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.

8701–8725 of 9611

  • ModerateFDA (Devices)·Z-1366-2013·2013-05-29

    DePuy Recalls AltrX Hip Liners Due to Incorrect Box Labeling

    DePuy Orthopaedics is voluntarily recalling 20 AltrX Polyethylene Acetabular Liners because the boxes were incorrectly labeled with the wrong product specifications.

    Product
    Pinnacle Hip Solutions ALTRX Polyethylene Acetabular Liner, Ref 1221-36-452 Product Usage: An acetabular liner is used in combination with other implants for total hip arthroplasty is intended to provide increased patient mobility and reduce pain by replacing the damaged hip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1217-2013·2013-05-29

    Cefla Dental X-Ray Units Recalled for Missing Safety Labels

    Cefla Dental Group is recalling 173 MyRay RXDC dental x-ray units because they lack required certification and identification labels.

    Product
    MyRay RXDC dental unit x-ray unit
    Category
    Medical Device
    Distribution
    22 states
  • ModerateFDA (Devices)·Z-1341-2013·2013-05-29

    Coloplast Recalls Mislabeled Restorelle L Prostheses Due to Incorrect Instructions

    Coloplast is recalling 111 units of Restorelle L prostheses because the packaging contains incorrect Instructions For Use pamphlets.

    Product
    Rostorelle L, Polypropylene Mesh, Catalog number 501440, Manufacturer Coloplast A/S 3050 Denmark.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1344-2013·2013-05-29

    Alere Recalls Cardinal Health hCG Cassette Rapid Test Due to Packaging Error

    Alere San Diego is recalling 2,167 Cardinal Health hCG Cassette Rapid Test kits because they were incorrectly packaged in boxes for a different test type.

    Product
    Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in urine, as an aid in the early detection of pregnancy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-420-2013·2013-05-29

    Novartis Recalls Lamisil AT Antifungal Cream Due to Illegible Labeling

    Novartis Consumer Health is recalling 3,828 tubes of Lamisil AT antifungal cream because the lot and expiration dates may be illegible.

    Product
    Lamisil AT (terbinafine hydrochloride cream 1% antifungal), 24 g (.85 oz) tube, Novartis Consumer Health, Parsippany, NJ 07054, NDC 0067-6171-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1179-2013·2013-05-29

    Chicago X-Ray Systems Recalls IntraOs 70 X-Ray Systems for Labeling Defects

    Chicago X-Ray Systems is recalling 1,960 IntraOs 70 intra-oral x-ray systems because they have missing or incomplete labels and user manual information.

    Product
    Fona Srl IntraOs 70 intra-oral x-ray system IntraOS 70 is an extra oral source X-ray system for dental radiographic examination and diagnosis of diseases of the teeth.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1384-2013·2013-05-22

    Heartland Gourmet Gluten-Free Cookie Mix Recalled for Undeclared Milk

    Heartland Gourmet is recalling gluten-free double chocolate cookie mix labeled as dairy-free because some products contain milk.

    Product
    Heartland Gourmet Gluten Free double chocolate cookie mix, DAIRY FREE, packaged in 16-oz. boxes. Manufactured by: Heartland Gourmet, LLC, Lincoln, NE.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1385-2013·2013-05-22

    Heartland Gourmet Gluten Free Cookie Mix Recalled for Undeclared Milk

    Heartland Gourmet is recalling specific lots of gluten-free chocolate chip cookie mix labeled as dairy-free because they contain milk.

    Product
    Heartland Gourmet Gluten Free chocolate chip cookie mix, DAIRY FREE, packaged in 16-oz. boxes. Manufactured by: Heartland Gourmet, LLC, Lincoln, NE.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1408-2013·2013-05-22

    Lisy Corp. Recalls Sazonador de Carnes Meat Seasoning for Undeclared Soy

    Lisy Corp. is recalling Sazonador de Carnes meat seasoning in 5 oz, 14 oz, and 28 oz sizes due to undeclared soy. The product was distributed in 12 states.

    Product
    Sazonador de Carnes (Meat Seasoning) in 5 oz, 14 oz, and 28 oz
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1381-2013·2013-05-22

    Early Bird Foods Recalls Granola Snack Mix for Undeclared Soya Lecithin

    Early Bird Foods & Co. is recalling CHOC-A-DOODLE-DOO granola snack mix due to undeclared soya lecithin. The product was distributed in six states.

    Product
    Early Bird Foods & Co. CHOC-A-DOODLE-DOO featuring DARK CHOCOLATE & COCONUT granola snack mix, Net Wt. 12 oz packaged in clear plastic bag. Each case contains 12 packages. UPC: 6 89466 30000 0.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1409-2013·2013-05-22

    Lisy Corp. Recalls Sazon Perfecta Seasoning Due to Undeclared Soy

    Lisy Corp. is recalling Sazon Perfecta seasoning in 4 oz, 12 oz, and 24 oz packages because it contains undeclared soy.

    Product
    Sazon Perfecta (Perfect Seasoning) in 4 oz, 12 oz, and 24 oz
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1405-2013·2013-05-22

    Gruma Senora Verde Taco Dinner Kit Recalled for Undeclared Wheat

    Gruma Corp is recalling Senora Verde Taco Dinner Kits because they contain undeclared wheat, posing a risk to individuals with wheat allergies or celiac disease.

