The Recall Desk

Hazard

Regulatory Violation recalls

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

What the numbers show

Total
91
Critical
1
Severe
43
Most recent
2026-05-13

Of the 91 regulatory violation recalls we have scored against our rubric, 1 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 43 (47%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all regulatory violation 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.

26–50 of 91

  • ModerateFDA (Food)·F-0070-2021·2020-11-04

    Capital Seaboard Recalls Frozen Raw Shrimp Due to Import Alert Violation

    Capital Seaboard is recalling Gracie's Pointe frozen raw shrimp because it was inadvertently released for distribution while under an FDA import alert.

    Product
    Gracie's Pointe frozen raw shrimp. 1. 8/12 Count Per Pound Tail On, UPC: 849558095034 2. 21/25 Count Per Pound Tail Off, UPC: 849558095065 3. 31/40 Count Per Pound Tail Off, UPC: 849558095072 4. 16/20 Count Per Pound EZ Peel UPC: 849558095003 5. 16/20 Count Per Pound Tail O
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-1310-2020·2020-06-24

    EcoLips Sport Lip Balm Recalled for Excessive Avobenzone Concentration

    Eco Lips Inc. is recalling 68,400 tubes of EcoLips Sport Lip Balm, SPF 30, because the avobenzone concentration exceeds FDA limits.

    Product
    EcoLips Sport Lip Balm, SPF 30, Avobenzone (5%), Octinoxate (10%), Octisalate (5%), Net Wt. 0.15 oz. (4.25g) tube, Eco Lips, Inc., Marion, IA 52302, UPC: 859623000030; 859623000177; 859623000573; Display UPC: 859623000092; 859623000108; 859623000139; 859623000146; 859623000184; 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1600-2020·2020-04-08

    Butterfly iQ Ultrasound System Auto Bladder Volume Tool Recalled for Regulatory Violation

    Butterfly Network, Inc. is recalling the Butterfly iQ Ultrasound System Auto Bladder Volume Tool because it was distributed without an approved 510(k).

    Product
    Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder Volume Tool is a segmentation measurement tool REF/Model: 850-20003 Software versions 1.13.0, 1.14.0, and 1.15.0 - Product Usage: Butterfly iQ is indicated for use by qualified and trained healthcare pr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0190-2020·2019-11-13

    Basic Reset Recalls Nuovi Firming Masque for Lack of FDA Approval

    Basic Reset Inc. is recalling 339 bottles of Nuovi Firming Masque because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).

    Product
    Nuovi Firming Masque, Renew and Reset, 2 fl. oz. 59 mL bottle, Made in USA exclusively for Basic Reset 260 W. Main St., Ste 103 Hendersonville, TN 37075
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-1342-2019·2019-05-22

    FDA Orders Recall of Juices International 12-Ounce Glass Bottled Juices

    Juices International is recalling 12-ounce glass bottled juices in the New York area due to a violation of a Consent Decree of Injunction.

    Product
    All Juice Drinks and Beverages in 12 ounce glass bottles including but not limited to Agony, Double Trouble, Front End Lifter, Irish (sea) Moss, Cashew Punch, Carrot Juice, Sorrel, Carrots & Beet, Carrot & Ginger, Ginger Beer, Pineapple Twist. Keep Refrigerated
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0774-2019·2018-12-26

    Luckyberry Recalls Unpasteurized Cold-Pressed Juice for Regulatory Violation

    Luckyberry is recalling unpasteurized Mai Tai and Orange Pineapple cold-pressed juices sold in Lawrence, Kansas, due to violations of FDA juice safety regulations.

    Product
    Luckyberry Cold-Pressed Juice, Mai Tai, Orange Pineapple, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0770-2019·2018-12-26

    Luckyberry Recalls Unpasteurized Cold-Pressed Spicy Ginger Juice

    Luckyberry is recalling unpasteurized Spicy Ginger cold-pressed juice sold in Lawrence, KS, due to a violation of FDA juice safety regulations.

    Product
    Luckyberry Cold-Pressed Juice, Spicy Ginger, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0771-2019·2018-12-26

    Luckyberry Recalls Unpasteurized Cold-Pressed Juice for Regulatory Violations

    Luckyberry is recalling unpasteurized cold-pressed juice products distributed in Lawrence, Kansas, due to violations of FDA juice safety regulations.

    Product
    Luckyberry Cold-Pressed Juice, Seasonal Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0772-2019·2018-12-26

    Luckyberry Cold-Pressed Beetnik Juice Recalled for Unpasteurized Status

    Luckyberry is recalling cold-pressed Beetnik juice sold in Lawrence, KS, because the product was manufactured and distributed in violation of FDA regulations requiring pasteurization.

    Product
    Luckyberry Cold-Pressed Juice, Beetnik, Orange, Red Beet, Kale, Cucumber, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0769-2019·2018-12-26

    Luckyberry Recalls Unpasteurized Cold-Pressed Juice for Regulatory Violation

    Luckyberry is recalling unpasteurized cold-pressed juice sold in Lawrence, Kansas, due to violations of FDA juice safety regulations.

    Product
    Luckyberry Cold-Pressed Juice, Merc Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0768-2019·2018-12-26

    Luckyberry Cold-Pressed Juice Recalled for Unpasteurized Juice Violation

    Luckyberry is recalling cold-pressed juice products because they were manufactured and distributed in violation of FDA regulations requiring pasteurization or HACCP compliance.

    Product
    Luckyberry Cold-Pressed Juice, Clean & Clear, Pineapple, Green Apple, Cucumber, Min, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0766-2019·2018-12-26

    Luckyberry Cold-Pressed Juice Recalled for Unpasteurized Juice Violations

    Luckyberry is recalling cold-pressed juice products sold in Lawrence, KS, because they were manufactured and distributed in violation of FDA regulations requiring pasteurization.

    Product
    Luckyberry Cold-Pressed Juice, NoCoast, Kale, Cucumber, Green Apple, Celery, Lemon, Ginger, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0767-2019·2018-12-26

    Luckyberry Recalls Unpasteurized Cold-Pressed Juice for Regulatory Violation

    Luckyberry is recalling unpasteurized cold-pressed juice products because they were manufactured and distributed in violation of FDA regulations.

    Product
    Luckyberry Cold-Pressed Juice, Reset, Carrot, Apple, Ginger, Lemon, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0773-2019·2018-12-26

    Luckyberry Cold-Pressed Juice Recalled Due to Violation of Juice HACCP Regulations

    Luckyberry is recalling certain unpasteurized cold-pressed juice products because they were manufactured and distributed in violation of juice safety regulations.

    Product
    Luckyberry Cold-Pressed Juice, Spicy Watermelon, Watermelon, Red Beet, Lime, Mint, Green Apple, Jalepeno, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereUSDA FSIS·061-2018·2018-07-14

    Beautiful Pig Recalls Uninspected Pork and Beef Products

    The Beautiful Pig, Inc. is recalling ready-to-eat and raw pork and beef products produced without USDA inspection. The products were distributed in Oregon and Washington.

    Product
    The Beautiful Pig, Inc. Recalls Ready-To-Eat And Raw Pork And Beef Products Produced Without The Benefit Of Inspection And Shipped Under U.S. Retention
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0621-2018·2018-02-21

    Aesculap ELAN 4 Burr and Blade Accessories Recalled for Regulatory Violation

    Aesculap Implant Systems LLC is recalling ELAN 4 burr and blade accessories because they were marketed without 510(k) premarket notification clearance.

    Product
    ELAN 4 Blade: ELAN 4 1-RING PIN CUTTER D1.0 ELAN 4 1-RING NEURO CUTTER+ SOFT D1.5 ELAN 4 1-RING NEURO CUTTER+ SOFT D2.0 ELAN 4 1-RING NEURO CUTTER+ SOFT D2.5 ELAN 4 1-RING NEURO CUTTER SOFT D3.0 ELAN 4 1-RING NEURO CUTTER+ SOFT D3.0 ELAN 4 1-RING NEURO CUTTER D2.0 ELAN 4
    Category
    Medical Device
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1084-2017·2017-08-23

    FDA Recalls Ultra-Sten Capsules Marketed Without Approval

    Hardcore Formulations is recalling Ultra-Sten capsules because they contain unapproved ingredients and were marketed without an approved NDA or ANDA.

    Product
    ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1054-2017·2017-01-04

    Sunset Natural Products Recalls Jagra Dietary Supplement Under Consent Decree

    Sunset Natural Products Inc. is recalling Jagra Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured or distributed since April 2014.

    Product
    Jagra Dietary Supplement (unknown container size)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1061-2017·2017-01-04

    Sunset Natural Products Recalls Super Vita Green Dietary Supplement

    Sunset Natural Products Inc. is recalling Super Vita Green Dietary Supplement pursuant to a consent decree requiring the destruction of products manufactured since April 2014.

    Product
    Super Vita Green Dietary Supplement (unknown container size)
    Category
    Food
    Distribution
    2 states