The Recall Desk

State

Indiana product recalls

73,566 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
1,913
Severe
2,529
Most recent
2026-10-24

Of the 9,592 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 2,529 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27026–27050 of 83158

  • HighFDA (Food)·F-0744-2021·2021-07-07

    JUST Egg Sous Vide Plant Egg Bites Recalled for Undeclared Egg and Milk

    Cuisine Solutions is recalling JUST Egg Inspired by Mexico Roasted Poblanos Sous Vide Plant Egg Bites nationwide due to undeclared egg and milk allergens. Consumers with allergies to egg or milk who purchased these products should not consume them.

    Product
    JUST Egg Inspired by Mexico Roasted Poblanos, Ancho Chilli Powder, Black Beans, Corn, Lime 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402517, Expiration dates 3/3/2022, 3/29/2022, 3/10/2022, and 4/7/2022. 16 cartons per corrugated case, Carton GTIN 7 05044 02517 9…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1955-2021·2021-07-07

    Synaptive Suction Sets Recalled for Metal Burrs on Tube Interior

    Synaptive Medical is recalling 1,291 Trackable Suction Sets for visible metal burrs and filings along the inner suction tube. The defect may contaminate the surgical field or cause injury.

    Product
    Synaptive Trackable Suction Set Standard and Malleable
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Devices)·Z-1975-2021·2021-07-07

    PERLA TL Lateral Connector Open Spinal Fusion Devices Recalled for External Label Error

    SPINEART SA is recalling 44 units of PERLA TL Lateral Connector Open spinal fusion connectors distributed in the U.S. due to external labels that incorrectly list the rod size.

    Product
    PERLA TL Lateral Connector Open - Product Usage: intended to be used with autograft and/or allograft. Pediatric pedicle screw fixation is limited to a posterior approach. Models: PERLA TL Lateral Connector Open, 15mm PERLA TL Lateral Connector Open, 30mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1979-2021·2021-07-07

    Philips CT Monitor Bracket Assembly risks ceiling fall hazard

    Philips is recalling 1,301 Monitor Bracket Assemblies used in CT and PET/CT imaging systems worldwide due to potential shaft wear that could cause the monitor to detach from the ceiling mount and fall, posing injury risk.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and PET/CT systems: Model - MX8000 Models: 728120/728125/728201
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1964-2021·2021-07-07

    Edwards TruWave Pressure Monitoring Set Recalled for Potential Tubing Detachment

    Edwards Lifesciences is recalling 990 units of the Edwards TruWave (30 cc)/VAMP Jr Kit pressure monitoring set because the pressure tubing may detach from the blood sampling system. Healthcare facilities should discontinue use.

    Product
    Edwards TruWave (30 cc)/VAMP Jr Kit, REF: VMP306PX, Pressure Monitoring Set, Rx Only, CE, UDI: (01)57460691950370
    Category
    Medical Device
    Distribution
    33 states
  • HighFDA (Devices)·Z-1984-2021·2021-07-07

    Philips CT Monitor Bracket Assembly May Detach and Fall

    Philips is recalling 1,301 monitor bracket assemblies for CT imaging systems due to shaft wear that could cause detachment and fall of the monitor. This could result in serious injury to patients, operators, and staff.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Ingenuity Core, Ingenuity Core 128, Ingenuity CT 728321 - Ingenuity Core 728323 - Ingenuity Core 128 728326/728327 - Ingenuity CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1976-2021·2021-07-07

    Medtronic Endurant II Stent Graft System Recalled for Incorrect Assembly

    Medtronic is recalling 3 Endurant II/IIs Stent Graft Systems due to an incorrect stentstop assembly component in the delivery system. The defective devices use an 18-French assembly instead of the required 20-French component.

    Product
    Endurant II/IIs Stent Graft System: STENT GRAFT ETBF3216C145E ENDUR II BIF. For treatment of vascular aneurysms.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1990-2021·2021-07-07

    Monitor Bracket Assembly Shaft Wear Risk in Philips CT Fluoroscopy Systems

    Philips CT fluoroscopy monitor brackets may detach from suspension arms due to unrecognized shaft wear, risking the monitor falling and causing serious injury to patients, operators, or bystanders.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728306 - Brilliance iCT 728311 - Brilliance iCT SP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1965-2021·2021-07-07

    Pressure monitoring set recalled for potential pressure tubing detachment

    Edwards Lifesciences is recalling the TruWave 3 cc/VAMP Jr pressure monitoring set (Lot #63598812) due to a potential risk that the pressure tubing may detach from the blood sampling system.

    Product
    Edwards TruWave 3 cc/VAMP Jr Kit, REF: VMP426PX, Pressure Monitoring Set, Rx Only, CE UDI: (01)57460691950547
    Category
    Medical Device
    Distribution
    33 states
  • HighFDA (Devices)·Z-1983-2021·2021-07-07

    CT Monitor Bracket Assembly Recalled Due to Shaft Wear and Detachment Risk

    Philips North America is recalling CT system monitor bracket assemblies due to shaft wear that could cause the bracket to detach from the suspension arm, potentially allowing the monitor to fall and cause serious injury.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and PET/CT systems. BB (Big Bore) Oncology, BB (Big Bore) Radiology: 728242/728243/728244/728272 - Brilliance Big Bore
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1988-2021·2021-07-07

    Philips Monitor Bracket Assembly falls due to shaft wear in medical imaging systems

    Philips monitor bracket assemblies for CT/PET imaging systems may detach due to shaft wear, posing a risk of the monitor falling and causing serious injury to patients, operators, or bystanders.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 882446 - Vereos PET/CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1996-2021·2021-07-07

    Infusion Pump Order Form Discontinued Due to Ambiguous Reuse Instructions

    Flowonix Medical is recalling physician order forms for Prometra infusion pumps due to ambiguous wording that could be misinterpreted as instructions to reuse previously extracted medication, posing an infection risk.

    Product
    Physician Order Form (PL-15400-00, Nov. 2018) distributed to end user used with the following: Prometra Programmable Infusion Pump System: MODEL/CATALOG #(s): Catalog No. US Model GTIN-14 11827 Prometra Programmable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21160·2021-07-07

    Sovereign Athletic Children's Robes Recalled for Flammability Hazard

    One Twenty Clothing Company is recalling Sovereign Athletic-branded children's robes that fail to meet federal flammability standards for sleepwear, posing a burn hazard to children.

    Product
    Children's Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1959-2021·2021-07-07

    Edwards TruWave Pressure Monitoring Set Recalled for Potential Tubing Detachment

    Edwards Lifesciences is recalling its pressure monitoring set due to potential tubing detachment. Approximately 460 units distributed across North America and Europe are affected.

    Product
    Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO, Sterilized using ethylene Oxide, UDI: (01) 57460691954507
    Category
    Medical Device
    Distribution
    33 states
  • HighFDA (Food)·F-0745-2021·2021-07-07

    JUST Egg Plant Egg Bites recalled for undeclared egg and milk

    Cuisine Solutions is recalling JUST Egg Inspired by India Curry, Broccoli, Cauliflower, Coconut Milk, Lemongrass Sous Vide Plant Egg Bites due to undeclared egg and milk allergens. The product was distributed nationwide.

    Product
    JUST Egg Inspired by India Curry, Broccoli, Cauliflower, Coconut Milk, Lemongrass 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402511, Expiration dates 3/5/2022, 3/31/2022, and 4/9/2022.16 cartons per corrugated case, Carton GTIN 7 05044 02511 7 Case Bar Code 10…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V514000·2021-07-07

    Wayfarer Recalls 2017-2021 Recreational Vehicles Due to Valve Stem Defect

    Wayfarer is recalling 2017-2021 recreational vehicles because valve stem extenders may rub against wheel liners, potentially causing sudden tire pressure loss and increasing crash risk.

    Product
    WAYFARER — WAYFARER WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1977-2021·2021-07-07

    Exactech Humeral Augmented Tray orthopedic implant components recalled for disengagement risk

    Exactech is recalling Humeral Augmented Tray (HAT) orthopedic implant components because the retaining ring may disengage during use. The recall affects 36 devices distributed in six U.S. states.

    Product
    Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT. Each tray contains 1 of each of the following catalog numbers for a total of 6 trials/tray: (1) HAT STD Left Tray Trial, Cat. #321-00-01; (2) HAT STD Right Tray Trial, Cat. #321-00-02; (3) HAT LAT Left…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1962-2021·2021-07-07

    Blood Management System Pressure Tubing May Detach

    Edwards Lifesciences blood management system (VJ0990) pressure tubing may detach from the blood sampling system during use. The recall affects 2,000 units distributed across the U.S., Canada, UK, and Italy.

    Product
    Edwards REF: VJ0990, Blood Management System, Rx Only, Single Use, CE, Sterile EO UDI: (01)57460691951520
    Category
    Medical Device
    Distribution
    33 states
  • HighFDA (Devices)·Z-1961-2021·2021-07-07

    Edwards TruWave Pressure Monitoring Set: Potential Tubing Detachment

    Edwards Lifesciences is recalling a pressure monitoring set due to potential detachment of the pressure tubing from the blood sampling system. The recall affects 290 units distributed across multiple US states and international locations.

    Product
    Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit, REF: T443952B, Pressure Monitoring Set, RX Only, CE, Sterile EO, Sterilized using ethylene Oxide, UDI: (01) 57460691930174 ***Not Marketed within the US
    Category
    Medical Device
    Distribution
    33 states
  • HighFDA (Devices)·Z-1997-2021·2021-07-07

    Tempus Pro Patient Monitor Software Error Risk When Unplugged

    Remote Diagnostic Technologies is recalling Tempus Pro patient monitors (Trizeps 7 variant) that can produce error states when unplugged while connected to a specified laryngoscope device. No injuries have been reported.

    Product
    Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. Part No. - 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. Product Usage: intended to be used as a stand-alone monitor or as a telemedicine system (transmitting patient data to other medical professionals…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1985-2021·2021-07-07

    Monitor Bracket Assembly Wear May Cause Fall Hazard for Medical Imaging Equipment

    Philips medical imaging equipment monitor bracket assemblies may detach due to unrecognized shaft wear, risking the monitor falling and causing serious injury to patients, operators, or bystanders.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728332 - IQon Spectral CT : IQon Spectral CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1994-2021·2021-07-07

    Bard PowerPICC Catheter Kits Recalled for Wrong Guidewire Size

    Bard Access Systems is recalling PowerPICC catheter convenience kits with incorrect guidewires. Kits labeled as containing 70 cm guidewires actually contain 50 cm guidewires, which could affect proper catheter placement.

    Product
    5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire Unit Label: PowerPICC REF CK000340B BARD MYPICC KIT 5F French Size Dual-Lumen 70cm Guidewire
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2021·2021-07-07

    Philips CT Monitor Bracket Assemblies Recalled for Detachment Risk

    Philips has recalled 1,301 Monitor Bracket Assemblies for CT systems worldwide due to shaft wear that could cause monitors to detach and fall, potentially injuring patients, operators, or service personnel.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728333 - Spectral CT:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1989-2021·2021-07-07

    Philips Medical Monitor Bracket May Detach from Ceiling Mount

    Philips medical imaging monitors with worn bracket assembly shafts may detach from ceiling suspensions and fall on patients, operators, or staff. No injuries have been reported.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 882476 - Gemini TF Big Bore PET/CT
    Category
    Medical Device
    Distribution
    Distributed nationwide