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.

3626–3650 of 74704

HighFDA (Drugs)·D-0286-2026·2026-01-21
Deodorant products recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Deodorant products over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Deodorant: a) Axe, Body Spray, Wild Spice, 6CT, 150ML, UPC: 600108736469; b) LUCKY MENS STICK DEODORANT, SPRING FRESH, 24CT, 2.5 OZ, UPC: 808829111668; c) LUCKY MENS STICK DEODORANT, FRESH COMFORT, 24CT, 1.6 OZ, UPC: 808829089103; d) LADY DEODORANT, CHERRY BLOSSOSM, 24CT, 1.8oz,
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0278-2026·2026-01-21
Halls cough drops recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Halls Cough Drops across multiple flavours over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Halls Cough Drops a) BAGS, MENTHOL, 12CT; b) BAGS, HONEY LEM, 12CT; c) BAGS, DEFENSE CITRUS, 12CT; d) BAGS, CHERRY, 12CT; e) M. CHERRY, 20 STK; f) BRAZIL, Cherry, 21CT/27.5G; f) LEMON. HONEY, 20CT #1180E; g) LIME FRESH, 20CT, #1182; h) MENTHOL BLUE, 20CT, #1180A; i) BRAZIL, Menth
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1093-2026·2026-01-21
Cell wash solution recalled over fungal contamination of an affected lot
Hologic is recalling 3,728 units of ThinPrep CytoLyt Solution over fungal contamination of the affected lot with Parengyodontium album.
Product
ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1101-2026·2026-01-21
Spinal tray syringes recalled over a crack on the syringe collar
ICU Medical is recalling 64,290 Portex Spinal Trays because syringes may have a crack on the collar, which may lead to delayed or repeated blood draws and blood leakage.
Product
Portex Spinal Tray, Item No. A3729-24 A3595
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0282-2026·2026-01-21
Carmex lip balm recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Carmex over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Carmex a) jar, 12 count, UPC: 083078123154, 083078113155; b) Tube, PEG, 12 count, UPC: 083078123147, 083078113148
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0277-2026·2026-01-21
Tylenol products recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Tylenol over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
TYLENOL a) 500 MG., 2'S DISPLAY, 50CT; b) COLD & FLU, 25CT/2S; c) COLD & FLU SEVERE, 2PK, 50CT; d) PM, 50CT; e) SINUS SEVERE, 2PK, 50CT
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1094-2026·2026-01-21
Infusion pumps recalled over speakers that may not produce audible alarms
ICU Medical is recalling 423 Plum Duo Infusion Systems after one lot of defective primary speakers may fail to produce sound, so the pump may not produce audible alarms or alerts.
Product
Plum Duo Infusion System, List Number 40002-04-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0272-2026·2026-01-21
Liquid NyQuil recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Liquid NyQuil over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
LIQUID NYQUIL a) regular, 12/8oz; b) cherry, 12/8oz
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1071-2026·2026-01-21
MRI systems recalled over ice that may block the magnet venting system
Canon Medical Systems is recalling 34 Vantage Galan 3T MRI systems because ice may form in the venting system, and a quench in that condition could rupture the helium vessel.
Product
Allura Xper FD20 Biplane; Model Number: 722013;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1092-2026·2026-01-21
Patient positioning systems recalled over stereotactic radiosurgery tolerance errors
C-RAD Positioning is recalling 189 Catalyst and Catalyst+ systems because the system may indicate a patient as correctly positioned at the isocenter when it is outside tolerance.
Product
Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version: cSRS module in combination with cMotion module Product Description: GMDN: 40893 Patient positioning device, diagnostic imaging/radiotherapy, laser Component
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1079-2026·2026-01-21
Azurion interventional systems recalled over nine identified software issues
Philips Medical Systems Nederland is recalling 990 Azurion R3.0 systems over nine identified software issues, including loss of X-ray after a pedal tap and continuous restart.
Product
Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. Azurion 3 M15. Model Number: 722230. 3. Azurion 5 M12. Model Number: 722231. 4. Azurion 5 M20. Model Number: 722232. 5.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0401-2026·2026-01-21
SMV BodyTrack nuclear medicine systems recalled over a potential detector fall
GE HealthCare is recalling 12 units of the SMV BodyTrack nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.
Product
Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. 32 OZ (2 LB) 907g UPC: 1 93968 00697 6
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0261-2026·2026-01-21
Frozen raw shrimp recalled over elevated levels of chloramphenicol
AZ Gems is recalling 1,099 cases of Member's Mark Jumbo Raw Shrimp over elevated levels of chloramphenicol.
Product
Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559
Category
Food
Distribution
Distributed nationwide
HighNHTSA·26V026000·2026-01-21
Keystone Recalls Travel Trailers Due to Ramp Door Breakage Risk
Keystone RV Company is recalling 2024-2026 Fuzion, Raptor, Redwood, and Voltage travel trailers because the ramp door may break away from the frame, increasing injury risk.
Product
KEYSTONE — KEYSTONE VOLTAGE, REDWOOD, RAPTOR, FUZION
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1018-2026·2026-01-21
MRI systems recalled over ice that may block magnet venting
Canon Medical Systems is recalling 22 Vantage Titan 3T MRI systems because ice in the magnet venting system could lead to a helium vessel rupture during a quench.
Product
VANTAGE TITAN 3T Model MRT-3010/MEXL-3010
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V029000·2026-01-21
Alexis Fire Equipment Recalls Two Tanker Trucks Due to Loose Fasteners
Alexis Fire Equipment is recalling two tanker trucks (2022 and 2024) because loose axle clamp fasteners may cause a loss of vehicle control.
Product
ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0273-2026·2026-01-21
NyQuil Cold and Flu recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling NyQuil Cold and Flu over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
NYQUIL COLD & FLU -32CT/2PK
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0263-2026·2026-01-21
Alka Seltzer recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Alka Seltzer over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1088-2026·2026-01-21
Robotic and gynaecology kits recalled over leaking suction irrigators inside
Medline is recalling 12,584 procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.
Product
Medline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M; 2) ROBOTIC GYN, REF CDS980647K; 3) DAVINCI PROCEDURE, REF CDS980864Q; 4) GYN-URO LAPSCP CDS-LF, REF CDS981583U; 5) GYN-URO LAPSCP CDS-LF, REF CDS981583V; 6) GYN ROBOTIC, REF CDS981826K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1064-2026·2026-01-21
Allura Xper FD10, model 722003, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 93 units of the Allura Xper FD10, model 722003, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10; Model Number: 722003;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1070-2026·2026-01-21
Surgical procedure packs recalled over recalled B. Braun administration sets inside
Medline is recalling 338 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Allura Xper FD20; Model Number: 722012;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1051-2026·2026-01-21
Pre-op kits recalled because they contain recalled B. Braun administration sets
Medline is recalling 32 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1054-2026·2026-01-21
Facial procedure packs recalled over recalled B. Braun administration sets inside
Medline is recalling 16 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: DR HOLCOMB FACIAL PACK, Medline kit SKU DYNJ54488A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1017-2026·2026-01-21
Allura Xper FD20 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 79 units of the Allura Xper FD20, model 722012, because the drip tray beneath the cooling unit may not have been installed.
Product
VANTAGE GALAN 3T Model MRT-3020/MEXL-3020
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1039-2026·2026-01-21
Spinal instrument sets recalled because the rotation tool handle can untread
Medicrea International is recalling 44 IB3D PL Instruments Sets because, following complaints, the orthopedic rotation tool handle may untread from the shaft.
Product
Medicrea, IB3D PL Instruments Set, Rx Only REF: SPS03174
Category
Medical Device
Distribution
Distributed nationwide