The Recall Desk

State

Indiana product recalls

72,971 recalls have nationwide distribution and so reach Indiana. 9,556 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,556
Critical
1,903
Severe
2,136
Most recent
2026-09-16

Of the 9,556 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,136 (22%) are Severe.

These figures cover only the 9,556 recalls whose distribution notice names Indiana specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6701–6725 of 82527

  • HighFDA (Devices)·Z-1894-2025·2025-06-11

    Signature Laparoscopic Allis Clamp Grasper with Rotating Shaft Recalled

    Silex Medical is recalling the Signature Laparoscopic Instruments Allis Clamp Grasper due to incomplete insulation on the shaft, leaving an exposed area that could pose an electrical hazard during surgical procedures.

    Product
    Signature Laparoscopic Instruments, Allis Clamp Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862030.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1895-2025·2025-06-11

    Signature Laparoscopic Debakey Grasper Instruments Recalled for Insulation Defect

    Silex Medical is recalling 8 units of Signature Laparoscopic Debakey Grasper instruments (Model 5862100) due to incomplete insulation on the shaft near the rotator wheel, which could expose the user or patient to electrical contact.

    Product
    Signature Laparoscopic Instruments, Debakey Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862100.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1885-2025·2025-06-11

    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack Recalled

    Mozarc Medical US LLC is recalling Palindrome Precision Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. Affected units were distributed worldwide including the US, Canada, and Mexico.

    Product
    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1903-2025·2025-06-11

    Luminex VERIGENE Gram Negative Blood Culture Test Recalled

    Luminex is recalling VERIGENE Gram Negative Blood Culture test cartridges due to a consumable issue that may produce incorrect results on a small portion of one lot.

    Product
    VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results VERIGENE System; invitro diagnostic test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2025·2025-06-11

    MAHURKAR Chronic Hemodialysis Catheter recalled for sterile barrier defect

    Mozarc Medical is recalling MAHURKAR Chronic Hemodialysis Catheter Sport Pack units due to a potential breach in sterile barrier packaging that could compromise the product's sterility.

    Product
    MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0928-2025·2025-06-11

    GNC Women's 30+ Vitapak recalled due to undeclared fish allergen

    GNC Holdings LLC is recalling GNC Women's 30+ Vitapak due to undeclared fish allergen (parvalbumin). The product was distributed across multiple states.

    Product
    GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that measures 10.25 width x 3.56 height x 3.15 depth containing 30 sachets of 3 width x 2.75 height with tear notch. 15 Cartons per Case
    Category
    Food
    Distribution
    48 states
  • HighNHTSA·25V368000·2025-06-11

    Nova Bus turn signal indicator lights may remain solidly illuminated

    Nova Bus is recalling certain 2022-2023 LFS buses because a digital display firmware error may leave the instrument panel turn signal indicators solidly lit, failing FMVSS 108.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1908-2025·2025-06-11

    Beckman Coulter Sample Probes with Defective Tips Clinical Chemistry

    Beckman Coulter is recalling sample probes with defective tips used in clinical chemistry analyzers. The defective probes may dispense lower sample concentrations, potentially leading to false low test results and delayed diagnosis.

    Product
    Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V365000·2025-06-11

    Mercedes-Benz Recalls 2023 GLC 300 Models for Missing Headlight Caps

    Mercedes-Benz is recalling 2023 GLC 300 and GLC 300 4MATIC vehicles because missing caps allow improper headlight adjustment, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300, GLC 300 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1906-2025·2025-06-11

    Dexcom G7 iOS App version 2.7.0 stops updating glucose readings

    Dexcom G7 iOS App version 2.7.0 can enter a state where glucose readings freeze and alerts do not trigger, risking missed detection of dangerously high or low blood sugar. Other connected devices like Apple Watch and insulin pumps continue to receive glucose data directly from the transmitter.

    Product
    Dexcom G7 iOS Application, Ref: SW12300 used in conjunction with the Dexcom G7 Continuous Glucose Monitoring (CGM) system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V387000·2025-06-11

    Rivian R1S and R1T front turn signals may fail to illuminate

    Rivian is recalling certain 2025 R1S and R1T vehicles because one or both front turn signals may fail to illuminate and flash, failing FMVSS 108. 27,882 units affected.

    Product
    RIVIAN — RIVIAN R1S, R1T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1897-2025·2025-06-11

    Signature Laparoscopic Bullet Tip Grasper Instrument Insulation Defect Recall

    Silex Medical is recalling 6 units of the Signature Laparoscopic Bullet Tip Grasper with Rotating Shaft due to incomplete insulation on the shaft near the rotator wheel, which could expose users to electrical hazards.

    Product
    Signature Laparoscopic Instruments, Bullet Tip Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863030.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1900-2025·2025-06-11

    Signature Laparoscopic Atraumatic Grasper Insulation Defect Recall

    Silex Medical is recalling Signature Laparoscopic Instruments (Model 5881033) because insulation on the shaft does not fully extend to the proximal end, leaving an exposed area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, 20mm Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5881033.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1899-2025·2025-06-11

    Signature Laparoscopic Atraumatic Grasper Instrument Insulation Defect Recall

    Silex Medical is recalling Signature Laparoscopic Atraumatic Grasper instruments (Model 5864000) due to incomplete insulation on the shaft that leaves an exposed area near the rotator wheel, posing an electrical safety risk during surgical use.

    Product
    Signature Laparoscopic Instruments, Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5864000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1886-2025·2025-06-11

    Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack Recalled

    Mozarc Medical is recalling Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Packs due to a potential breach of sterile barrier packaging that could compromise the catheter's sterility.

    Product
    Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1911-2025·2025-06-11

    Olympus EVIS EXERA III Duodenovideoscope TJF-Q190V Contamination Risk

    Olympus is recalling the EVIS EXERA III Duodenovideoscope Model TJF-Q190V due to post-market data showing higher microbial contamination when manual cleaning is delayed beyond one hour after patient use.

    Product
    Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1898-2025·2025-06-11

    Signature Laparoscopic Alligator Grasper Instrument Recall Safety Issue

    Silex Medical is recalling the Signature Laparoscopic Alligator Grasper with Rotating Shaft (Model 5863050) because insulation on the tube does not fully extend to the proximal end of the shaft, leaving an exposed uninsulated area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, Alligator Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863050.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1888-2025·2025-06-11

    Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack recalled

    Mozarc Medical is recalling Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. The affected catheter models were distributed nationwide in the US and in Canada and Mexico.

    Product
    Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0455-2025·2025-06-11

    Fluoxetine Tablets USP 20 mg Recalled for N-Nitroso Contamination

    Torrent Pharma Inc. is recalling Fluoxetine Tablets USP 20 mg due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit. The affected lot is distributed nationwide.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1887-2025·2025-06-11

    Palindrome Precision SI Chronic Hemodialysis Catheter Sterile Barrier Recall

    Mozarc Medical US LLC is recalling Palindrome Precision SI Chronic Hemodialysis Catheters (Sport Pack) due to a potential breach of sterile barrier packaging. Approximately 95,938 units distributed nationwide and in Canada and Mexico are affected.

    Product
    Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1893-2025·2025-06-11

    Signature Laparoscopic Dolphin Nose Grasper Instrument Insulation Defect

    Silex Medical is recalling 2 units of a Signature Laparoscopic Instruments Dolphin Nose Grasper with Rotating Shaft due to incomplete insulation on the shaft, leaving an exposed area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, Dolphin Nose Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5860020.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1913-2025·2025-06-11

    DxI 9000 Access Immunoassay Analyzer Software Update Error Codes

    Beckman Coulter is recalling DxI 9000 Access Immunoassay Analyzers running software version 1.20 because the update introduces error codes that prevent assays from being performed and may delay result generation.

    Product
    DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software version 1.20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0457-2025·2025-06-11

    Lacosamide Oral Solution recalled for defective leaking containers

    Apotex Corp. is recalling Lacosamide Oral Solution because certain bottles may leak when stored horizontally. Patients taking this seizure medication should contact their pharmacy or healthcare provider.

    Product
    Lacosamide Oral Solution, USP, 10 mg/mL, 200 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston FL 33326, NDC 60505-0405-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0454-2025·2025-06-11

    Indomethacin Extended-Release Capsules recalled for cGMP deviations

    Amerisource Health Services LLC is recalling Indomethacin Extended-Release Capsules 75 mg due to cGMP (current Good Manufacturing Practice) deviations. The recall affects 21 cartons distributed nationwide.

    Product
    INDOMETHACIN — INDOMETHACIN (INDOMETHACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1891-2025·2025-06-11

    FoundationOne Companion Diagnostic F1CDx Incorrect Claim Display

    Foundation Medicine is recalling the FoundationOne Companion Diagnostic (F1CDx) due to an incorrect negative claim displayed on the claims page, though device variant information was correctly shown in the tumor profiling section of the approved test report.

    Product
    FoundationOne Companion Diagnostic (F1CDx)
    Category
    Medical Device
    Distribution
    Distributed nationwide