State

Alaska product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4351–4375 of 74704

HighFDA (Devices)·Z-0470-2026·2025-11-19
Small jaw sealers recalled over residual material that may dislodge
Medline is recalling 18,117 reprocessed LigaSure Small Jaw instruments because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Small Jaw Instrument (Purple/White), Compatible with FT10 Generator 18.8 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0483-2026·2025-11-19
Fifteen millimetre snares recalled over holes compromising package sterility
Olympus is recalling 18,174 Single Use Electrosurgical Snares SD-400U-15 because sterility may be compromised by small holes formed during packaging or transportation.
Product
Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Single Use Single Use Electrosurgical Snare Model/Catalog Number: SD-U400U-15 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0453-2026·2025-11-19
Patient monitors recalled over batteries that can lose backup power
GE Healthcare is recalling 3,271 Carescape B450 patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.
Product
Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Record updated 3/19/26 to include: CARESCAPE B450 MBA313 2095800-001 CARESCAPE M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0472-2026·2025-11-19
Short blunt tip sealers recalled over residual material that may dislodge
Medline is recalling 65 reprocessed LigaSure Blunt Tip sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline RenewalLigasure Blunt Tip Sealer/Divider, NanoCoated Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2026·2025-11-19
Maryland jaw sealers 23 cm recalled over residual material inside the device
Medline is recalling 4,007 reprocessed LigaSure Maryland Jaw sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0499-2026·2025-11-19
Ceiling X-ray tube supports recalled over a shaft that may break
Shimadzu is recalling 1,766 ceiling type X-ray tube supports, models CH-200 and CH-200M, because the mounting shaft may break and the tube assembly could come off.
Product
Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The ceiling type x-ray tube support CH-200 is used to hold the X-ray tube and collimator to position the X-ray tube unit. This unit is used for radiographic ex
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0457-2026·2025-11-19
Monitor batteries recalled because they can lose the ability to charge
GE Healthcare is recalling 2,857 FLEX-3S2P lithium-ion batteries used with patient monitors because they can lose the capability to hold charge and provide backup power.
Product
BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, revision S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0455-2026·2025-11-19
Bedside patient monitors recalled over batteries that fail as backup power
GE Healthcare is recalling 7,408 B105P, B125P, B105M, B125M and B155M patient monitors because certain batteries can lose the ability to hold charge, causing a loss of monitoring.
Product
B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102 6160000-103 6160000-104 6160000-105 6160001-063 6160001-064 6160001-065 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms 3
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0183-2026·2025-11-19
Tense-X supplement recalled because it contains magnesium salicylate
Professional Botanicals is recalling 253 bottles of Tense-X capsules because the product contains magnesium salicylate.
Product
Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsules. Product Sku: PB207
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0477-2026·2025-11-19
Maryland jaw sealers 44 cm recalled over trapped residual material
Medline is recalling 9,547 reprocessed LigaSure Maryland Jaw sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0498-2026·2025-11-19
Long nasal feeding tubes recalled from one lot for possible occlusion
Applied Medical Technology is recalling NutraGlide 6 F-8 F x 90 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0469-2026·2025-11-19
Impact vessel sealers recalled over residual material that may dislodge
Medline is recalling 58,499 reprocessed LigaSure Impact sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.
Product
Medline Renewal Ligasure Impact Sealer/Divider NanoCoated, Compatible with FT10 Generator 18cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0486-2026·2025-11-19
VATS lobectomy stapler boxes recalled over a malformed cover tube press
Covidien is recalling two units of a VATS lobectomy box containing the Signia Small Diameter Curved Tip Intelligent Reload because internal components may move during firing.
Product
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0478-2026·2025-11-19
Spinal fixation screws recalled for not meeting performance standards
Orthofix is recalling 624 Virata preassembled polyaxial screws used in the Virata Spinal Fixation System because the screws do not meet performance standards.
Product
Virata Preassembled Polyaxial Screw, utilized in the Virata Spinal Fixation System. The following sizes are affected: 1. POLYAXIAL SCREW, CC, 5.5mm X 30mm; Item Number: TL1-10755030. 2. POLYAXIAL SCREW, CC, 5.5mm X 35mm; Item Number: TL1-10755035. 3. POLYAXIAL SCREW, CC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0456-2026·2025-11-19
Portrait vital signs monitors recalled over batteries losing backup power
GE Healthcare is recalling 5,990 Portrait VSM patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.
Product
Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0490-2026·2025-11-19
Reprocessed ultrasonic shears recalled because they may stick in the on position
Stryker Sustainability Solutions is recalling 22,476 reprocessed HARMONIC FOCUS shears because a manufacturing issue may leave them stuck in the on position, causing continuous activation.
Product
HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use, STERILEEO, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0491-2026·2025-11-19
Oak mix allergen tests recalled over barcode orientation misreading tube positions
Siemens Healthcare Diagnostics is recalling 34 units of IMMULITE 2000 Oak Mix Specific Allergen because barcode orientation causes the instrument to misread tube positions in the holder wedge.
Product
IMMULITE 2000 Oak Mix Specific Allergen; Siemens Material Number (SMN): 10386105; Catalog Number: L2KUN6;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0489-2026·2025-11-19
Hematology analyzers recalled because saturation flags may not be applied
Abbott Laboratories is recalling 833 Alinity hq Analyzers because a software issue means the system does not visibly flag results when saturation is present, which may give incorrect results.
Product
Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Model/Catalog Number: 09P68-01 Software Version: 5.0 to 5.10.1 for OUS, 5.7 and 5.10.1 in the US Product Description: Alinity hq Analyzer Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0496-2026·2025-11-19
Ninety centimetre nasal feeding tubes recalled for possible occlusion
Applied Medical Technology is recalling NutraGlide 5 F-6 F x 90 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0495-2026·2025-11-19
Nasal feeding tubes recalled from one lot because they may be occluded
Applied Medical Technology is recalling NutraGlide 5 F-6 F x 55 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0492-2026·2025-11-19
Allergy IgE universal kits recalled over barcodes misordering tubes in wedges
Siemens Healthcare Diagnostics is recalling 2,802 units of the 3gAllergy Specific IgE Universal Kit because barcode orientation causes the instrument to misread tube positions.
Product
3gAllergy Specific IgE Universal Kit; Kit Component: 3gAllergy Specific IgE Adjustor Antibody (L2UNS1), 3gAllergy Specific IgE Control Antibody (L2UNS2); Siemens Material Number (SMN): 10380875; Catalog Number: L2KUN6;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V800000·2025-11-19
McNeilus Recalls 2024-2025 Volterra ZSL Trucks Due to Software Error
McNeilus is recalling 2024-2025 Volterra ZSL side loader garbage trucks because a software error may cause grabber fingers to move without operator input, posing a risk of injury or crash.
Product
MCNEILUS — MCNEILUS VOLTERRA ZSL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0493-2026·2025-11-19
Food allergen panels recalled over barcodes causing wrong tube scanning order
Siemens Healthcare Diagnostics is recalling 28 units of Food Panel 3 Specific Allergen because barcode orientation causes the instrument to misread tube positions in the holder wedge.
Product
Food Panel 3 Specific Allergen; Siemens Material Number (SMN): 10385891; Catalog Number: FP3L4;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0497-2026·2025-11-19
Larger bore nasal feeding tubes recalled for possible occlusion
Applied Medical Technology is recalling NutraGlide 6 F-8 F x 55 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06055-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0468-2026·2025-11-19
Curved large jaw sealers recalled over residual material that may dislodge
Medline is recalling one reprocessed LigaSure Impact Curved Large Jaw sealer/divider because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Impact Curved Large Jaw Sealer/Divider, Compatible with FT10 Generator, FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide