The Recall Desk

State

Indiana product recalls

73,566 recalls have nationwide distribution and so reach Indiana. 9,592 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,592
Critical
1,913
Severe
2,529
Most recent
2026-10-24

Of the 9,592 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,529 (26%) are Severe.

These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27076–27100 of 83158

  • HighNHTSA·21V497000·2021-07-01

    2021 GMC Canyon Vehicles Recalled for Incorrect Tire Load Capacity Label

    General Motors is recalling 7,199 2021 GMC Canyon vehicles because the tire and loading information placard lists load capacity 51 pounds higher than intended, increasing the risk of vehicle overload and crashes.

    Product
    GMC — GMC CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21759·2021-07-01

    The Best Damn Liquids Liquid Nicotine Recalled for Non-Child-Resistant Packaging

    TBD Liquids is recalling approximately 1,000 units of The Best Damn Liquids branded liquid nicotine because the packaging is not child-resistant as required by law. Liquid nicotine is toxic if swallowed or absorbed through skin or eyes.

    Product
    The Best Damn Liquids branded liquid nicotine
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V502000·2021-07-01

    2021 Aprilia Tuono 660 and RS 660 recalled for engine crankshaft defect

    Aprilia is recalling 2021 Tuono 660 and RS 660 motorcycles because the engine crankshaft connecting rod may break due to improper heat-treatment, risking sudden engine stall and crash.

    Product
    APRILIA — APRILIA TUONO 660, RS 660
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·21758·2021-07-01

    Rejuvenation Deep Frame Mirrors Recalled for Laceration Hazard

    Rejuvenation is recalling about 3,325 Deep Frame Mirrors because the adhesive securing the mirror glass can fail, causing the glass to detach and fall out of the frame. Rejuvenation has received 18 reports of glass detaching, though no injuries have been reported.

    Product
    Deep Frame Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0634-2021·2021-06-30

    PremierZEN Platinum 8000 Capsules Recalled for Undeclared Drug Ingredients

    PremierZEN Platinum 8000 capsules, distributed nationwide, are being recalled because the product contains undeclared pharmaceutical ingredients (Sildenafil and Tadalafil) and was marketed without FDA approval.

    Product
    PremierZEN Platinum 8000 capsule, 1-count blister card (UPC 7 28175 42185 6), packaged in 12 cards per box (UPC 7 28175 42183 2), Distributed by: New Premier Group, Los Angeles, CA 90006
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0633-2021·2021-06-30

    PremierZEN Gold 7000 Capsule Recalled for Undisclosed Drug Contamination

    PremierZEN Gold 7000 capsules are recalled nationwide because the product contains undisclosed pharmaceutical ingredients Sildenafil and Tadalafil and was marketed without FDA approval.

    Product
    PremierZEN Gold 7000 capsule, 1-count blister card, packaged in 12 cards per box (UPC 7 28175 42183 2), Distributed by: New Premier Group, Los Angeles, CA 90006
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0635-2021·2021-06-30

    maXXzen Platinum 12000 Capsule Recalled for Undisclosed Drug Contaminants

    The FDA is recalling maXXzen Platinum 12000 capsules distributed nationwide because the product was marketed without an approved application and contains undisclosed pharmaceutical ingredients (Sildenafil and Tadalafil).

    Product
    maXXzen Platinum 12000 capsule, 1-count blister card (UPC 7 18122 04072 8), Distributed by: Maxx Inc, Los Angeles, CA 90028
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1863-2021·2021-06-30

    Nitric Oxide Delivery System Dosing Deficiency During Console Transitions

    GENOSYL DS Nitric Oxide Delivery System is recalled for delivering below-intended doses during transitions between primary and backup consoles following a software update.

    Product
    GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0688-2021·2021-06-30

    Clio Coconut Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Coconut Less Sugar Yogurt Bars (45g and 50g 10-packs) distributed nationwide due to possible metal fragments in the product.

    Product
    Clio Coconut Less Sugar Yogurt Bars wrapped in a Chocolate Coating 45g x 10 Clio Retail 10-pack and 50g x 10 Clio Retail 10-pack, UPC codes: 854021008237 and 854021008046
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1934-2021·2021-06-30

    Dexcom G6 Sensor 3-Pack Recalled for Temperature-Related Measurement Errors

    Cardinal Health is recalling 2,357 kits of Dexcom G6 Sensor 3-Pack due to temperature exposure during shipping that may cause inaccurate glucose readings. Affected units were distributed in Florida, Georgia, and South Carolina.

    Product
    DEXCOM G6 SENSOR 3 PACK Item Number: 5447552
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1930-2021·2021-06-30

    FREESTYLE LIBRE 14 DAY glucose monitoring system recalled for temperature exposure

    Cardinal Health is recalling 8,959 glucose monitoring kits due to temperature exposure during shipping that may result in inaccurate readings. Affected devices were distributed nationwide.

    Product
    FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SYSTEM. Item Number: 5479084
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1931-2021·2021-06-30

    FreeStyle Libre 2 Glucose Monitoring System Recalled for Inaccurate Results

    Cardinal Health is recalling FreeStyle Libre 2 glucose monitoring systems shipped between February and March 2021 due to temperature exposure during shipment that may cause inaccurate readings.

    Product
    FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0694-2021·2021-06-30

    Clio Peanut Butter Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Peanut Butter Greek Yogurt Bars due to the possible presence of metal fragments. The affected product was distributed nationwide with best-buy dates between March 7, 2021 and June 20, 2021.

    Product
    Clio Peanut Butter Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 854021008039
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1944-2021·2021-06-30

    FilmArray Pneumonia Panel diagnostic test kits recalled for false results

    BioFire Diagnostics is recalling 9 FilmArray Pneumonia Panel test kits due to manufacturing defects causing false positive and negative test results, as well as control failures.

    Product
    FilmArray Pneumonia Panel (Penumo) REF RFIT-ASY-0144
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21156·2021-06-30

    Children's Nightgowns Recalled for Flammability Standard Violation

    Auranso Official children's nightgowns sold on Amazon fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries. About 8,000 units distributed January–June 2021 are affected.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1939-2021·2021-06-30

    OneTouch Delica Lancets Recalled Due to Temperature Exposure During Shipping

    Cardinal Health is recalling OneTouch Delica Lancets (100-count boxes) after devices were exposed to freezing temperatures during shipping, which may affect blood glucose test accuracy. No injuries have been reported.

    Product
    ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0687-2021·2021-06-30

    Clio Coconut Greek Yogurt Bars recalled for possible metal fragments

    Clio LLC is recalling Clio Coconut Greek Yogurt Bars in 50g x 10-pack format due to the possible presence of metal fragments. The product was distributed nationwide.

    Product
    Clio Coconut Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC: 854021008046
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21159·2021-06-30

    Children's Robes Fail Federal Flammability Standards, Pose Burn Risk

    SIORO-branded children's robes sold on Amazon from December 2020 through April 2021 fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries to children.

    Product
    Children's Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0685-2021·2021-06-30

    Clio Strawberry Greek Yogurt Mini Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Strawberry Greek Yogurt Mini Bars (6.2 oz pouch x 6 pouches per case, UPC 854021008084) with best buy dates between 2/7/2021 and 6/27/2021 due to possible metal fragments.

    Product
    Clio Strawberry Greek Yogurt Mini Bars wrapped in a Chocolate Coating 6.2oz pouch x 6 pouches per case, UPC: 854021008084
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0703-2021·2021-06-30

    Favorite Day Peanut Butter Monster Trail Mix Recall for Plastic Contamination

    John B. Sanfilippo & Son Inc. is recalling Favorite Day Peanut Butter Monster Trail Mix because the product may contain stringy pieces of flexible plastic. The affected product was distributed nationwide.

    Product
    favorite day peanut butter monster Trail Mix, Product Number 04316. Peanuts, peanut butter chips, raisins, M&M'S peanut butter chocolate candies, peanut butter pretzel balls, and mini peanut butter cups. Net Wt 14 oz. (396g), UPC 85239-15684
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21158·2021-06-30

    UPPAbaby RumbleSeat Adapters Recalled for Child Fall Hazard

    UPPAbaby is recalling approximately 86,000 RumbleSeat adapters that can detach from strollers, posing a fall hazard to children. The company has received 135 reports of detachments, including injuries such as bumps, scrapes, and two broken noses.

    Product
    UPPAbaby adapters included with Rumbleseats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0691-2021·2021-06-30

    Clio Mixed Berry/Peach Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Mixed Berry/Peach Greek Yogurt Bars sold at Costco due to possible metal fragments in the product. Consumers should not consume the affected items.

    Product
    Clio Mixed Berry / Peach Greek Yogurt Bars wrapped in a Chocolate Coating Costco Club pack Clio 50g x 16 (12pc tray), UPC code: 854021008220
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1946-2021·2021-06-30

    Medical Action Curved Hemostats recalled due to flaking metal risk

    Medical Action Industries is recalling curved hemostats distributed across 16 U.S. states due to a manufacturing defect causing potential metal flaking and discoloration.

    Product
    Medical Action INDUSTRIES INC., Disposable Instrument Pack Curved Hemostat, REF 56224
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0695-2021·2021-06-30

    Clio Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Raspberry/Peach Sams Mini Club Yogurt Bars due to the possible presence of metal fragments. The recalled product was distributed nationwide.

    Product
    Clio Raspberry / Peach Sams Mini Club Yogurt Bars wrapped in a Chocolate Coating 24g x 24 (12pc tray), UPC code: 854021008251
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1903-2021·2021-06-30

    Blood Culture Identification Panel Recalled Due to Manufacturing Defect

    BioFire BCID2 panels for FilmArray Systems are recalled due to manufacturing defects causing elevated rates of false negative results. Affected diagnostic kits may fail to detect infections in blood culture samples.

    Product
    BioFire BCID2 Panel, REF RFIT-ASY-0147, For FilmArray Systems, CE, Blood Culture Identification Panel in vitro diagnostic, Rx Only, UDI: (01)00815381020338
    Category
    Medical Device
    Distribution
    Distributed nationwide