The Recall Desk

State

Indiana product recalls

72,940 recalls have nationwide distribution and so reach Indiana. 9,555 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,555
Critical
1,903
Severe
2,136
Most recent
2026-09-09

Of the 9,555 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,136 (22%) are Severe.

These figures cover only the 9,555 recalls whose distribution notice names Indiana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3601–3625 of 82495

  • ModerateFDA (Devices)·Z-1195-2026·2026-02-04

    Central line dressing change kits recalled over cracking adhesive tubing

    Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.

    Product
    Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG, Kit SKU DT22880; 2) ADULT CVC DRSG CHG W/ADHESIVE, Kit SKU DYNDC3283A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1194-2026·2026-02-04

    Head shave latex safe kits recalled over cracking adhesive tubing

    Medline is recalling 60 units of the Head Shave-Latex Safe Kit because it contains MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked.

    Product
    Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE KIT, Kit SKU P903933B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1190-2026·2026-02-04

    Head and neck procedure packs recalled over cracking adhesive tubing

    Medline is recalling 40 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.

    Product
    Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS, Kit SKU CDS984347O; 2) HEAD AND NECK CDS-LF, Kit SKU CDS984857N; 3) NECK PACK-LF, Kit SKU DYNJ0966130K; 4) NECKLINE PACK-LF, Kit SKU DYNJ51440B; 5) THYROID PACK, Kit SKU DYNJ58742J; 6) ENT I, K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1193-2026·2026-02-04

    BEAR implants recalled over an expiration date beyond approved shelf life

    Miach Orthopaedics is recalling 284 BEAR Implants because the label carries an expiration date that extends beyond the product's documented and approved shelf life.

    Product
    Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY, Kit SKU ACC010270A; 2) DRAWER 2, Kit SKU ACC010690; 3) DRAWER 3 SYR/DRS/MON/NG 1 OF 3, Kit SKU ACC011073; 4) HYPOSPADIUS PACK, Kit SKU DYNJ00282Q; 5) SJ NEURO PACK RFID-LF, Kit SKU DYNJ0101360K;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1191-2026·2026-02-04

    Laparoscopy procedure packs recalled over cracking MASTISOL adhesive tubing inside

    Medline is recalling 456 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.

    Product
    Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF, Kit SKU DYNJ19974P; 2) DEPAUL ABDOMINAL ENDOSCOPY-LF, Kit SKU DYNJ20027K; 3) LAPAROSCOPY PACK-LF, Kit SKU DYNJ20468J; 4) SMJ LAPAROSCOPY PACK, Kit SKU DYNJ25763N; 5) SMJ LAPAROSCOPY PACK,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1200-2026·2026-02-04

    Spine and hip procedure packs recalled over cracking adhesive tubing

    Medline is recalling 117 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.

    Product
    Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M; 2) SM-SPINE PACK-LF, Kit SKU DYNJ0395037X; 3) TOTAL HIP PACK, Kit SKU DYNJ04809N; 4) MAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN; 5) SCC/SPOC HAND & FOOT PACK, Ki
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2026·2026-02-04

    Breast biopsy and dermatology packs recalled over cracking adhesive tubing

    Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.

    Product
    Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF, Kit SKU CDS984853L; 2) BREAST BIOPSY PACK, Kit SKU DYNJ45641B; 3) DERMATOLOGY PACK, Kit SKU DYNJT3658A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1177-2026·2026-02-04

    Alphenix INFX-8000F systems recalled over ceiling suspension screws that loosen

    Canon Medical Systems is recalling 98 units of the Alphenix INFX-8000F because fixing screws of the ceiling movement gear in the ceiling suspended arm may become loose.

    Product
    Alphenix INFX-8000F, interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1176-2026·2026-02-04

    Alphenix INFX-8000C systems recalled over ceiling suspension screws that loosen

    Canon Medical Systems is recalling 172 units of the Alphenix INFX-8000C because fixing screws of the ceiling movement gear in the ceiling suspended arm may become loose.

    Product
    Alphenix INFX-8000C, interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0297-2026·2026-02-04

    Mouthwash recalled over missing or illegible lot and expiry coding

    Haleon is recalling 84,764 bottles of parodontax Active Gum Health Mouthwash, Mint, over the potential for missing or illegible lot and expiration date coding on the bottles.

    Product
    PARODONTAX — PARODONTAX (CETYLPYRIDINIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V061000·2026-02-03

    Ford Recalls 2023-2024 Transit Vehicles Due to Engine Crossmember Defect

    Ford is recalling 2023-2024 Transit vehicles because an improperly secured engine crossmember may cause the engine to shift, potentially leading to loss of drive power or brake failure.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V062000·2026-02-03

    Ford Recalls 2026 E-Transit Vehicles Due to Battery Fire Risk

    Ford is recalling 2026 E-Transit vehicles because missing washers in the high-voltage battery pack may cause electrical arcing, increasing the risk of fire or loss of drive power.

    Product
    FORD — FORD E-TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V060000·2026-02-02

    Pierce Recalls 2025 Vehicles Due to Steering Linkage Arm Bolt Issue

    Pierce Manufacturing is recalling 2025 Velocity, Arrow XT, Saber, Impel, and Enforcer vehicles because a steering linkage arm bolt may come loose, risking loss of steering control.

    Product
    PIERCE — PIERCE ENFORCER, IMPEL, VELOCITY, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V059000·2026-02-02

    Trucks and SUVs recalled over a trailer tow module design defect

    Chrysler is recalling 456,287 Ram and Jeep vehicles because an improperly designed trailer tow module may leave trailer lights unlit and trailer brakes inoperative.

    Product
    RAM — RAM, JEEP 5500, 1500, 4500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V058000·2026-01-30

    Grand Design motorhome front seat bases may be improperly tightened

    Grand Design is recalling certain 2025-2026 Lineage motorhomes because the seat base on the driver and front passenger seat may have been improperly tightened. This fails FMVSS 207.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V057000·2026-01-30

    Grand Design Recalls 2026 Solitude RVs for Fire Risk

    Grand Design is recalling 2026 Solitude recreational vehicles because a water tank heating pad may fail, increasing the risk of a fire.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V056000·2026-01-30

    BMW and Toyota Supra engine starters may overheat and catch fire

    BMW is recalling certain 2021-2024 BMW models and 2021-2023 Toyota Supra vehicles because the engine starter may overheat and catch fire due to wear on an internal component.

    Product
    BMW — BMW, TOYOTA 430I, Z4, 330I, 530I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V051000·2026-01-29

    Jeep Grand Cherokee rear coil springs may detach while driving

    Chrysler is recalling certain 2021-2023 Jeep Grand Cherokee L and 2022-2023 Grand Cherokee vehicles because the rear coil springs may be incorrectly installed and detach from the vehicle while driving.

    Product
    JEEP — JEEP GRAND CHEROKEE L, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V054000·2026-01-29

    Honda driver seat cushion frame may not have been tightened properly

    Honda is recalling certain 2023 Accord and Accord Hybrid, 2024 HR-V and Pilot, and Acura Integra vehicles because the driver's seat cushion frame may not have been tightened properly.

    Product
    HONDA — HONDA, ACURA ACCORD HYBRID, INTEGRA, ACCORD, HR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26219·2026-01-29

    Pull string teething toys recalled after fifteen reported choking incidents

    About 49,410 AiTuiTui Pull String Teething Toys are being recalled. CPSC is aware of 15 choking incidents and two incidents of children able to bite pieces off the silicone strings.

    Product
    AiTuiTui Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26230·2026-01-29

    Glow-in-the-dark crayon sets recalled over high strontium and aluminum levels

    About 600 Primark The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets are being recalled because the crayons have high levels of strontium and aluminum.

    Product
    Primark The Nightmare Before Christmas Glow-in-the-Dark Coloring Set
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26220·2026-01-29

    Electric bicycle rear wheel bolts recalled over breakage when torqued

    About 19,890 rear wheel bolts on 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles are being recalled because the bolts can break when torqued, causing wheel separation.

    Product
    Rear wheel bolts installed on model year 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26221·2026-01-29

    Multivitamin bottles recalled over caps that are not child-resistant

    About 148,370 Mindbodygreen Ultimate Multivitamin+ bottles are being recalled because the packaging holding iron-containing supplements is not child-resistant.

    Product
    Ultimate Multivitamin+ Dietary Supplement Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide