The Recall Desk

State

Alaska product recalls

72,820 recalls have nationwide distribution and so reach Alaska. 1,763 additional recalls listed Alaska specifically in their distribution scope.

What the numbers show

Total
1,763
Critical
118
Severe
349
Most recent
2026-09-02

Of the 1,763 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 349 (20%) are Severe.

Which agencies issued them

These figures cover only the 1,763 recalls whose distribution notice names Alaska specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

251–275 of 74583

  • HighFDA (Devices)·Z-2945-2026·2026-08-19

    Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges

    Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.

    Product
    Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog Number: PE13SPAJB; 4) KIT, SINUS , Catalog Number: PE13SPAJC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2935-2026·2026-08-19

    Straumann BLT Dental Implant Recall Due to Incorrect Length Labeling

    Straumann USA LLC is recalling 175 units of BLT dental implants that may be 12mm instead of the labeled 14mm length.

    Product
    Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant, endosseous, root-form
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2927-2026·2026-08-19

    Remel Neisseria meningitidis Gp C In Vitro Diagnostics Recall

    Remel Europe Ltd. is recalling specific lots of Neisseria meningitidis Gp C in vitro diagnostics that fail to meet performance criteria.

    Product
    Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2915-2026·2026-08-19

    GORE VIABIL Biliary Endoprosthesis Recalled for Incorrect Labeling

    W L Gore & Associates is recalling 13 GORE VIABIL Short Wire Biliary Endoprostheses because they were incorrectly labeled with the wrong model number and dimensions.

    Product
    GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1006. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common bile duct which may be obstructed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2916-2026·2026-08-19

    Spacelabs Xhibit Central Station Recalled for DisplayPort Audio/Video Failures

    Spacelabs Healthcare is recalling 6,074 Xhibit Central Station units because an off-the-shelf DisplayPort audio/video splitter component may fail.

    Product
    Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product Description: The Spacelabs Healthcare (Spacelabs) Xhibit Central Station, Model 96102. Xhibit offers remote surveillance of patient data for those patients connec
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2930-2026·2026-08-19

    Terumo Glidesheath Slender A-Kit Recalled for Incorrect Guidewire Packaging

    Terumo Medical Corporation is recalling 7,490 units of Glidesheath Slender A-Kits because they were packaged with a 0.025 guidewire instead of the specified 0.021 guidewire.

    Product
    GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2942-2026·2026-08-19

    Procedure kits with MEDICOM Ritmed Neurological Sponges are recalled due to endotoxin variability.

    The FDA is recalling procedure kits containing MEDICOM Ritmed Neurological Sponges because of unexpected variability in endotoxin levels. This affects consumers who have received or plan to receive these kits.

    Product
    Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT , Catalog Number: 21-4720B; 2) TRAY FAT GRAFT ADD , Catalog Number: 21-4720C; 3) KIT,BOSC MICROLARYNGOSCOPY , Catalog Number: PECGMLBOB; 4) KIT,ASLMC NASAL PACK , Catalog Number: PECGNAAU8;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2917-2026·2026-08-19

    Galt Medical Recalls Boston Scientific Transcarotid Access Kits

    Galt Medical Corporation is recalling 114,260 Boston Scientific Enhance Transcarotid/Peripheral Access Kits because black depth markings may detach from the outer sheath.

    Product
    Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator , Stiffen Dilator, Nitinol Mandrel Wire w/ Radiopaque Tip [Au}, Needle, Extension Tube with Stopcock
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0760-2026·2026-08-19

    Shoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations

    Shoolin Pharma Chem LLP is recalling Tadalafil USP 0.100 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.

    Product
    TADALAFIL USP, 0.100 KG, 0.1KG(100gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, Gujarat, 382715, India, (CAS NO 1715996-29-5), NDC 85702-002-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2929-2026·2026-08-19

    Straumann Recalls GM Helix Dental Implants Due to Labeling Mismatch

    Straumann USA LLC is recalling 417 GM Helix dental implants because the implant inside the packaging may not match the outer carton label, potentially causing installation issues.

    Product
    GM Helix Implant, Endosseous Dental Implant Article No. 109.984
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2913-2026·2026-08-19

    Ventana Recalls navify Digital Pathology Software Due to Image Metadata Discrepancies

    Ventana Medical Systems is recalling navify Digital Pathology software versions 2.5 due to reported discrepancies between images and metadata in the viewer.

    Product
    navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material Number 09453733001 UDI-DI Code: 761333602095AQ In the United States, navify Digital Pathology software (previously known as uPath Enterprise Software) i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0768-2026·2026-08-19

    Heritage Pharmaceuticals Recalls Clindamycin Palmitate Hydrochloride Due to Foreign Particles

    Heritage Pharmaceuticals is recalling Clindamycin Palmitate Hydrochloride oral solution due to the presence of particles and white flakes in reconstituted bottles.

    Product
    CLINDAMYCIN PALMITATE HYDROCHLORIDE — CLINDAMYCIN PALMITATE HYDROCHLORIDE (CLINDAMYCIN PALMITATE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0759-2026·2026-08-19

    Sildenafil Citrate USP Recalled for CGMP Deviations Noted During FDA Inspection

    Shoolin Pharma Chem LLP is recalling Sildenafil Citrate USP due to Current Good Manufacturing Practice (CGMP) deviations identified during an FDA inspection.

    Product
    SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesana, Gujarat, 382715, India, (CAS NO. 171599-83-0) NDC 85702-001-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2914-2026·2026-08-19

    GORE VIABIL Biliary Endoprosthesis Recalled for Incorrect Labeling

    W L Gore & Associates is recalling 13 GORE VIABIL Short Wire Biliary Endoprostheses because they were incorrectly labeled with the wrong model number and dimensions.

    Product
    GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1010. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common bile duct which may be obstructed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0763-2026·2026-08-19

    Sildenafil Citrate Recall Due to CGMP Deviations

    Shoolin Pharma Chem LLP is recalling Sildenafil Citrate USP 1.00KG bags due to CGMP deviations noted during an FDA inspection.

    Product
    SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, Gujarat, 382715, India, (CAS NO. 171599-83-0) NDC 85702-001-08.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V534000·2026-08-17

    Terex Digger Derrick Trucks Recalled for Weld Defect

    Ring Power is recalling 2019-2026 Terex digger derrick trucks because a weld defect may cause the pole guide arm to fall, risking injury.

    Product
    TEREX — TEREX C5000, C6000, GENERAL 65, C4000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E058000·2026-08-17

    Holley Recalls Replacement Carburetors and Throttle Body Kits

    Holley Performance Products is recalling certain replacement carburetors and throttle body kits because undersized levers may cause a loss of throttle control.

    Product
    FUEL SYSTEM, GASOLINE:CARBURETOR SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V535000·2026-08-17

    Heil Recalls Front Loader Garbage Trucks Due to CNG Ladder Bolt Defect

    Heil is recalling 2016-2026 front loader garbage trucks with specific CNG ladder kits because an incorrect bolt may damage CNG cylinders, increasing fire risk.

    Product
    HEIL — HEIL FRONT END LOADER GARBAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·017-2026·2026-08-17

    Gangothri Foods Recalls Uninspected Ready-to-Eat Pickled Goat and Chicken Products

    Indus Foods, LLC is recalling approximately 1,626 pounds of ready-to-eat pickled goat and chicken products produced without USDA inspection.

    Product
    Indus Foods, LLC DBA Gangothri Foods Recalls Ready-To-Eat Pickled Goat and Chicken Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E057000·2026-08-17

    Heil Recalls CNG Tailgate Ladder Kits Due to Fire Risk

    The Heil Co. is recalling CNG tailgate ladder kits where an incorrect bolt may damage fuel cylinders, increasing fire risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V533000·2026-08-14

    Halcore Recalls 2025-2026 Horton Ambulances Due to Touchscreen Failure

    Halcore Group is recalling 2025-2026 Horton ambulances because touchscreen failures may prevent emergency lights from activating, increasing crash risk.

    Product
    HORTON — HORTON TYPE I, TYPE III, CRITICAL CARE TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26688·2026-08-13

    Taleco Gear Recalls Baby Jumpers and Swings Over Fall and Strangulation Hazards

    Taleco Gear is recalling about 41,100 baby jumpers, baby swings and 2-in-1 baby jumper and swings due to risks of falls, impacts and strangulation. The products can become unstable and the hanging restraint straps and seat openings pose strangulation hazards.

    Product
    G Taleco Gear Baby Jumpers, Baby Swings and 2-in-1 Baby Jumper & Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26694·2026-08-13

    Merax Murphy Beds Recalled Due to Risk of Serious Injury or Death

    GigaCloud Technology is recalling Merax full-size and twin-size Murphy beds because the frames can fall during assembly or disassembly, posing impact and crush hazards.

    Product
    Merax Full-Size and Twin-Size Murphy Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide