The Recall Desk

State

Indiana product recalls

73,741 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,596
Critical
1,908
Severe
2,534
Most recent
2026-10-28

Of the 9,596 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 9,596 recalls whose distribution notice names Indiana specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34101–34125 of 83337

  • HighFDA (Devices)·Z-0788-2020·2020-01-15

    Avanos Recalls Haylard Closed Suction Systems Due to Blocked Lumens

    Avanos Medical is recalling Haylard Closed Suction Systems for neonates and pediatrics because the central lumen may be blocked, potentially preventing adequate suctioning of airway secretions.

    Product
    Haylard Closed Suction System for Neonates/Pediatrics, 5 Fr, 1. REF 195, Y-Adapter, SAP Finished Product Code 109382303; 2. REF 201, with BALLARD Technology, SAP Finished Product Code 109382803; 3. REF 202, Elbow, SAP Finished Product Code 109382903; 4. REF 195-5…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0782-2020·2020-01-15

    Siemens Cios Alpha Mobile X-Ray System Recalled for C-Arm Holder Crack

    Siemens Medical Solutions is recalling Cios Alpha mobile X-ray systems because a crack in the C-arm holder could compromise stability and lead to injury.

    Product
    Cios Alpha, Model Number 10308191; mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical application
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0787-2020·2020-01-15

    Intersurgical Airway Connector Recalled for Potential Swivel Elbow Cracking

    Intersurgical Inc is recalling 50,400 airway connectors because the swivel elbow port may crack and leak. The recall covers products distributed nationwide in the US.

    Product
    Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3521000. Airway connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0781-2020·2020-01-15

    Stryker Pin To Rod Coupling Recalled for Clamping Failure

    Stryker is recalling Pin To Rod Couplings for the Hoffmann II Compact External Fixation System because they may fail to clamp the pin and rod as intended.

    Product
    Stryker Pin To Rod Coupling External Fixation System Hoffmann II Compact - Pin To Rod Coupling 5/3-4mm Catalog #: 4940-1-020 - Product Usage: Indications Distal radius fractures (intra and extra) articular Intercarpal fracture dislocations Unstable forearm fractures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0786-2020·2020-01-15

    Intersurgical Airway Connector Recalled for Potential Swivel Elbow Cracking

    Intersurgical Inc is recalling 19,200 airway connectors because the swivel elbow port may crack and leak.

    Product
    Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airway connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0783-2020·2020-01-15

    Abbott Fast-Cath Trio Hemostasis Introducer Recalled for Incorrect Size

    Abbott Medical is recalling 814 Fast-Cath Trio Hemostasis Introducer devices because they contain 12F components instead of the expected 14F size.

    Product
    Fast-Cath Trio HEMOSTASIS INTRODUCER, 14F, 4.6 mm, REF 406303
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0464-2020·2020-01-15

    Wayfare Vanilla Pudding Recalled for Package Bloating and Off Flavors

    Wayfare Health Foods LLC is recalling Plant Based Vanilla Pudding due to consumer complaints about package bloating, sourness, and textural issues.

    Product
    Plant Based WayFare Vanilla Pudding Organic Dairy Free, Item #1221. Net wt. 4 oz. There are 4/4 oz. cups per pack with cardboard overwrap. UPC 845681000358.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0785-2020·2020-01-15

    SURE Anti-Perspirant Recalled for Undeclared Active Ingredient Labeling Error

    Idelle Labs is recalling SURE 48hr Confidence Anti-Perspirant because the label lists an active ingredient that is not actually in the product.

    Product
    SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5514-1 UPC 8 83484 717936 6 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0463-2020·2020-01-15

    Wayfare Chocolate Pudding Recalled for Packaging and Flavor Issues

    Wayfare Health Foods LLC is recalling Plant Based WayFare Chocolate Pudding due to consumer complaints about bloated packaging, off flavors, and textural changes.

    Product
    Plant Based WayFare Chocolate Pudding Organic Dairy Free, Item #1222. Net wt. 4 oz. There are 4/4 oz. cups per pack with cardboard overwrap. UPC 845681000365.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0792-2020·2020-01-15

    Cochlear Baha 5 Sound Processor Battery Door Recall

    Cochlear Americas Inc. is recalling 50 units of Baha 5 Sound Processor Tamper Proof Battery Doors packaged with the incorrect component.

    Product
    Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.)
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0776-2020·2020-01-15

    Nextremity Solutions Recalls Stratum MDS Screws Due to Length Discrepancy

    Nextremity Solutions is recalling 87 Stratum MDS Screws because they are 2mm shorter than the length indicated on the package label.

    Product
    Stratum MDS Screw 3.5x46mm ST Part Number: STRM-MDS-3546ST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0559-2020·2020-01-15

    Grey Ghost Bakery Lemon Sugar Cookies Recalled for Undeclared Sulfites

    Grey Ghost Bakery is recalling Lemon Sugar cookies in various sizes due to undeclared sulfites. The product was distributed to numerous states across the US.

    Product
    GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152 00332 6 & 8 OZ (225 G) UPC 8 53152 00307 4 GREY GHOST BAKERY 1750 SIGNAL POINT RD, STE 2A CHARLESTON, SC 29412
    Category
    Food
    Distribution
    41 states
  • ModerateFDA (Devices)·Z-0777-2020·2020-01-15

    Nextremity Solutions Recalls Stratum MDS Screws Due to Length Discrepancy

    Nextremity Solutions is recalling 86 Stratum MDS Screws because the components are 2mm shorter than indicated on the package label.

    Product
    Stratum MDS Screw 3.5x48mm ST Part Number: STRM-MDS-3548ST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0779-2020·2020-01-15

    Medical Action Industries Recalls Medical Convenience Kits Due to Saline pH Defect

    Medical Action Industries is recalling 9,924 cases of medical convenience kits because the included saline solution may exceed USP pH requirements.

    Product
    Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit, REF 77070B ***DIALYSIS*** Clear Sequence Change Kit, REF 77068B ***PEDS CVC*** Clear Sequence Change Kit, REF 77190B ***PICC*** Clear Sequence Change Kit…
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Drugs)·D-0783-2020·2020-01-15

    Idelle Labs Recalls SURE 48 hr Anti-Perspirant for Labeling Error

    Idelle Labs is recalling SURE 48 hr Confidence Unscented Anti-Perspirant & Deodorant because the label lists an active ingredient that is not actually in the product.

    Product
    SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g) NDC# 41595-5509-2 UPC 8 83484 71717 2 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0778-2020·2020-01-15

    Nextremity Solutions Recalls Stratum MDS Screws Due to Length Discrepancy

    Nextremity Solutions is recalling 86 Stratum MDS Screws because they are 2mm shorter than the length indicated on the package label.

    Product
    Stratum MDS Screw 3.5x50mm ST Part Number: STRM-MDS-3550ST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0638-2020·2020-01-15

    Lupin Recalls Blisovi Fe 1.5/30 Tablets Due to Crumbling

    Lupin Pharmaceuticals is recalling Blisovi Fe 1.5/30 tablets because they crumble when removed from the blister pack.

    Product
    Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP and ferrous fumarate tablets 75mg), Rx Only, Distributed by: Lupin Pharmaceuticals Inc Baltimore, MD 21202, Manufactured for: Lupin Limited Pithampur 454775 INDIA 240875, NDC 68180-866-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0465-2020·2020-01-15

    Wayfare Butterscotch Pudding Recalled for Package Bloating and Off Flavors

    Wayfare Health Foods LLC is recalling Plant Based Butterscotch Pudding due to consumer complaints of package bloating, off flavors, and textural issues.

    Product
    Plant Based WayFare Butterscotch Pudding Organic Dairy Free, Item #1223. Net wt. 4 oz. There are 4/4 oz. cups per pack with cardboard overwrap. UPC 845681000372.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0794-2020·2020-01-15

    Baxter Recalls One-Link Needle-Free IV Connectors Due to Connection Force Issue

    Baxter Healthcare is recalling One-Link Needle-Free IV Connectors because some units require higher-than-expected force to connect securely to standard Luer adapters.

    Product
    ONE-LINK Needle-free IV Connector, Product Codes: 7N8300, 7N8301, 7N8310, 7N8330K, 7N8332K, 7N8334K, 7N8370K, 7N8371, 7N8375K, 7N8376K, 7N8377, 7N8378, 7N8390, 7N8391, 7N8399 - Product Usage: intended for single patient use with a vascular access device for the administration of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0786-2020·2020-01-15

    Idelle Labs Recalls SURE 48hr Anti-Perspirant Due to Labeling Error

    Idelle Labs is recalling SURE 48hr Confidence Unscented Anti-Perspirant because the label lists an active ingredient that is not actually in the product.

    Product
    SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5513-2 UPC 8 83484 71794 3 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0784-2020·2020-01-15

    Idelle Labs Recalls SURE Antiperspirant for Undeclared Active Ingredient

    Idelle Labs is recalling SURE 48hr Confidence Nourishing Coconut Antiperspirant & Deodorant because the label lists an active ingredient that is not actually in the product.

    Product
    SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant & Deodorant Net Wt 2.6 oz (73g) NDC# 41595-5547-1 UPC 8 83484 31020 5 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·20056·2020-01-14

    Thompson's WaterSeal Aerosol Protectors Recalled for Fire Hazard

    The Thompson's Company is recalling about 852,000 aerosol cans of WaterSeal wood and masonry protectors because leaking propellant poses a fire hazard.

    Product
    Thompson's® WaterSeal® Waterproofing Wood Protector and Masonry Protector in Aerosol Cans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V012000·2020-01-13

    Toyota and Lexus Recall Vehicles for Fuel Pump Failure Risk

    Toyota is recalling approximately 1.8 million vehicles because a fuel pump failure could cause the engine to stall while driving, increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA RC 350, CAMRY, ES350, RC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide