The Recall Desk

State

Alaska product recalls

72,982 recalls have nationwide distribution and so reach Alaska. 1,764 additional recalls listed Alaska specifically in their distribution scope.

What the numbers show

Total
1,764
Critical
118
Severe
350
Most recent
2026-09-09

Of the 1,764 recalls naming Alaska we have scored against our rubric, 118 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 350 (20%) are Severe.

These figures cover only the 1,764 recalls whose distribution notice names Alaska specifically. The 72,982 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6376–6400 of 74746

  • 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-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-1910-2025·2025-06-11

    ChannelCheck Convenience Pack Pre-filled Water Syringes Recalled

    Healthmark Industries is recalling ChannelCheck Convenience Pack Pre-filled Water Syringes (Models UCC-222CP and UCC-222-ESP) because contamination was found in duodenoscope samples linked to the syringes, which were improperly used outside their intended purpose.

    Product
    ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1896-2025·2025-06-11

    Signature Laparoscopic Sharp Tooth Grasper Insulation Defect Recall

    Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.

    Product
    Signature Laparoscopic Instruments, Sharp Tooth Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863020.
    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 (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
  • 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-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
  • 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-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-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
  • ModerateFDA (Devices)·Z-1907-2025·2025-06-11

    Beckman Coulter Sample Probe Manufacturing Defect Recall

    Beckman Coulter Mishima is recalling sample probes due to a manufacturing defect where rounded and chamfered corners prevent proper air layer formation, causing sample dilution and inaccurate test results.

    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
  • 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
  • ModerateFDA (Devices)·Z-1909-2025·2025-06-11

    Pre-filled Water Syringe recalled for improper use contamination

    Healthmark Industries is recalling Pre-filled Water Syringes (Model SW-010-100 and SW-010) after duodenoscope contamination was linked to improper use of the syringes outside their intended purpose.

    Product
    Pre-filled Water Syringe, Model Numbers SW-010-100 and SW-010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1890-2025·2025-06-11

    FoundationOne Companion Diagnostic contains incorrect negative claims

    Foundation Medicine is recalling two FoundationOne Companion Diagnostic (F1CDx) test reports that contained an incorrect negative claim on the claims page, though the device variant information displayed correctly in the tumor profiling section.

    Product
    FoundationOne Companion Diagnostic (F1CDx)
    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-0458-2025·2025-06-11

    Hand Sanitizer Recalled for Subpotent Ethyl Alcohol Content

    Spectrum Advanced Gel Hand Sanitizer (70% ethyl alcohol, 8 FL OZ) has been recalled nationwide because affected batches contain cloudy appearance and test below the claimed 70% alcohol concentration, making them less effective.

    Product
    HAND SANITIZER — HAND SANITIZER (ETHYL ALCOHOL)
    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-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
  • LowFDA (Food)·F-0840-2025·2025-06-11

    Nordic Naturals Zero Sugar Kids Multivitamin Gummies Recall

    Nordic Naturals is recalling Zero Sugar Kids Multivitamin Supplement gummies due to product mislabeling. Consumers should stop using the product and contact the manufacturer with questions.

    Product
    Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case
    Category
    Consumer Product
    Distribution
    20 states
  • HighNHTSA·25V331000·2025-06-10

    Hyundai Translead Recalls 2026 Dry Van Trailers for Liftgate Pin Defect

    Hyundai Translead is recalling 2026 Dry Van Trailers because insufficient lubrication on the liftgate cylinder pin may cause it to seize, leading to liftgate failure and injury risk.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DRY VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V364000·2025-06-10

    Forest River trailer side gate latches may unlock during transit

    Forest River is recalling certain 2025 Salem and Wildwood travel trailers because the side entry gate latch may unlock, allowing the strut to open the gate during transit.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide