The Recall Desk

State

Indiana product recalls

73,597 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
1,908
Severe
2,534
Most recent
2026-10-24

Of the 9,592 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,534 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29501–29525 of 83189

  • SevereFDA (Drugs)·D-0123-2021·2020-12-16

    Shilpa Medicare Recalls Azacitidine Injection Vials Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 6,560 vials of Azacitidine for Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall is voluntary and nationwide.

    Product
    Azacitidine for Injection 100 mg/vial, For Subcutaneous and Intravenous Use Only, Rx Only, One Single Dose Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72606-558-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0154-2021·2020-12-16

    Chef Myron's Teriyaki Sauce Recalled for Gluten-Free Mislabeling

    JMH International is recalling Chef Myron's Premium Teriyaki Sauce because it contains wheat-derived gluten despite a gluten-free claim.

    Product
    Chef Myron's Premium Teriyaki Sauce, 64 FL OZ (1.89 L), Item # 400023118, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0541-2021·2020-12-16

    Clinical Innovations Recalls ROM Plus Collection Kits Due to Swab Defect

    Clinical Innovations is recalling ROM Plus Collection Kits because incorrect swabs may cause false test results.

    Product
    Clinical Innovations ROM Plus Collection Kit IFU: ROM Plus Rupture of Membrane Test ROM-5025, ROM-6025
    Category
    Medical Device
    Distribution
    8 states
  • HighCPSC·21053·2020-12-16

    Camp Chef Recalls Portable Gas Stoves Due to Fire Hazard

    Camp Chef is recalling about 20,600 portable gas stoves because a sharp edge on an internal gas regulator part can cause gas leaks, posing a fire hazard.

    Product
    Camp Chef portable stoves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0560-2021·2020-12-16

    Medtronic Evolut PRO System Recalled for Potential Valve Leaflet Damage

    Medtronic is recalling 71,030 Evolut PRO System units worldwide due to a potential for transcatheter aortic valve leaflet damage during post-implant balloon dilatation.

    Product
    Evolut (TM) PRO System. With the following model numbers: a. EVOLUTPRO-23, Labeled as: VLV EVOLUTPRO-23 PRO COMM 29L OUS, VLV EVOLUTPRO-23 BLUE 29L COMM OUS, VLV EVOLUTPRO-23 BLUE COMM JPN, VLV EVOLUTPRO-23 BLUE 6L COMM OUS, VLV EVOLUTPRO-23 PRO COMM 29L CAN, VLV…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0557-2021·2020-12-16

    Mani Trocar Kit 23G S Recalled for Luer Connector Defects

    Mani, Inc. is recalling Trocar Kit 23G S units because Luer connector dimensions are out of specification, which may cause fluid leakage or disconnection during ophthalmic surgery.

    Product
    MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0165-2021·2020-12-16

    Kroger HomeChef Pretzel-Crusted Chicken Meal Kits Recalled for Listeria Risk

    Kroger is recalling HomeChef Pretzel-Crusted Chicken meal kits because a supplier ingredient was suspect for Listeria species.

    Product
    HomeChef Meal kit:One-Sheet Pretzel-Crusted Chicken with roasted broccoli and honey mustard..31.0 OZ (1 LB 15 OZ) 879g
    Category
    Food
    Distribution
    33 states
  • HighCPSC·21052·2020-12-16

    Graco Recalls Inclined Sleeper Accessory for Four Playard Models

    Graco is recalling inclined sleeper accessories for four playard models due to a risk of infant suffocation. Consumers should stop using the accessory immediately and contact Graco for a refund.

    Product
    Inclined sleeper accessory included with the Graco Pack 'n Play Day2Dream Playard with Bedside Sleeper, Graco Pack 'n Play Nuzzle Nest Playard, Graco Pack 'n Play Everest Playard and Graco Pack 'n Play Rock 'n Grow Playard
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0544-2021·2020-12-16

    Philips IntelliVue X2 Multi Measurement Server Speaker Failure Recall

    Philips is recalling 16 IntelliVue X2 Multi Measurement Servers because speaker failures may prevent audible alarms, potentially delaying patient treatment.

    Product
    Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0556-2021·2020-12-16

    Shimadzu MH-200S X-Ray System Recalled for Ceiling Arm Software Defect

    Shimadzu Medical Systems is recalling 22 MH-200S X-Ray systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.

    Product
    MH-200S, system with Ceiling Suspended C-arm Support - Product Usage: intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0559-2021·2020-12-16

    Medtronic Evolut R System Recalled for Potential Valve Leaflet Damage

    Medtronic is recalling Evolut R System transcatheter aortic valves due to a potential risk of leaflet damage during post-implant balloon dilatation.

    Product
    Evolut (TM) R System. With the following model numbers: a. EVOLUTR-23, Labeled as VLV EVOLUTR-23 VT IR 6L COMM OUS, VLV EVOLUTR-23 TAV EVOLUT R CE 29L MX, VLV EVOLUTR-23 TAV CE AU 2Y MX, VLV EVOLUTR-23 TAV JPN MX, VLV EVOLUTR-23 GREY 29L COMM OUS, VLV EVOLUTR-23 TAV EVOLUT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0542-2021·2020-12-16

    K2M Everest MI XT Tab Removal Tool Recalled for Cracking and Leakage

    K2M, Inc. is recalling 197 units of the Everest MI XT Tab Removal Tool because the threaded interface may crack, causing Loctite to leak from the handle.

    Product
    Everest MI XT Tab Removal Tool (i.e. All-In-One Tab Removal Tool)-used to break the tab off the Everest XT screw by rocking the instrument back and forth until the entire tab is fully detached from the screw head. Catalog number: 5101-90195
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0155-2021·2020-12-16

    Chef Myron's Szechuan Sauce Recalled for Gluten-Free Mislabeling

    JMH International is recalling Chef Myron's Szechuan Sauce because it contains wheat-derived fermented soy sauce despite a gluten-free claim.

    Product
    Chef Myron's Szechuan Sauce, 64 FL OZ (1.89 L), Item # 400023293, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0561-2021·2020-12-16

    Medtronic Evolut PRO+ System Recalled for Valve Leaflet Damage Risk

    Medtronic is recalling 19,961 Evolut PRO+ Transcatheter Aortic Valve systems due to a potential for leaflet damage during post-implant balloon dilatation.

    Product
    Evolut (TM) PRO+ System. With the following model numbers: a. EVPROPLUS-23US, Labeled as VLV EVPROPLUS-23US COMM JPN, VLV EVPROPLUS-23 COMM US; b. EVPROPLUS-26US, Labeled as VLV EVPROPLUS-26US COMM JPN, VLV EVPROPLUS-26 COMM US; c. EVPROPLUS-29US, Labeled as VLV…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0539-2021·2020-12-16

    Chromsystems Recalls MassChrom Amino Acid Analysis Plasma Control Level III

    Chromsystems Instruments & Chemicals GmbH is voluntarily recalling 342 vials of MassChrom Amino Acid Analysis Plasma Control Level III due to a Class II device defect.

    Product
    MassChrom Amino Acid Analysis Plasma Control Level III, Order No. 0473 - Product Usage: The kit is intended for amino acid metabolic screening, confirmation of a tentative diagnosis, and monitoring of treatment in individuals diagnosed with a metabolic disorder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0558-2021·2020-12-16

    MANI Infusion Cannula 23G S Recalled for Luer Connector Defects

    Mani, Inc. is recalling MANI Infusion Cannula 23G S units because Luer connector dimensions are out of specification, which may cause fluid leakage or unintended disconnection during ophthalmic surgery.

    Product
    MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery Ref: MTC 23S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0149-2021·2020-12-16

    Good & Gather Banana Chocolate Chip Date & Nut Bars Recalled for Undeclared Almonds

    Riverside Natural Foods is recalling Good & Gather Banana Chocolate Chip Date & Nut Bars because they contain undeclared almonds.

    Product
    Good & Gather Banana Chocolate Chip Date & Nut Bars, UPC 0 85239-04216 8. 5-1.6 oz (45g) Bars. Net Wt. 8oz (225g). DIST BY: Target Corporation, Minneapolis, MN 55403.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0166-2021·2020-12-16

    Kroger HomeChef Buffalo Pretzel Chicken Breast Meal Kit Recalled for Listeria Risk

    The Kroger Co is recalling 1,080 HomeChef meal kits because a supplier ingredient was suspect for Listeria species. No illnesses have been reported.

    Product
    HomeChef meal kit: Buffalo Pretzel Chicken Breast with Roasted Cauliflower and Broccoli. 29 ounce.
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-0545-2021·2020-12-16

    Philips IntelliVue MP2 Patient Monitors Recalled for Speaker Failure

    Philips is recalling two IntelliVue MP2 patient monitors because speaker failures may prevent audible alarms, potentially delaying patient treatment.

    Product
    Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport inside and outside…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0552-2021·2020-12-16

    TissueTech Recalls PROKERA Slim Corneal Bandages Due to Microbial Contamination

    TissueTech, Inc. is recalling 75 units of PROKERA Slim non-sterile biologic corneal bandages due to potential exposure to microbial contamination.

    Product
    PROKERA Slim, non-sterile - Product Usage: Biologic corneal bandage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0537-2021·2020-12-16

    Chromsystems MassChrom Amino Acid Analysis Plasma Control Level I Recalled

    Chromsystems Instruments & Chemicals GmbH is recalling MassChrom Amino Acid Analysis Plasma Control Level I kits because they do not meet stability criteria and may impact results.

    Product
    MassChrom Amino Acid Analysis Plasma Control Level I, Order No. 0471 - Product Usage: The kit is intended for amino acid metabolic screening, confirmation of a tentative diagnosis, and monitoring of treatment in individuals diagnosed with a metabolic disorder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0159-2021·2020-12-16

    Chef Myron's Premium Shoyu Sauce Recalled for Gluten-Free Mislabeling

    JMH International is recalling Chef Myron's Premium Shoyu Sauce because it contains wheat-derived gluten despite a gluten-free claim.

    Product
    Chef Myron's Premium Shoyu Sauce, 1 GAL (3.78 L), Item # 400023077, 2 bottles/case; 5 GAL (18.92 L), Item # 400023279, plastic pail
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21054·2020-12-16

    BRP Recalls Can-Am Off-Road Screw Jacks Due to Crush Hazard

    BRP is recalling Can-Am Off-Road screw jacks because they can collapse, posing a crush hazard that could cause severe injury or death.

    Product
    Can-Am® Off-Road screw jacks
    Category
    Consumer Product
    Distribution
    Distributed nationwide