State

Alaska product recalls

73,509 recalls have nationwide distribution and so reach Alaska. 1,766 additional recalls listed Alaska specifically in their distribution scope.

What the numbers show

Total: 1,766
Critical: 118
Severe: 470
Most recent: 2026-10-14

Of the 1,766 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 470 (27%) are Severe.

Which agencies issued them

These figures cover only the 1,766 recalls whose distribution notice names Alaska specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25001–25025 of 75275

HighFDA (Devices)·Z-1899-2021·2021-06-23
VENOVO 9F Venous Stent System incomplete deployment and delivery system retention
Bard Peripheral Vascular recalls VENOVO Venous Stent System 9F due to reports that the proximal end fails to expand immediately upon deployment and remains connected to the delivery system.
Product
VENOVO Venous Stent System 9F Product Description(REF)/dimension: VENEL14040 /Venovo 9F 14/40/1200mm OUS; VENEL14060 /Venovo 9F 14/60/1200mm OUS; VENEL14080 /Venovo 9F 14/80/1200mm OUS; VENEL14100 /Venovo 9F 14/100/1200mm OUS; VENEL14120 /Venovo 9F 14/120/1200mm OUS…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1852-2021·2021-06-23
Hydrodissection Cannula Recall Due to Residue at Tip
Anodyne Surgical has recalled hydrodissection cannulas due to a possible yellowish-brown or greenish-brown residue on the tip. The affected devices were distributed in multiple US states and Canada.
Product
Hydrodissection Cannula (Chang), 27g, labeled as: anodynesurgical, REF 7018 ASICO, REF AS-7638 anodynesurgical, REF 7018NS katena, REF K20-3168 anodynesurgical, REF 104910 MSI, REF CA7800 ACCUTONE, REF AX14784-BULK Walcott Rx Products, REF RX2300NS Walcott Rx Products…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1883-2021·2021-06-23
Medtronic Perfusion System Tubing Packs Recalled for Incomplete Welds
Medtronic is recalling 14 tubing packs of its HY10J00R12 perfusion system due to insufficient or incomplete welds. The affected lot is 221227814 with a use-by date of August 28, 2022.
Product
Medtronic HY10J00R12, Custom Pack HY10J00R12 ECC Small CA, Custom Perfusion System,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1873-2021·2021-06-23
Medtronic Perfusion System Tubing Packs Recalled for Incomplete Welds
Medtronic is recalling specific lots of BB10R94R6 Custom Perfusion System tubing packs due to incomplete or insufficient welds. The defect may affect device performance during use.
Product
Medtronic BB10R94R6, Custom Pack BB10R94R6 1/4 ECCPK, Custom Perfusion System, Sterile, Rx.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1874-2021·2021-06-23
Medtronic Perfusion System Tubing Packs Recalled for Incomplete Welds
Medtronic is recalling specific lots of BB11J14R2 Bridge Custom Perfusion System tubing packs due to incomplete or insufficient welds that may have occurred during manufacturing.
Product
Medtronic BB11J14R2, Custom Pack BB11J14R2 Bridge, Custom Perfusion System, Sterile, Rx.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1867-2021·2021-06-23
Mechanical respiratory filter recalls due to sterilization process deviation
Covidien, LP is recalling a mechanical respiratory filter (Item 351/5979) due to potential deviations in ethylene oxide sterilization. The product was distributed worldwide and in multiple U.S. states.
Product
Mechanical Filter with Connector Small, Tethered Cap, Item Code 351/5979 - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1854-2021·2021-06-23
Cardiac Monitoring System Software Error May Disable Device
Abbott's WorkMate Claris cardiac monitoring system (Model H700124) is being recalled due to a software error that may disable the system or turn the screen black. Nine units affected in Michigan, Kansas, Missouri, and Texas.
Product
v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System Display, Model H700124, The WorkMate Claris" System is a computer-based electrocardiographic recording and monitoring system designed for efficient capture, display, and retrieval of surface and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1859-2021·2021-06-23
Dialysate Concentrate for Hemodialysis Recalled for Out-of-Specification Formulation
Medivators, Inc. recalls 1,381 cases of dialysate concentrate due to a manufacturing anomaly that may result in out-of-specification formulation. Affected lots may not function properly in hemodialysis treatment.
Product
Dialysate Concentrate for Hemodialysis-Liquid/Powd - Product Usage: used in conjunction with bicarbonate in a compatible artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V471000·2021-06-23
2020-2021 Nissan vehicles recalled for failed turn signal bulbs
Nissan is recalling certain 2020-2021 Versa, Titan, and Titan XD vehicles because the front turn signal bulbs can crack and fail to illuminate, increasing the risk of crashes.
Product
NISSAN — NISSAN VERSA, TITAN, TITAN XD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1862-2021·2021-06-23
Better-Bladder ECMO Device May Collapse, Reducing Blood Flow
The Better-Bladder ECMO device used in cardiopulmonary bypass circuits may collapse during use, increasing venous line resistance and reducing blood flow. The recall affects 147 units distributed nationwide.
Product
The Better-Bladder (BB), part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass circuits. Model: BB14
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1864-2021·2021-06-23
GE Healthcare X-Ray Systems Affected by Display Image Distortion Defect
GE Healthcare interventional x-ray imaging systems can develop a display defect that splits and distorts live monitor images into two unequal parts. The defect affects 139 devices with worldwide distribution.
Product
GE Healthcare Innova IGS 3 (GTIN 00840682147378), Innova IGS 5 (GTIN 00840682124621), Innova IGS 6 (GTIN 00840682124614), Discovery IGS 7 (GTIN 00840682124638), and Discovery IGS 7 OR (GTIN00840682125888) interventional fluoroscopic x-ray systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1898-2021·2021-06-23
VENOVO Venous Stent System 8F deployment failure during insertion
The VENOVO Venous Stent System 8F may fail to expand properly upon deployment and remain connected to the delivery system, affecting approximately 12,258 devices worldwide including 7,234 in the United States.
Product
VENOVO Venous Stent System 8F Product Description(REF)/dimension: VENEL10040 /Venovo 8F 10/40/1200mm OUS; VENEL10060 /Venovo 8F 10/60/1200mm OUS; VENEL10080 /Venovo 8F 10/80/1200mm OUS; VENEL10100 /Venovo 8F 10/100/1200mm OUS; VENEL10120 /Venovo 8F 10/120/1200mm OUS…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1853-2021·2021-06-23
WorkMate Claris Cardiac Monitoring System Software Error Causes Loss of Functionality
Abbott's WorkMate Claris cardiac monitoring system may lose functionality or display a black screen during operation due to a software error affecting 4 distributed units.
Product
v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System, Model H700123. The WorkMate Claris" System is a computer-based electrocardiographic recording and monitoring system designed for efficient capture, display, and retrieval of surface and intracardiac signals…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1885-2021·2021-06-23
Medtronic perfusion tubing packs recalled for manufacturing weld defects
Medtronic recalls 11 packs of HY10Y54R4 Custom Perfusion System tubing manufactured with insufficient or incomplete welds. No injuries have been reported.
Product
Medtronic HY10Y54R4, Custom Pack HY10Y54R4 ECC PED 1/4, Custom Perfusion System, Sterile, Rx.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1868-2021·2021-06-23
Covidien Respiratory Filters Recalled for Sterilization Process Deviations
Covidien is recalling Adult-Pediatric Electrostatic Filter HMEs due to potential deviations in ethylene oxide sterilization parameters. Approximately 192,000 units were distributed worldwide.
Product
Adult-Pediatric Electrostatic Filter HME, Item Code 352/5877Z - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1893-2021·2021-06-23
Medtronic Custom Perfusion System Tubing Packs Recalled Due to Welding Defects
Medtronic is recalling 26 tubing packs from its Custom Perfusion System (Lot 221148857) due to potential manufacturing defects. Specific lots may have been manufactured with insufficient or incomplete welds.
Product
Medtronic BB7D76R13, Custom Pack BB7D76R13 CORR HL, Custom Perfusion System, Sterile, Rx.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1866-2021·2021-06-23
Electrostatic Filter Angled recalled for sterilization validation deviations
Covidien LP is recalling Electrostatic Filter Angled devices (Item 350S19006) due to potential deviations in ethylene oxide sterilization parameters. These respiratory airway devices for anesthetized patients may not meet required sterility standards.
Product
Electrostatic Filter Angled, Item Code 350S19006 - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1870-2021·2021-06-23
Atellica CH 930 Analyzer photometer lamp may produce inaccurate results
Siemens Healthcare Diagnostics is recalling Atellica CH 930 Analyzers with photometer lamps that may reach saturation without alerting users, potentially producing inaccurate patient test results.
Product
Atellica CH 930 Analyzer with Photometer Lamp (SMN 11075676) Siemens Material Number: 11067000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1880-2021·2021-06-23
Medtronic Perfusion System Tubing Packs Recalled for Defective Welds
Medtronic is recalling specific lots of Custom Pack HY8R62R13 E Pack perfusion system tubing due to manufacturing defects. Affected lots may have incomplete welds that could compromise device function during use.
Product
Medtronic HY8R62R13,Custom Pack HY8R62R13 E Pack, Custom Perfusion System, Sterile, Rx.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1897-2021·2021-06-23
VENOVO Venous Stent System Recalled for Deployment Malfunction
The FDA is recalling VENOVO Venous Stent System units due to reports that the proximal end may fail to expand immediately upon deployment and remain connected to the delivery catheter.
Product
VENOVO Venous Stent System 10F Product Description(REF)/dimension: VENEL16040 Venovo 10F 16/40/1200mm OUS VENEL16060 Venovo 10F 16/60/1200mm OUS VENEL16080 Venovo 10F 16/80/1200mm OUS VENEL16100 Venovo 10F 16/100/1200mm OUS VENEL16120 Venovo 10F 16/120/1200mm OUS…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1892-2021·2021-06-23
Medtronic Cardiac Perfusion Tubing Packs Recalled for Incomplete Welds
Medtronic is recalling specific lots of BB8M63R5 adult cardiac perfusion tubing packs due to incomplete welds in the manufacturing process. These defects could compromise tubing integrity during cardiac surgery.
Product
Medtronic BB8M63R5, Custom Pack BB8M63R5 Adult ECC, Custom Perfusion system, Sterile, Rx.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1856-2021·2021-06-23
Radiometer ABL90 FLEX Analyzer Recalled Due to Internal Clock Malfunction
Radiometer Medical ApS is recalling ABL90 FLEX Analyzers with E3800 PC units due to an internal clock issue. Approximately 3,346 units are affected globally, with only 2 in the United States.
Product
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1869-2021·2021-06-23
HME for Tracheostomized Patients Recalled Due to Sterilization Process Deviations
Covidien LP is recalling HME (Heat and Moisture Exchanger) units for tracheostomized patients due to potential deviations from validated ethylene oxide sterilization parameters. The recall affects 10,890 units distributed worldwide and in specific U.S. states.
Product
HME for Tracheostomized Patients, Item Code 353S13046 - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1848-2021·2021-06-23
Surgical Angio Pack Kits Recalled Due to Incomplete Angio Tubing Weld
Windstone Medical Packaging is recalling Angio Pack surgical kits (Lot 146304 and 147534) due to angio tubing with insufficient or incomplete welds.
Product
Angio Pack REF: AMS6908C, Sterile EO, Contents:1 Blade Scalpel # 11 SS 1 Bowl Guidewire 80 oz 4 Clamp Towel 2.5 1 Cover Probe 6X48 NS 2 Gown Surgical STD XLG NR 16 Label Custom 1 Counter Needle Nest 40 Sponge 4x4x12 plain 1 Syringe 10cc control polyc 1 Bag Band Dome 22…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1890-2021·2021-06-23
Medtronic Perfusion System Tubing Packs Recalled for Incomplete Welds
Medtronic is recalling HY10L28R3 perfusion system tubing packs (lot 221679870) manufactured with insufficient or incomplete welds. The recall affects units distributed in nine U.S. states.
Product
Medtronic HY10L28R3, Custom Pack HY10L28R3 1/4 Pack, Custom Perfusion System, Sterile, Rx.
Category
Medical Device
Distribution
Distributed nationwide