    Product
    Senora Verde Taco Dinner Kit, 12ct, 9.75 oz (276g), 12 cartons per case.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1386-2013·2013-05-22

    Heartland Gourmet Gluten Free Pizza Crust Mix Recalled for Milk Mislabeling

    Heartland Gourmet is recalling gluten-free pizza crust mix labeled as dairy-free but containing milk. The recall affects 204 boxes distributed to schools, online, and retail in TX, MN, CO, and Canada.

    Product
    Heartland Gourmet Gluten Free rosemary basil pizza crust mix, DAIRY FREE, packaged in 15.4-oz. boxes. Manufactured by: Heartland Gourmet, LLC, Lincoln, NE.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1404-2013·2013-05-22

    Nuts Are Good! Recalls Island Mix for Undeclared Allergens

    Nuts Are Good! Inc. is recalling Island Mix because it contains undeclared peanuts, cashews, and almonds, posing a risk to allergic consumers.

    Product
    Island Mix, 12 oz. with best by date of 02/17/2014
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1321-2013·2013-05-22

    QIAGEN CMV PCR Kits Recalled for Incorrect Vial Mixture

    QIAGEN is recalling artus CMV RG PCR kits because they may contain incorrect vials mixed with correct ones, potentially affecting test accuracy.

    Product
    QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223) Product Usage: The artus CMV RG PCR ASR is designed to detect and to quantify nucleic acid specific to human cytomegalovirus (CMV) using real-time PCR technology (PCR) in the Rotor-Gene 2000/3000 (RG).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1319-2013·2013-05-22

    Summit Medical Recalls Myringotomy Lance Blades Due to Incorrect Packaging

    Summit Medical is recalling Myringotomy Lance Blades because the boxes contain the wrong type of blade.

    Product
    Summit Medical, BL-2006, Myringotomy Lance (Juvenile) Blade, Sterile P, Summit Medical, Inc., 815 Northwest Parkway, Suite 100, St. Paul, MN 55121 Use to make an incision in the tympanic membrane.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-319-2013·2013-05-22

    Walmart Amlodipine Tablets Recalled for Labeling Error

    Legacy Pharmaceutical Packaging is recalling Walmart Amlodipine Besylate Tablets 10 mg due to a label error listing 5 mg in the USP description.

    Product
    Walmart Amlodipine Besylate Tablets, USP 10 mg, Rx only, 30 tablets, Manufactured by: InvaGen Pharmaceuticals, Inc., Hauppauge, NY. Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR. Packaged by: Legacy Pharmac
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1320-2013·2013-05-22

    QIAGEN CMV PCR Kits Recalled for Incorrect Vial Mixture

    QIAGEN is recalling artus CMV RG PCR kits because they may contain incorrect vials mixed with correct ones, potentially affecting test accuracy.

    Product
    QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225) Product Usage: Test is intended for use in the detection and quantitation of human cytomegalovirus (CMV) specific DNA, as part of an in house validated real-time PCR assay. One service package containing the handbook
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1331-2013·2013-05-22

    DePuy LifeLiner Gloves Recalled for Mispackaging

    DePuy Orthopaedics is recalling LifeLiner Stick and Cut Resistant Gloves because right-handed packages contained left-handed gloves.

    Product
    DePuy LifeLiner Stick & Cut Resistant Gloves Rt, Lg Part No. 5200-68-000 The gloves are designed to resist sticks and cuts and are not cut or puncture proof. These gloves are not required by any surgical technique.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1392-2013·2013-05-22

    Juice Bar Solutions Recalls Add a Scoop Probiotic Due to Labeling Error

    Juice Bar Solutions is recalling 26 containers of Add a Scoop Probiotic because the label claimed the product was GMO-free, but manufacturer paperwork did not support this claim.

    Product
    Add a Scoop by Smoothie Essentials; Probiotic; Supports Digestive Health, dietary supplement; Net Weight: 1 lb (464g) 16 oz. Contains Bacillus Coagulans GBI-30-6086 in a base of Maltdextrin. Gluten Free, GMO Free Manufactured for: Juice Bar Solutions, 38 Maybeck St., Novato
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-1272-2013·2013-05-15

    Siemens MicroScan MICroSTREP panels recalled for false susceptibility results

    Siemens is recalling MicroScan MICroSTREP plus Type 1 panels because they may produce false antimicrobial susceptibility results for Streptococcus agalactiae.

    Product
    Siemens Healthcare Diagnostics Inc. MIcroScan MICroSTREP plus Type 1 B1027-201 panels. .MICroSTREP panels are designed for use in determining antimicrobial agent susceptibility of aerobic nonenterococcal streptococci (including Streptococcus pneumoniae) and Haemophilus spp.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1234-2013·2013-05-15

    Stryker Irrigator Tips Recalled for Incorrect Sterilization Temperature Instructions

    Stryker Endoscopy is recalling reusable irrigator tips because the instructions listed the wrong pre-vacuum steam sterilization temperature.

    Product
    Stryker Irrigator Reusable Tips: Vented Tip, 5mm X 45cm Non-Reflective with 30¿ Downward Bend At Proximal End. Suction irrigator tips aid in cleaning and clearing the operative site during laparoscopic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1224-2013·2013-05-15

    Stryker Irrigator Tips Recalled for Incorrect Sterilization Temperature Instructions

    Stryker Endoscopy is recalling reusable irrigator tips because the instructions listed incorrect pre-vacuum steam sterilization temperatures.

    Product
    Stryker Irrigator Reusable Tips: 5mm X 24cm Regular Tip, Vented, Metal Finish. Suction irrigator tips aid in cleaning and clearing the operative site during laparoscopic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide