2025-08-27

    ELISA sample tip racks recalled over internal label misidentifying tip type

    Dynex Agility Sample Tips, model 67910 lot 863366, are recalled because the internal rack label reads reagent tip rack, causing the instrument to misidentify the tips and preventing their use. 237 units are affected.

    Product
    Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used with the Agility Automated ELISA system.
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·H-0465-2025·2025-08-20

    La Michoacana variety paletas list cream without declaring milk as source

    La Michoacana Minis Variety Paletas 12-count are being recalled because the label includes the ingredient cream but does not include milk as the source. 29,180 units are affected.

    Product
    La Michoacana Minis Variety Paletas 12-Count 16.5oz UPC: 7-67778-03042-3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2285-2025·2025-08-20

    Knee tibial insert catalog number 341-16-704 recalled for mislabeled size or side

    Enovis is recalling 18 EMPOWR 3D Knee tibial inserts, catalog number 341-16-704, lot 148T1057, because the implants carry incorrect size or side labeling.

    Product
    Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number: 341-16-704 Product Description: Enovis knee devices are intended for treatment of patients who are candidates for knee arthroplasty per the Indication for use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0459-2025·2025-08-20

    La Michoacana strawberry paletas list cream without declaring milk as source

    La Michoacana Strawberry Con Crema Single Serve Paletas are being recalled because the label includes the ingredient cream but does not include milk as the source. 62,864 units affected.

    Product
    La Michoacana Strawberry Con Crema Single Serve Paleta 3.75oz UPC: 7-67778-00002-0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0470-2025·2025-08-20

    Helados Mexico choco dipped paletas list cream without declaring milk

    Helados Mexico Choco Dipped Minis Variety Paletas 12-count are being recalled because the label includes the ingredient cream but does not include milk as the source. 70,044 units affected.

    Product
    Helados Mexico Choco Dipped Minis Variety Paletas 12-Count 18oz UPC: 6-82082-41215-7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2279-2025·2025-08-20

    Polyaxial screws in lot 8-4528 recalled over possible incorrect labeling

    PERLA TL MIS cannulated fenestrated polyaxial screws, model MPF-PS 65 40-S, lot 8-4528, are recalled because the screws may be incorrectly labeled. 16 units are affected.

    Product
    Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 65 40-S Software Version: Not Applicable Product Description: CANNULATED FENESTRATED POLYAXIAL SCREW Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0469-2025·2025-08-20

    Helados Mexico variety paletas list cream without declaring milk as source

    Helados Mexico Minis Variety Paletas 12-count are being recalled because the label includes the ingredient cream but does not include milk as the source. 42,488 units are affected.

    Product
    Helados Mexico Minis Variety Paletas 12-Count 18oz UPC:6-82082-61215-1
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2280-2025·2025-08-20

    Cannulated fenestrated polyaxial screws recalled because they may be incorrectly labeled

    PERLA TL MIS cannulated fenestrated polyaxial screws, model MPF-PS 55 45-S, lot 8-4266, are recalled because the screws may be incorrectly labeled.

    Product
    Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S Software Version: Not Applicable Product Description: CANNULATED FENESTRATED POLYAXIAL SCREW
    Category
    Medical Device
    Distribution
    Distributed nationwide