The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (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.

5101–5125 of 9610

  • ModerateFDA (Devices)·Z-0715-2017·2016-12-14

    Angiodynamics Recalls PICC Catheters Due to Stylet Diameter Labeling Error

    Angiodynamics is recalling PICC catheters because the stylet diameter may be larger than stated on the label.

    Product
    Peripherally Inserted Central Catheters (PICC), UPN H965750191, Catalog # 75-019 The Maximal Barrier Nursing Kits are Tandem Pack Convenience Kits packaged with a NMI PICC and accessories. The BioFlo PICC with ENDEXO Technology and BioFlo PICC with ENDEXO and PASV Valve Techn
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0711-2017·2016-12-14

    Encore Medical Recalls Mislabeled Empowr Knee Baseplate Implants

    Encore Medical is recalling seven Empowr Knee System baseplates that were mislabeled as size 6 but are actually size 4.

    Product
    Empowr Knee System Product Usage: Non-porous proximal tibial baseplate implants, utilized in either posterior cruciate ligament (PCL) retaining or PCL substituting total knee arthroplasty procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0606-2017·2016-12-14

    Safecor Vitamin B-1 Tablets Recalled for Incorrect Ingredient Labeling

    Safecor Health is recalling Vitamin B-1 tablets because the boxes are labeled with the wrong chemical form of thiamine.

    Product
    Safecor Vitamin B-1 (THIAMINE) 100 mg tablets NDC: 48433-0108-01 Distributed by: SAFECOR HEALTH, 317 NEW BOSTON STREET, WOBURN, MA
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0722-2017·2016-12-14

    OraSure Barbiturate Micro-Plate EIA Recalled for Shipping Error

    OraSure Technologies is recalling four kits of Barbiturates Intercept Micro-Plate EIA because cocaine metabolite microplates were shipped instead.

    Product
    Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay, barbiturate) Product is intended for use by clinical laboratories in the qualitative determination of barbiturates in oral fluids.
    Category
    Medical Device
    Distribution
    2 states
  • SevereUSDA FSIS·116-2016·2016-12-08

    Taylor Farms Recalls Meatloaf Products Due to Misbranding and Undeclared Allergens

    Taylor Farms Northwest is recalling approximately 79 pounds of meatloaf products due to misbranding and undeclared allergens, including milk, fish, beef, and pork.

    Product
    Taylor Farms Northwest LLC — Taylor Farms Northwest, LLC Recalls Meatloaf Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·16V882000·2016-12-08

    Starcraft RV Recalls 2017 Mini Trailers With Incorrect Tire Labels

    Starcraft RV is recalling 125 model year 2017 mini trailers because federal labels may list incorrect tire and rim sizes, potentially leading to unsafe replacements.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AUTUMN RIDGE, COMET MINI, LAUNCH, SATELLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0674-2017·2016-12-07

    Terumo BCT Recalls Adiprep Adipose Transfer System Due to Labeling Error

    Terumo BCT is voluntarily recalling 660 units of the Adiprep Adipose Transfer System because incorrect labeling could cause operator confusion.

    Product
    Adiprep Adipose Transfer System. Product Codes: 51431; 51432; 51433; 514001-347.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0658-2017·2016-12-07

    ConforMIS iTotal Knee Replacement System Recalled for Incorrect Serial Number Labeling

    ConforMIS is recalling two sterile iTotal Knee Replacement Systems distributed to Colorado and Nevada due to incorrect serial numbers on the F4 A/P cut guide iJig.

    Product
    ConforMIS iTotal Cruciate Retaining (CR) Knee Replacement System, Sterile Catalog Number: TCR-111-1111. Intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot be solely addressed by the use of a prosthetic device.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0681-2017·2016-12-07

    Synthes 0.76 mm Drill Bit Recalled for Incorrect Labeling

    Synthes (USA) Products LLC is recalling 84 units of 0.76 mm Drill Bits that may be incorrectly labeled and actually contain 1.1 mm drill bits.

    Product
    Synthes 0.76 mm Drill Bit/Stryker J-Latch/with 5mm Stop/44.5 mm Non-Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0682-2017·2016-12-07

    Sorin Group Recalls Stöckert Heater Cooler System 3T for Disinfection Review

    Sorin Group USA is recalling Stöckert Heater Cooler System 3T units to ensure strict adherence to disinfection and monitoring instructions.

    Product
    ST¿CKERT HeaterCooler System 3T; Item Number 160281, HeaterCooler 3T, 240V/60Hz; Item Number 160282, HeaterCooler 3T, 208V/60Hz; Item Number 160285, HeaterCooler 3T, 120V/ 60Hz The Heater Cooler 3T is used with a St¿ckert S3 heart lung machine and / or any other heart
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V866000·2016-12-02

    Forest River Recalls 2017 Puma Trailers for Incorrect Federal Tire Placards

    Forest River is recalling 2017 Puma trailers because incorrect Federal placards list wrong tire and rim information, which could lead to under-inflation and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0481-2017·2016-11-30

    Café Valley Recalls Banana Nut Mini Muffins for Undeclared Walnuts

    Café Valley Inc. is voluntarily recalling 1,170 cases of Banana Nut mini muffins mislabeled as Lemon Poppy Seed because they may contain undeclared walnuts.

    Product
    12ct Banana Nut mini muffins labeled as 12ct Lemon poppy seed mini muffins; Date code 160803 ink jet printed on top near the label.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0523-2017·2016-11-30

    CSM Bakery Products Recalls White Cake Mix for Undeclared Peanut

    CSM Bakery Products is recalling Brill White Crm Cake Mix because it contains undeclared peanut protein. The product was distributed across 19 states and two territories.

    Product
    Brill White Crm Cake Mix, 50#
    Category
    Food
    Distribution
    19 states
  • ModerateFDA (Food)·F-0494-2017·2016-11-30

    Infiniti Creations Recalls HCG Diet Plan Drops Due to Misbranding

    Infiniti Creations, LLC is voluntarily recalling HCG Diet Plan drops due to misbranding and potential undeclared HCG content.

    Product
    Official HCG Diet Plan. 1oz, 2oz & 4oz HCG Drops. Amber Plastic and Glass.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0499-2017·2016-11-30

    Infiniti Creations Recalls Amino Complex Formula Due to Misbranding

    Infiniti Creations, LLC is voluntarily recalling Amino Complex Formula HCG Drops due to misbranding and potential undeclared HCG.

    Product
    Amino Complex Formula. 2oz HCG Drops. Blue Glass.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0483-2017·2016-11-30

    Infiniti Creations Recalls HCG Plus Drops Due to Misbranding

    Infiniti Creations, LLC is voluntarily recalling HCG Plus drops due to misbranding and potential undeclared HCG content.

    Product
    HCG Plus. 2oz HCG Drops. Blue Glass
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0628-2017·2016-11-30

    DePuy Spine Recalls SKYLINE Anterior Cervical Plate Screws

    DePuy Spine is recalling 9 units of SKYLINE Variable Oversized Screws because they may have been packaged with Constrained Ti screws.

    Product
    DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE OVERSIZED SCREW 4.5 x 18mm Item Code: 186854018 The SKYLINE¿ Anterior Cervical Plate System is indicated for stabilization from C2 to C7 for degenerative disc disease (DDD) (defined as back pain of discogenic origin
    Category
    Medical Device
    Distribution
    15 states