The Recall Desk

State

Indiana product recalls

73,478 recalls have nationwide distribution and so reach Indiana. 9,589 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,589
Critical
1,913
Severe
2,528
Most recent
2026-10-14

Of the 9,589 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 2,528 (26%) are Severe.

These figures cover only the 9,589 recalls whose distribution notice names Indiana specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23826–23850 of 83067

  • SevereFDA (Food)·F-0770-2022·2022-03-02

    Dole Asian Island Crunch salad recalled for Listeria monocytogenes

    Dole Fresh Vegetables Inc is recalling Dole 13 oz Asian Island Crunch salad due to Listeria monocytogenes detected in harvest equipment. Products were distributed across multiple US states and Canadian provinces.

    Product
    Dole 13 oz Asian Island Crunch / Croustillante Des Iles Asiatiques UPC: 0-71430-01721-0 SKU: 930
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0785-2022·2022-03-02

    Little Salad Bar Garden Salad recalled for Listeria in harvest equipment

    Dole Fresh Vegetables Inc is recalling Little Salad Bar 12 oz Garden Salad because harvest equipment used in production tested positive for Listeria monocytogenes. Approximately 578,243 cases were distributed to Ohio and California, with broader distribution across multiple U.S. states and Canadian provinces.

    Product
    Little Salad Bar 12 oz Garden Salad UPC: 4099100082982 SKU: 3210
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0771-2022·2022-03-02

    Dole Southwest Salad Kit Recalled Due to Listeria Contamination Risk

    Dole Fresh Vegetables Inc is recalling its 13 oz Southwest Salad Kits due to Listeria monocytogenes detected in harvest equipment. Consumers should not consume affected products with best-by dates December 22, 2021 through January 9, 2022.

    Product
    Dole 13 oz Southwest Salad Kit UPC: 0-71430-01701-2 SKU: 2776
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0750-2022·2022-03-02

    Dole Garden Salad Recalled for Listeria Contamination on Harvest Equipment

    Dole recalled 3-pound garden salads after harvest equipment tested positive for Listeria monocytogenes. Affected product codes begin with B, with best-by dates December 23, 2021–January 8, 2022.

    Product
    Dole 3lb Garden Salad UPC:0-71430-01138-6 SKU: 2163
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0791-2022·2022-03-02

    Marketside 24 oz Classic Iceberg Salad Recalled for Listeria Contamination

    Dole Fresh Vegetables is recalling Marketside 24 oz Classic Iceberg Salad due to Listeria monocytogenes found on harvest equipment used to prepare the product. Distribution included all US states and parts of Canada.

    Product
    Marketside 24 oz Classic Iceberg Salad UPC: 6-81131-32895-1 SKU: 3193
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0781-2022·2022-03-02

    Dole recalls Kroger 24 oz lettuce salad due to Listeria

    Dole Fresh Vegetables is recalling Kroger 24 oz Classic Garden lettuce salad because harvest equipment was found contaminated with Listeria monocytogenes. Consumers should not eat the affected product.

    Product
    Kroger 24 oz Classic Garden UPC: 0-11110-91037-0 SKU: 3009
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0746-2022·2022-03-02

    Dole Country Ranch Lettuce Kit Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Dole 13.25oz Country Ranch Kits after Listeria monocytogenes was detected in harvest equipment. Products have best-by dates from December 23, 2021 through January 8, 2022.

    Product
    Dole 13.25oz Country Ranch Kit UPC:0-71430-01730-2 SKU: 761
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0772-2022·2022-03-02

    Dole Southwest Salad Kit recalled for Listeria contamination in harvest equipment

    Dole Fresh Vegetables Inc recalled its 13 oz Southwest Salad Kit after Listeria monocytogenes was detected in harvest equipment used for the raw iceberg lettuce. The company is asking consumers not to consume the product.

    Product
    Dole 13 oz Southwest Salad Kit / Salade du Sud-ouest UPC: 0-71430-01711-1 SKU: 2976
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0749-2022·2022-03-02

    Dole Garden Salad recalled due to Listeria contamination

    Dole Fresh Vegetables is recalling Dole 24oz Value Size Garden Salad due to Listeria monocytogenes contamination found in harvest equipment. Best-by dates December 23, 2021 through January 8, 2022 are affected.

    Product
    Dole 24oz Value Size Garden Salad UPC:0-71430-01136-2 SKU: 2109
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0744-2022·2022-03-02

    Dole Iceberg Lettuce Recalled Due to Listeria Contamination

    Dole Fresh Vegetables is recalling 12oz iceberg lettuce packages because harvest equipment was found to contain Listeria monocytogenes.

    Product
    Dole 12oz American UPC:0-71430-00933-8 SKU: 43
    Category
    Food
    Distribution
    37 states
  • SevereNHTSA·22V118000·2022-03-02

    Freightliner M2 Brake Drum Defect May Cause Loss of Brake Function

    Daimler Trucks is recalling certain 2020-2022 Freightliner M2 trucks due to brake drum cracking that can cause brake failure and increase crash risk. All vehicles have been remedied.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0645-2022·2022-03-02

    RISE UP RED EDITION Capsules recalled for undeclared tadalafil

    RISE UP RED EDITION Capsules, 650 mg, have been recalled because they contain undeclared tadalafil, an ingredient found in FDA-approved male sexual enhancement products. The product is an unapproved drug and was distributed nationwide via Amazon Marketplace.

    Product
    RISE UP RED EDITION Capsules, 650 mg, 10-count blisters packaged in a carton, ASIN B08JCWG84D, barcode X002NI8PE1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0776-2022·2022-03-02

    Dole Peppercorn Ranch Chopped Kit Recalled Due to Listeria in Harvest Equipment

    Dole Fresh Vegetables recalls 9.1 oz Peppercorn Ranch Chopped Kits due to Listeria monocytogenes found in harvest equipment. The affected products were distributed across Canada and the United States.

    Product
    Dole 9.1 oz Peppercorn Ranch Chopped Kit UPC: 0-71430-00093-9 SKU: 728
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0778-2022·2022-03-02

    Kroger American Blend Lettuce Recalled for Listeria Contamination Risk

    Dole Fresh Vegetables recalls Kroger American Blend lettuce due to Listeria found on harvest equipment. Affected products distributed across the US and Canada have best-by dates from December 22, 2021 to January 9, 2022.

    Product
    Kroger 12 oz American Blend UPC: 0-11110-91041-7 SKU: 3003
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0769-2022·2022-03-02

    Dole Garden Salad Recalled Due to Listeria Contamination in Harvest Equipment

    Dole Fresh Vegetables Inc is recalling multiple sizes of Dole Garden Salad due to Listeria monocytogenes found in harvest equipment used during lettuce harvesting.

    Product
    Dole 12 oz Garden Salad / Salade du Jardin UPC: 0-71430-01135-5 SKU: 2673 Dole 2 lb Garden Salad UPC: 0-71430-01137-9 SKU 2504 Dole 24 oz Value Size Garden Salad UPC: 0-71430-01136-2 SKU 2109
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0779-2022·2022-03-02

    Dole Fresh Vegetables Recalls Kroger Salad Mix for Listeria

    Dole Fresh Vegetables recalled Kroger 12 oz Classic Garden salad mix after Listeria monocytogenes was found in harvest equipment. Affected products have codes beginning with W and best-by dates from December 22, 2021 through January 9, 2022.

    Product
    Kroger 12 oz Classic Garden UPC: 0-11110-91036-3 SKU: 3007
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0751-2022·2022-03-02

    Dole Shredded Lettuce Recalled Due to Listeria Monocytogenes Contamination

    Dole Fresh Vegetables Inc is recalling 8oz packages of shredded lettuce because harvest equipment was found to contain Listeria monocytogenes. The recalled products have best-by dates from December 23, 2021 through January 8, 2022.

    Product
    Dole 8oz Shredded Lettuce UPC: 0-71430-01065-5 SKU: 2029
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0777-2022·2022-03-02

    Dole Teriyaki Pineapple Kit recalled for Listeria contamination

    Dole is recalling certain Teriyaki Pineapple Kits due to Listeria monocytogenes detected in harvest equipment. Affected products have codes beginning with W and best-by dates from December 22, 2021 through January 9, 2022.

    Product
    Dole 9.8 oz Chopped Teriyaki Pineapple Kit UPC: 0-71430-00100-4 SKU: 791 Dole 9.8 oz Chopped Teriyaki Pineapple Kit / Teriyaki A L'ananas UPC: ¿0-71430-00182-0 SKU 1014
    Category
    Food
    Distribution
    37 states
  • HighFDA (Devices)·Z-0672-2022·2022-03-02

    Biomet Shoulder Implant Stem Recalled for Inadequate Coating Adhesion

    Biomet is recalling a Comprehensive Shoulder System implant component due to a defect in the porous plasma coating. The coating may not have sufficient adhesion strength, compromising the implant's structural integrity.

    Product
    Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 14 MM, 55 MM Long Item Number: 113614
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0665-2022·2022-03-02

    BD Vacutainer Luer Lok Access Device may shed particles causing false test results

    BD's Vacutainer Luer Lok Access Device may release contaminant particles that can be misidentified as red blood cells in laboratory analysis, potentially leading to false elevated RBC counts.

    Product
    BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port equipped with a threaded female luer during blood or urine sample collection using evacuated BD Vacutainer Blood or Urine Collection Tubes Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0670-2022·2022-03-02

    Hip implant revision system recalled due to inadequate coating adhesion

    Biomet is recalling 19 units of the Arcos Modular Revision Hip System because an incorrect rework process may have weakened the coating's adhesion strength, posing a potential implant failure risk.

    Product
    Arcos Modular Revision Hip System, Standard Cone Prox Body, Porous Plasma,Size A, 60 MM Item Number: 11-301301
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0658-2022·2022-03-02

    NobelReplace dental implant components recalled for driver engagement defect

    Nobel Biocare is recalling 702 NobelReplace dental implant components due to a manufacturing defect that prevents proper driver engagement. The defect could result in aborted or delayed surgical procedures.

    Product
    NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22091·2022-03-02

    Petzl PIRANA Descender Canyoneering Devices Recalled for Drowning Risk

    Petzl is recalling about 3,450 PIRANA descender canyoneering devices because the rope can get caught in the blocking slot, stopping or suspending the climber and creating a drowning risk under waterfalls or pools.

    Product
    PIRANA descender canyoneering devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0669-2022·2022-03-02

    RESODURA Matrix Onlay Recalled Due to Unsealed Packaging

    Collagen Matrix is recalling RESODURA matrix onlay dural substitutes due to outer packaging that is not properly sealed, potentially compromising sterility and creating a risk of infection.

    Product
    RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated as dural substitutes for the repair of dura matter. REF: DUMO10125
    Category
    Medical Device
    Distribution
    Distributed nationwide