The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 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 589 (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.

8676–8700 of 9611

  • HighFDA (Devices)·Z-1406-2013·2013-06-05

    AngioDynamics Recalls VenaCure EVLT NeverTouch Procedure Kits Due to Sizing Error

    AngioDynamics is recalling VenaCure EVLT NeverTouch Procedure Kits because the packaged micro Introducer may be the wrong French size.

    Product
    AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following labeling: 1) Gold-Tipped Fiber 45cm Kit, Catalog Number: 11403301; 2) Gold-Tipped Fiber 65cm Kit, Catalog Number: 11403302; 3) Gold-Tipped Fiber 90cm Kit, Catalog Number: 11403304. Product Usage:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1464-2013·2013-06-05

    Talenti Roman Raspberry Sorbetto Recalled for Undeclared Pecans

    Talenti Gelato is recalling 16 fl oz Roman Raspberry Sorbetto containers in Indiana due to undeclared pecans.

    Product
    Talenti Roman Raspberry Sorbetto, 16fl oz, Crafted by Talenti, Marietta, GA 30062
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1403-2013·2013-06-05

    PTS Glucose Test Strips Recalled for Under-Recovery of Glucose

    Polymer Technology Systems is recalling PTS Glucose Test Strips because internal testing showed under-recovery of glucose, which could lead to inaccurate readings.

    Product
    PTS PANELS, Glucose Test Strips for use with CardioChek Brand Analyzers Product Usage: used by healthcare professionals and individuals with diabetes to measure glucose in whole blood
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1401-2013·2013-06-05

    Alere hCG Combo Cassette Kits Recalled for Incorrect Packaging Inserts

    Alere San Diego, Inc. is recalling 3,975 hCG Combo Cassette kits because some were packaged with the wrong product insert.

    Product
    Alere" hCG Combo Cassette (20/10 mIU/mL) Kit. Product Usage: The AlereTM hCG Combo (20/10 mIU/mL) test is a rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in serum or urine, as an aid in the early detection of pregnancy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1427-2013·2013-06-05

    Intuitive Surgical Recalls 8mm Cannulas for Labeling Clarification

    Intuitive Surgical is recalling 8mm cannulas to clarify existing labeling information and operating procedures.

    Product
    Cannula 8MM Regular. Provides the means of introduction and placement of an instrument or accessory into the human body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1424-2013·2013-06-05

    Intuitive Surgical Recalls da Vinci TORS User Manual Addendum

    Intuitive Surgical is recalling 1,374 user manual addenda for the da Vinci Surgical System to remove an indication and amend warnings for Transoral Surgery.

    Product
    User Manual addendum, TORS for da Vinci Surgical System IS 1200, IS 2000 and IS 3000. Product Usage: The user manual for Transoral Surgery (TORS) provided information to update and replace the Indications for Use and Representative uses section and add the section Warnings f
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-500-2013·2013-06-05

    Mylan Recalls Mislabelled Ropinirole Hydrochloride Tablets Due to Strength Error

    Mylan Pharmaceuticals is recalling 3,048 bottles of Ropinirole hydrochloride tablets because 3 mg bottles were incorrectly labeled as 4 mg.

    Product
    Ropinirole hydrochloride tablets, USP 4 mg, 100-count bottle (NDC 0378-5504-01), Rx only, Manufactured for: Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A. Made in India
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1423-2013·2013-06-05

    Becton Dickinson Recalls BBL DrySlide Oxidase Kits Due to Packaging Error

    Becton Dickinson is recalling BBL DrySlide Oxidase Kits because they were placed in incorrect packaging for distribution to laboratories.

    Product
    BBL DrySlide Oxidase Kit, catalog number 231746 Product Usage: Presumptive diagnostic aid for gram-negative bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1425-2013·2013-06-05

    Intuitive Surgical Recalls Tip Cover Accessories for Labeling Clarification

    Intuitive Surgical is recalling 50,000 boxes of Tip Cover Accessories for the da Vinci Surgical System to clarify existing labeling and related cautions.

    Product
    Tip Cover Accessory, 8 MM, MCS, box of 10 Product Usage: The disposable Tip cover accessory is used in conjunction with the 8mm Monopolar Curved Scissors Instruments to cut and coagulate tissue. The tip cover is intended to provide electrical insulation over a section of the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1415-2013·2013-06-05

    Spinal Solutions Recalls Loaner Bins and Sterilization Trays for Missing Instructions

    Spinal Solutions, LLC is recalling 56 loaner bins and sterilization trays because directions for use and surgical techniques were not provided to every physician.

    Product
    12mm x 27mm x 8mm 12mm x 27mm x 9mm 12mm x 27mm x 10mm 12mm x 27mm x 11mm 12mm x 27mm x 12mm 12mm x 27mm x 13mm 12mm x 27mm x 14mm Product Usage: Spinal Solutions distributes a variety of spinal fixation devices in loaner bins or on consignment. The company has de
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1422-2013·2013-06-05

    Becton Dickinson Recalls BBL DrySlide PYR Kits Due to Packaging Error

    Becton Dickinson is recalling 610 BBL DrySlide PYR Kits because they were placed in incorrect packaging for distribution to laboratories.

    Product
    BBL DrySlide PYR Kit, catalog number 231747 Product Usage: Presumptive diagnostic aid for group A streptococci and group D enterococci bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1428-2013·2013-06-05

    Intuitive Surgical Recalls da Vinci Flush Ports for Labeling Clarification

    Intuitive Surgical is recalling da Vinci instrument flush ports to clarify existing labeling and operating procedures.

    Product
    Flush Port (used in almost all da Vinci instruments) Assists in cleaning the instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1386-2013·2013-06-05

    Orthopedic Alliance Recalls Loaner Bin and Sterilization Trays for Missing Instructions

    Orthopedic Alliance LLC is recalling 26 loaner bins and sterilization trays because directions for use and surgical techniques were not provided to every physician for every surgery.

    Product
    Ball Head, 28 Short CERAMIC Ball Head, 28 Medium CERAMIC Ball Head, 28 Long CERAMIC Ball Head, 32 Short CERAMIC Ball Head, 32 Medium CERAMIC Ball Head, 32 Long CERAMIC Ball Head, 28 Short CoCr Ball Head, 28 Medium CoCr Ball Head, 28 Long CoCr Ball Head, 28 X-Long CoCr B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1429-2013·2013-06-05

    Intuitive Surgical da Vinci Si Surgeon Console Labeling Clarification

    Intuitive Surgical is clarifying labeling and operating procedures for the da Vinci Si Surgeon Console to ensure accurate control of endoscopic instruments.

    Product
    da Vinci Si Surgeon Console. Intended to assist in the accurate Control of Intuitive Surgical Endoscopic Instruments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1426-2013·2013-06-05

    Intuitive Surgical Recalls Unapproved da Vinci Thyroidectomy Promotional Literature

    Intuitive Surgical is recalling promotional literature for the da Vinci Surgical System's thyroidectomy indication because the use was not approved with a 510(k) change.

    Product
    Thyroidectomy Indication for the da Vinci Surgical Systems; Product Usage: da Vinci Thyroidectomy offers a minimally invasive surgery for both partial and total thyroidectomy procedures, including endoscopic and video assisted procedure that are preferable to conventional (op
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-498-2013·2013-06-05

    Aurobindo Recalls Lisinopril Tablets Due to Labeling Error

    Aurobindo Pharma USA Inc is recalling specific lots of Lisinopril 30 mg tablets because the label displays the incorrect strength on the side panel.

    Product
    LISINOPRIL — LISINOPRIL (LISINOPRIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1456-2013·2013-06-05

    Meijer Fruit Cups Recalled for Nutrition Labeling Errors

    Meijer Distribution is recalling specific fruit cups because the serving size was updated but the nutrition facts were not.

    Product
    Meijer Mandarin Oranges in Fruit Juice 8oz cup
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1455-2013·2013-06-05

    Meijer Fruit Cups Recalled for Nutrition Labeling Errors

    Meijer Distribution is recalling diced pears, peaches, and mandarin oranges in fruit juice 8 oz cups because the nutrition facts panel reflects the wrong serving size.

    Product
    Meijer Diced Peaches in Fruit Juice 8oz cup
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1454-2013·2013-06-05

    Meijer Diced Pears Recalled for Nutrition Labeling Error

    Meijer Distribution is recalling Diced Pears in Fruit Juice 8oz cups because the nutrition facts label reflects the wrong serving size.

    Product
    Meijer Diced Pears in Fruit Juice 8oz cup
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1436-2013·2013-05-29

    Go Max Go Foods Recalls Vegan Candy Bars for Undeclared Milk

    Go Max Go Foods is recalling Mahalo Candy Bars labeled as dairy-free because they contain undeclared milk.

    Product
    Mahalo Candy Bar. Coconut & almonds in a a rice-milk chocolately coating, 2.0 oz, gluten-free,dairy-free & vegan, no trans fats, nothing artificial. Distributed by Go Max Go Foods, LLC 40 Paseo Del Antilope, Santa Fe, NM 87506.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1439-2013·2013-05-29

    Frozen White Fish Balls Recalled for Missing Egg and Fish Species Labeling

    Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg and the specific fish species.

    Product
    Lam Sheng Kee, Frozen White Fish Ball - Fish Package Egg, Net Weight 7 oz (200 G) - Sheng Lin Mark Trade Co. LTD 4 F. No 89, Ln. 528 Heping Road, Bade City, Taoyuan County 334, Taiwan (ROC). Distributed by: Win Luck Trading Inc. 100 Pulaski Street, Bayonne, NJ 07002. UPC 69496
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1438-2013·2013-05-29

    Frozen Fish Balls Recalled for Missing Allergen and Fish Species Labeling

    Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg and the specific fish species.

    Product
    Lam Sheng Kee, Frozen White Fish Ball - Lobster Ball Net Weight 7 oz (200 G) - Sheng Lin Mark Trade Co. LTD 4 F. No 89, Ln. 528 Heping Road, Bade City, Taoyuan County 334, Taiwan (ROC). Distributed by: Win Luck Trading Inc. 100 Pulaski Street, Bayonne, NJ 07002. UPC 694968280
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1440-2013·2013-05-29

    Frozen White Fish Ball Recalled for Missing Allergen and Fish Species Labeling

    Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg as an ingredient and did not declare the species of fish.

    Product
    Lam Sheng Kee, Frozen White Fish Ball - Fresh Fish Cake, Net Weight 7 oz (200 G) - Sheng Lin Mark Trade Co. LTD 4 F. No 89, Ln. 528 Heping Road, Bade City, Taoyuan County 334, Taiwan (ROC). Distributed by: Win Luck Trading Inc. 100 Pulaski Street, Bayonne, NJ 07002. UPC 6949
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1437-2013·2013-05-29

    Frozen Fish and Shrimp Balls Recalled for Allergen Mislabeling

    Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Ball - Shrimp Ball because the label failed to list egg and the fish species.

    Product
    Lam Sheng Kee, Frozen White Fish Ball - Shrimp Ball Net Weight 7 oz (200 G) - Sheng Lin Mark Trade Co. LTD 4 F. No 89, Ln. 528 Heping Road, Bade City, Taoyuan County 334, Taiwan (ROC). Distributed by: Win Luck Trading Inc. 100 Pulaski Street, Bayonne, NJ 07002. UPC 69496828046
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1370-2013·2013-05-29

    Stryker Triathlon Femoral Distal Augment Recalled for Packaging Label Errors

    Stryker Howmedica Osteonics is recalling 11 units of Triathlon Femoral Distal Augments due to external packaging label errors, including an incorrect glyph and missing size reference.

    Product
    Stryker Orthopaedics Triathlon Femoral Distal Augment- Left; 1 single unit per package Howmedica Osteonics Corp. 325 Corporate Drive, Mahwah, NJ 07430 USA Stryker France, ZAC Satolas Green Pusignan, Av de Satoles Green 69881 Meyzieu, Cedex, France This device is used w
    Category
    Medical Device
    Distribution
    Distributed nationwide