The Recall Desk

State

Indiana product recalls

73,388 recalls have nationwide distribution and so reach Indiana. 9,587 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,587
Critical
1,913
Severe
2,528
Most recent
2026-09-30

Of the 9,587 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.

Which agencies issued them

These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22951–22975 of 82975

  • ModerateFDA (Drugs)·D-0823-2022·2022-05-04

    Testosterone Cypionate Recalled Due to Manufacturing Quality Control Deviations

    Olympia Compounding Pharmacy is recalling Testosterone Cypionate 200 mg/mL due to failure to properly investigate manufacturing process monitoring deviations that occurred before October 2021. The recall affects 7,161 vials distributed nationwide.

    Product
    Testosterone Cypionate 200 mg/mL (in Grapeseed Oil), Packaged in a) 10 mL Multi-Dose vial, NDC 73198-0054-10; b) 5 mL Multi-Dose vial, NDC 73198-0054-05, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0818-2022·2022-05-04

    Alprostadil Injectable Drug Recalled for Manufacturing Quality Control Deviations

    Olympia Compounding Pharmacy is recalling 460 vials of Alprostadil 80 mcg/mL due to manufacturing quality control deviations related to improper investigation of environmental and personnel monitoring excursions prior to October 2021.

    Product
    PGE-2, Alprostadil 80 mcg/mL, 10ml Multi-Dose vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0029-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0817-2022·2022-05-04

    PGE-1 Alprostadil Injection Recalled for Manufacturing Process Deviations

    Olympia Compounding Pharmacy is recalling 821 vials of PGE-1 Alprostadil 40 mcg/mL injection nationwide. The recall is due to Current Good Manufacturing Practice deviations in environmental and personnel monitoring procedures that were not properly investigated.

    Product
    PGE-1, Alprostadil 40 mcg/mL, 10ml Multi-Dose vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0028-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1004-2022·2022-05-04

    IV Start Kit Convenience Kits Recalled for Manufacturing Test Validation Issue

    ROi CPS LLC is recalling 290 convenience kits containing IV Start Kits due to potential inadequacy in the validation of test methods used during manufacturing. Distribution was in Missouri.

    Product
    Convenience kits containing regard IV Start Kits: (1) regard Clinical Packaging Solutions, Item Number: 830014015, LD00199O - C Section Mother; and (2) regard Clinical Packaging Solutions, Item Number: 830014016, LD00199P - C Section Mother.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0827-2022·2022-05-04

    Sincalide Injectable Vials Recalled for Manufacturing Monitoring Failures

    Olympia Compounding Pharmacy is recalling 1,770 vials of Sincalide due to CGMP deviations in environmental and personnel monitoring. The manufacturer failed to properly investigate monitoring excursions prior to October 2021.

    Product
    Sincalide. Lyophilized powder for reconstitution. 5 mcg per Multi-Dose vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0082-00.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1006-2022·2022-05-04

    IV Start Kit convenience kits recalled for manufacturing validation defect

    ROi CPS LLC recalled 950 IV Start Kit convenience kits due to potential inadequacy in manufacturing test method validation. No injuries reported.

    Product
    Convenience kits containing regard IV Start Kits: regard Clinical Packaging Solutions, Item Number: 830110002, IV01121B - IV Start Labor Birth.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0825-2022·2022-05-04

    Ultratest testosterone injection recalled for manufacturing monitoring deviations

    Olympia Compounding Pharmacy recalled 1,276 vials of Ultratest testosterone injection nationwide. Prior to October 2021, the manufacturer failed to properly investigate environmental and personnel monitoring deviations per FDA manufacturing standards.

    Product
    Ultratest, Testosterone Cypionate 160 mg/mL, Testosterone Propionate 40 mg/mL, 10 mL Multi-Dose vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0058-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0820-2022·2022-05-04

    Olympia Compounding Pharmacy recalls T-50 injectable medication for manufacturing quality control deviations

    Olympia Compounding Pharmacy is recalling T-50 injectable medication nationwide due to manufacturing quality control failures. Environmental and personnel monitoring controls were not properly investigated prior to October 2021.

    Product
    T-50, Papaverine 8 mg/mL . Phentolamine 0.29 mg/mL . Alprostadil 2.9 mcg/mL, 10ml Multi-Dose vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0022-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0792-2022·2022-05-04

    Drug Recall: Zonisamide Capsules Due to Manufacturing Deviations

    Glenmark Pharmaceuticals is recalling 12,003 bottles of Zonisamide 50 mg capsules nationwide due to manufacturing deviations.

