The Recall Desk

State

Alaska product recalls

72,907 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.

Which agencies issued them

These figures cover only the 1,764 recalls whose distribution notice names Alaska specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1301–1325 of 74671

  • HighFDA (Devices)·Z-2351-2026·2026-06-17

    MIC Safety 20 Fr PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits with ENFit Connectors, 20 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues. 6,005 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2356-2026·2026-06-17

    NexxZr dental zirconia discs may have reduced or missing dentin layer

    NexxZr T Multi A3.5 zirconia discs for all-ceramic dental restorations are being recalled because a reduced or missing dentin layer increases the risk of fracture in the mouth.

    Product
    NexxZr T Multi A3.5 W98-16mm, REF: 745451
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2413-2026·2026-06-17

    Orca single use endoscope valves recalled over sticking suction buttons

    Boston Scientific is removing Orca Sterile, Single Use Air/Water and Suction Valves because of a higher than anticipated occurrence of the suction button sticking. 9,750 units affected.

    Product
    Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2405-2026·2026-06-17

    Abbott Merlin pacemaker programmer may fail to terminate threshold test

    Merlin Patient Care System programmer software is being recalled because a malfunction during a pacing capture threshold test may stop the command to terminate the test being communicated.

    Product
    Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2312-2026·2026-06-17

    Plum Duo infusion pumps may not display soft limit alerts

    Plum Duo Infusion Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.

    Product
    Plum Duo Infusion Pump, 40002-0401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2347-2026·2026-06-17

    MIC Safety 14 Fr push PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits with ENFit Connectors, 14 Fr PUSH OTW, catalog number 8170-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2407-2026·2026-06-17

    Halyard pain packs shipped without validated sterilization in Iowa

    Halyard Pain Packs, kit code AMPK48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 120 kits affected.

    Product
    Halyard, Pain Pack. Kit Code: AMPK48-01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2335-2026·2026-06-17

    CORFLO Safety PEG kit 30-6312 contains recalled lidocaine injection

    CORFLO Safety PEG Kits, catalog number 30-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 31 kits are affected.

    Product
    Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2408-2026·2026-06-17

    Halyard towel six packs shipped without validated sterilization in Iowa

    Halyard Towel Six Packs, kit code AMTS70-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 224 kits affected.

    Product
    Halyard, Towel Six Pack. Kit Code: AMTS70-01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2406-2026·2026-06-17

    MOSAIQ oncology software may fail to load adapted treatment plan

    The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.

    Product
    MOSAIQ Oncology Information System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2346-2026·2026-06-17

    MIC Safety 24 Fr pull PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits, 24 Fr PULL, catalog number 7180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 1,006 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2336-2026·2026-06-17

    CORFLO Safety PEG kit 30-6316 contains recalled lidocaine injection

    CORFLO Safety PEG Kits, catalog number 30-6316, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 41 kits are affected.

    Product
    Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2361-2026·2026-06-17

    Medartis APTUS compression screws have off-centre cannulation in affected lots

    Medartis APTUS 5.0 headed cannulated compression screws for bone fixation are being recalled because the cannulation of the screw is not centered. 13 units are affected.

    Product
    Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0586-2026·2026-06-17

    Zep alcohol sanitizer spray drums recalled for microbial contamination

    Zep Alcohol Sanitizer Spray, ethanol 70%, in 55-gallon drums is being recalled for microbial contamination. Five drums are affected.

    Product
    Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by: Zap Inc., 350 Joe Frank Harris Parkway, SE, Emerson, GA 30137, NDC 66949-133-85.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2348-2026·2026-06-17

    MIC Safety 20 Fr push OTW PEG kits contain recalled lidocaine

    MIC Safety PEG Kits with ENFit Connectors, 20 Fr PUSH OTW, catalog number 8170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2400-2026·2026-06-17

    Aluminum chloride hemostatic gel kits shipped with wrong package insert

    Advance Aluminum Chloride Gel Clear Hemostatic Gel Kits are being recalled because some units contain the package insert for Ferric Sulfate Gel, which gives different first aid instructions.

    Product
    Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2399-2026·2026-06-17

    Hintermann left talar implant packaging contained a right-side device

    Hintermann Series Talar Implants, Left, Size 2, are being recalled because packaging and labeling for a left implant contained a right implant device. 67 units are affected.

    Product
    Hintermann Series Talar Implant, Left, Size 2 REF 302112
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2404-2026·2026-06-17

    Boston Scientific Clik X anchors may lack sterility assurance

    Boston Scientific Clik X Anchors, model SC-4318, are being recalled because the sterile anchors may lack sterility assurance. 43 units are affected.

    Product
    Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2329-2026·2026-06-17

    CGuard Prime 10mm by 30mm carotid stents may fail deployment

    CGuard Prime Carotid Stent Systems, 135 cm with a 10 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.

    Product
    CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0607-2026·2026-06-17

    Budesonide inhalation ampules contain black and brown specks and particles

    Budesonide Inhalation Suspension, 1 mg/2 mL single-dose ampules from Sun Pharmaceutical, is being recalled after a quality complaint of black or brown specs and particles in the solution.

    Product
    BUDESONIDE — BUDESONIDE (BUDESONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2362-2026·2026-06-17

    EXENT Analyser marked plates as passed without performing quality control

    An EXENT Analyser is being recalled after plates 2 and 3 were marked as passed although quality control appeared not to have been performed, despite samples being measured.

    Product
    Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2326-2026·2026-06-17

    CGuard Prime 8mm carotid stent systems may resist or fail deployment

    CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 40 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.

    Product
    Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2316-2026·2026-06-17

    GE Allia IGS 7 Pulse systems pose shock risk to servicers

    Allia IGS 7 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. 35 units affected.

    Product
    Allia IGS 7 Pulse angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide