The Recall Desk

State

Indiana product recalls

73,376 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.

These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20501–20525 of 82963

  • HighCPSC·23701·2022-10-06

    MillerKnoll Eames Desk and Storage Units Recalled for Lead Paint Violation

    MillerKnoll is recalling about 700 Eames Desk and Storage Units sold between October 2020 and March 2022 because the tan side panels contain lead paint levels exceeding the federal ban, posing a lead poisoning hazard to young children.

    Product
    Eames Desk Units and Eames Storage Units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23002·2022-10-06

    Hearth & Hand Tea Kettles Recalled for Fire and Burn Hazards

    Target is recalling about 12,800 Hearth & Hand with Magnolia Tea Kettles due to paint chipping that poses a fire hazard, and handle and spout defects that risk burn injuries. No injuries have been reported.

    Product
    Hearth & Hand™ with Magnolia Tea Kettles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23003·2022-10-06

    Swift Industries Recalls 9-Inch Rubber Straps for Bicycle Bags

    Swift Industries is recalling 9-inch rubber straps used to fasten bicycle bags because the straps can break, causing the bag to fall and creating a crash hazard to riders. No injuries have been reported.

    Product
    9-inch Swift Straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1802-2022·2022-10-05

    Keswick Creamery Recalls Bovre Cheese for Potential Listeria Contamination

    Keswick Creamery is recalling Bovre cheese in multiple flavors due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in Washington DC, Maryland, Virginia, and Pennsylvania.

    Product
    Bovre, multiple flavors: plain; oregano and garlic; herbes de Provence; cranberry and honey. 8oz clear deli container, expiration dates 7/25/22, 8/1/22, 8/8/22, 8/22/22
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1796-2022·2022-10-05

    Aged Raw Milk Cheese Recalled Due to Listeria Monocytogenes Risk

    Keswick Creamery at Carrock Farms LLC is recalling Vulkwin's Folly Scratch 2 aged raw milk cheese due to potential Listeria monocytogenes contamination. All products manufactured by the firm may be affected.

    Product
    Aged raw milk cheese "Vulkwin's Folly Scratch 2" 4oz-12oz packages
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1800-2022·2022-10-05

    Whole Milk Ricotta Cheese Recall Due to Listeria Contamination Risk

    Keswick Creamery is recalling Whole Milk Ricotta cheese sold at farm stores and farmers markets in DC, MD, VA, and PA regions due to potential Listeria monocytogenes contamination.

    Product
    Pasteurized milk cheese "Whole Milk Ricotta" 8 oz and 16 oz clear deli container, expiration dates 7/18/22, 7/25/22, 8/1/22, 8/8/22, 8/18/22
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1810-2022·2022-10-05

    Dutch Red Potatoes with Mustard Sauce Recalled for Undeclared Egg Allergen

    World Variety Produce is recalling Dutch Red Potatoes with Dijon Mustard Sauce because the sauce packet fails to declare the presence of egg, a common allergen. Consumers with egg allergies who consume the product risk allergic reactions.

    Product
    Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g) UPC code 0-45255-15221-0 Distributed by World Variety Produce, Inc. Los Angeles, CA Product of USA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1803-2022·2022-10-05

    Pasteurized Quark Cheese Recalled for Potential Listeria Contamination

    Keswick Creamery is recalling Pasteurized Quark cheese due to potential Listeria monocytogenes contamination. The cheese was distributed to farm stores and farmers markets in DC, Maryland, Virginia, and Pennsylvania.

    Product
    Pasteurized milk cheese "Quark", multiple flavors "Dill and Onion", and "Plain" 8 oz and 16 oz clear deli container, expiration dates 7/7/22, 8/4/22, 8/25/22
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-1763-2022·2022-10-05

    TANDEM LIFE controller software failures affecting cardiopulmonary bypass equipment nationwide

    FDA recalls TANDEM LIFE LivaNova LIFESPARC Controllers due to critical software failures that cause the device to freeze, crash, or stop displaying data. The controllers are used in cardiopulmonary bypass procedures.

    Product
    TANDEM LIFE LivaNova LIFESPARC Controller; Controller and Accessories Model 5900-0000; Controller Only Model 5900-0001. For circulatory or cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1798-2022·2022-10-05

    Aged Raw Milk Cheese Recalled for Listeria Contamination Risk

    Keswick Creamery recalls Calverley aged raw milk cheese due to potential Listeria monocytogenes contamination affecting products distributed to farm stores and farmers markets in DC, MD, VA, and PA.

    Product
    Aged raw milk cheese "Calverley" 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1801-2022·2022-10-05

    Pasteurized Havarti cheese recalled for potential Listeria contamination

    Keswick Creamery is recalling Havarti cheese due to potential Listeria monocytogenes contamination. All products manufactured by the firm may be affected.

    Product
    Pasteurized milk cheese "Havarti" 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1799-2022·2022-10-05

    Aged Raw Milk Feta Cheese Recalled for Listeria Risk

    Keswick Creamery is recalling aged raw milk feta cheese due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in DC, Maryland, Virginia, and Pennsylvania.

    Product
    Aged raw milk cheese "Feta" in 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·22V740000·2022-10-05

    Blue Bird Recalls 2022-2023 Vision Transit Buses Due to Fuel Leak Risk

    Blue Bird is recalling 2022-2023 Vision transit buses with 7.3L gasoline engines because a transmission cable may cause a fuel leak, increasing fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1795-2022·2022-10-05

    Aged raw milk cheese recalled for potential Listeria monocytogenes contamination

    Keswick Creamery is recalling Ploughman Cider Wash Tomme aged raw milk cheese (batch 47) due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in Washington DC, MD, VA, and PA.

    Product
    Aged raw milk cheese "Ploughman Cider Wash Tomme" batch 47 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1804-2022·2022-10-05

    Vermeer Cheese Products Recalled for Potential Listeria Contamination

    Keswick Creamery is recalling Vermeer Cheese due to potential Listeria monocytogenes contamination. Products were distributed to farm stores and farmers markets in Washington DC, Maryland, Virginia, and Pennsylvania.

    Product
    Vermeer Cheese in 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1805-2022·2022-10-05

    Alexia Organic Seasoned Hashed Browns recalled for potential Listeria contamination

    Lamb Weston Sales is recalling Alexia Organic Seasoned Hashed Browns Yukon Select Potatoes due to potential Listeria monocytogenes contamination. The frozen product was distributed nationwide and internationally.

    Product
    Item AX058, Alexia Organic Seasoned Hashed Browns Yukon Select Potatoes, 16 oz. bag, 12/16 oz. bags per case. Product is frozen and it's not ready to eat and labeled with cooking instructions. Produced by Lamb Weston, Kennewick, WA. UPC 8 34183 00303 5. Product contains…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1855-2022·2022-10-05

    Medline ClearPro Suction Catheter Connector May Separate During Use

    Medline ClearPro closed suction catheters may have a connector that separates from the device during patient suctioning. The malfunction affects 65,320 units distributed nationwide and internationally.

    Product
    MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. ET LENGTH DOUBLE SWIVEL, 12 Fr, Item Number/REF: DYNCPDS12; b. ET LENGTH DOUBLE SWIVEL, 14 Fr, Item…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1830-2022·2022-10-05

    Cope Mandril Wire Guide Guidewires Recalled for Packaging Seal Breach

    Cook Incorporated is recalling Cope Mandril Wire Guide stainless steel guidewires because the packaging chevron seal may be completely breached, compromising device sterility. Affected lots total 2,748 units in the US and 302 internationally.

    Product
    Cope Mandril Wire Guide (Stainless Steel), Stainless Steel Guidewire Reference Part Number/GPN PMG-18SP-60-COPE G05183 PMG-18SP-100-COPE G05822 PMG-18SP-125-COPE G10077
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1839-2022·2022-10-05

    Cook Roadrunner Guidewire Recalled for Compromised Sterile Packaging Seal

    Cook Incorporated is recalling Roadrunner PC Wire Guide guidewires due to a complete breach of the sterile packaging seal. The breach may compromise device sterility, affecting 202 units in the US and 11 internationally.

    Product
    Roadrunner PC Wire Guide (Nimble Floppy), Guidewire RFPC-35-145 G07914
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1840-2022·2022-10-05

    Cook Roadrunner PC Guidewire Recalled for Compromised Packaging Seal

    Cook Incorporated recalls Roadrunner PC Wire Guide devices due to a potential packaging seal breach that may compromise sterility. The recall affects 115 units distributed domestically and internationally.

    Product
    Roadrunner PC Wire Guide (The Firm LT), Guidewire Reference Part Number/GPN RLPC-35-145 G06866
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V741000·2022-10-05

    2023 BMW iX Transmission Defect Risk of Vehicle Rollaway

    BMW is recalling one 2023 iX with a defective transmission final drive gear weld that could break, causing vehicle rollaway if the parking brake is not engaged. Dealers will replace the electric drive unit at no cost.

    Product
    BMW — BMW IX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1826-2022·2022-10-05

    Bentson Wire Guide Devices Recalled for Potential Sterility Compromise

    Cook Incorporated is recalling Bentson Wire Guide devices due to potential packaging defects that may compromise device sterility.

    Product
    Bentson Wire Guide, Guidewire (OUS ONLY); Reference Part Number: TSMB-35-145 (GPN G27041)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1831-2022·2022-10-05

    Cook Medical Wire Guide Devices Recalled for Packaging Breach

    Cook Incorporated is recalling specific lots of Double Flexible Tipped Wire Guide Guidewire devices due to a complete breach of the packaging chevron seal, which may compromise sterility.

    Product
    Double Flexible Tipped Wire Guide, Guidewire Reference Part Number/GPN TDOC-35-145-0-3 G00362 C-TDOC-18-50-0-2 G05146 TDOC-35-50-0-3 G00364 C-DOC-21-40-0-2 G02431 C-TDOC-21-50-0-2 G05195 C-TDOC-25-50-0-2 G05145
    Category
    Medical Device
    Distribution
    Distributed nationwide