    Product
    ZONISAMIDE — ZONISAMIDE (ZONISAMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V295000·2022-05-03

    2022-2023 Mack Granite Trucks Recalled for Insufficient Brake Air Tank Volume

    Mack is recalling 2022-2023 Granite trucks because the air tanks lack sufficient volume for proper brake system operation. Insufficient air can reduce braking performance and increase crash risk. Dealers will install replacement air tanks at no charge.

    Product
    MACK — MACK GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V293000·2022-05-03

    Cruiser Shadow Cruiser Travel Trailer Recall for LP Gas Leak Risk

    Cruiser RV is recalling 2022 Shadow Cruiser travel trailers because cracked LP gas fittings may cause a gas leak, increasing fire risk.

    Product
    CRUISER RV — CRUISER RV SHADOW CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V296000·2022-05-03

    2022 Tesla Model 3 Infotainment CPU Failure Risk During Fast Charging

    Tesla is recalling 2022 Model 3 vehicles where the infotainment CPU may overheat during fast charging, causing the center display to lag or restart, potentially preventing critical safety information from displaying.

    Product
    TESLA — TESLA MODEL S, MODEL X, MODEL Y, MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V292000·2022-05-03

    2022 DRV Mobile Suites and Full House Recreational Vehicles LP Gas Leak Recall

    DRV is recalling 88 model-year 2022 Mobile Suites and Full House fifth wheel recreational vehicles with cracked quick disconnect fittings in the LP gas system. The defect may cause gas leaks that could increase the risk of fire.

    Product
    DRV — DRV MOBILE SUITES, FULL HOUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V290000·2022-05-03

    Jayco and Entegra Recreational Vehicles Power Steering Line Defect

    Certain 2021-2022 Jayco and Entegra recreational vehicles have a defective power steering line connection that could result in sudden loss of power steering and brake assist, increasing crash risk. Dealers will replace the lines at no cost.

    Product
    JAYCO — JAYCO, ENTEGRA GREYHAWK, REDHAWK, ESTEEM, GREYHAWK PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V289000·2022-05-02

    KZRV Travel Trailers Recalled for Cracked LP Gas Fittings

    KZRV recreational trailers and fifth wheels may have cracked LP gas fittings that can leak, creating a fire hazard. Dealers will replace fittings free of charge.

    Product
    KZRV — KZRV CONFLUENCE, DURANGO, DURANGO GOLD, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·012-2022·2022-04-29

    Wayne Farms Recalls Undercooked Ready-to-Eat Chicken Breast Fillets

    Wayne Farms is recalling approximately 30,285 pounds of ready-to-eat chicken breast fillets that may be undercooked. The recall was initiated after a customer complaint.

    Product
    Wayne Farms LLC — Wayne Farms, LLC Recalls Ready-to-Eat Chicken Breast Fillet Products That May Be Undercooked
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V287000·2022-04-28

    Micro Bird Recalls Transit and School Buses for Electrical Fire Risk

    Micro Bird is recalling 2006-2021 transit and school buses because a damaged electrical harness may short circuit and cause a fire.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, G5 SCHOOL BUS, MB II SCHOOL BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V284000·2022-04-28

    2021 Jeep Grand Cherokee Recalled for Sticking EGR Valve

    Chrysler is recalling 2021 Jeep Grand Cherokee and Dodge Durango vehicles due to EGR valve defects that may cause loss of drive power and increase crash risk. Dealers will provide free replacement.

    Product
    JEEP — JEEP, DODGE GRAND CHEROKEE 4XE, DURANGO, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22127·2022-04-28

    Electric Start Pressure Washers Recalled for Carbon Monoxide Hazard

    Generac Power Systems is recalling about 53,000 Generac and DR Power electric start pressure washers because the electronic start/stop button can malfunction and cause the unit to self-start, posing a carbon monoxide poisoning risk in confined spaces.

    Product
    Electric Start Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22126·2022-04-28

    Bed Bath & Beyond Recalls Woven Bunny Baskets Due to Choking Hazard

    Bed Bath & Beyond is recalling H for Happy™ Woven Bunny Baskets because the plastic eyes can detach, posing a choking hazard to young children. About 12,800 units were sold at Bed Bath & Beyond stores and online in March 2022.

    Product
    H for Happy™ Woven Bunny Baskets
    Category
    Consumer Product
    Distribution
    Distributed nationwide