State

Alaska product recalls

73,388 recalls have nationwide distribution and so reach Alaska. 1,765 additional recalls listed Alaska specifically in their distribution scope.

What the numbers show

Total: 1,765
Critical: 118
Severe: 470
Most recent: 2026-09-23

Of the 1,765 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 1,765 recalls whose distribution notice names Alaska specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20251–20275 of 75153

HighFDA (Devices)·Z-1368-2022·2022-07-20
Dental bonding primer may lack resin component affecting restoration
Ultradent Peak Universal Bond self-etch dental primers may be missing resin, potentially compromising bond strength. Affected products were distributed nationwide and internationally.
Product
Peak Universal Bond Self-Etch Bottle Kit, Part: 4541; Peak Universal Bond Self-Etch Intro Kit, Part: 4554; Peak SE Primer 4pk Refill, Part: 5135; Peak Universal Bond Sample SE, Part: S4554. For use in light-curing dental bonding procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1210-2022·2022-07-20
Compounded injectable product recalled for lack of sterility assurance
Tailor Made Compounding is recalling 25 vials of a compounded injectable product due to lack of assurance of sterility. The affected batches were distributed nationwide.
Product
Inositol/Choline B12 + Carnitine 40mg/40mg/1mg/100mg/mL, 30mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1206-2022·2022-07-20
Tailor Made Compounding Recalls Glycyrrhizic Acid Injectable for Lack of Sterility Assurance
Tailor Made Compounding recalls 101 vials of Glycyrrhizic Acid (8mg/mL) nationwide due to lack of assurance of sterility in this injectable preparation. Patients should contact their healthcare provider.
Product
Glycyrrhizic Acid 8mg/mL, 10mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1218-2022·2022-07-20
Methylene Blue Hypotonic Solution Vials Recalled for Sterility Assurance Failure
Methylene Blue Hypotonic Solution vials are being recalled nationwide and in Puerto Rico due to lack of assurance of sterility. Affected vials should not be used.
Product
Methylene Blue Hypotonic Solution, 10mg/mL, a) 2 mL-vial, b) 10mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1326-2022·2022-07-20
Radiography System Firmware Error May Cause Incorrect Radiation Dose
Philips DigitalDiagnost 4 radiography systems may deliver incorrect radiation doses due to a Wallstand VS2 firmware issue causing incorrect image orientation and misaligned anatomical markers.
Product
DigitalDiagnost 4 High Performance. radiography and fluoroscopy system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1222-2022·2022-07-20
Procaine HCL Injectable Recalled Due to Sterility Assurance Concerns
Tailor Made Compounding is recalling Procaine HCL 2% injectable solution due to lack of sterility assurance. The recall affects 58 vials distributed nationwide.
Product
Procaine HCL 2% (20mg/mL), 30 ml-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1325-2022·2022-07-20
Philips ProxiDiagnost N90 radiography system: firmware issue causes incorrect radiation dose
Philips is recalling 140 ProxiDiagnost N90 radiography systems due to a firmware issue in the Wallstand VS2 component. After system restart or first exposure with Wallstand VS2, the system may deliver incorrect radiation doses and misposition anatomic markers.
Product
ProxiDiagnost N90. radiography and fluoroscopy system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1355-2022·2022-07-20
MiniMed 670G Insulin Pump Battery Cap Defect Causing Power Loss
MiniMed 670G Insulin Pump may lose power due to battery cap deterioration, affecting approximately 279,251 units distributed in the U.S. and overseas.
Product
MiniMed 670G Insulin Pump (U.S. and O.U.S. Version)
Category
Medical Device
Distribution
53 states
HighFDA (Drugs)·D-1243-2022·2022-07-20
Glutathione Injectable Vials Recalled Due to Sterility Assurance Concerns
Tailor Made Compounding is recalling Glutathione 200mg/ml injectable vials due to lack of assurance of sterility. The recall affects 485 vials distributed nationwide in the USA and Puerto Rico.
Product
Glutathione 200mg/ml, a) 10ml-vial, b) 30ml-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1203-2022·2022-07-20
FDA Recalls Tailor Made Compounding GAC Injectable Vials for Lack of Sterility Assurance
Tailor Made Compounding is recalling 90 vials of GAC (Glutamine/Arginine/L-Carnitine) injectable solution distributed nationwide and in Puerto Rico due to lack of assurance of sterility.
Product
GAC (Glutamine/Arginine/L-Carnitine) 25mg/100mg/250mg/mL, 30mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1223-2022·2022-07-20
PT-141 10mg/mL Injectable Vials Recalled for Sterility Assurance Concerns
Tailor Made Compounding is recalling PT-141 10mg/mL vials nationwide due to inability to assure sterility. The recall affects 392 vials in 1mL and 2mL sizes distributed in 2022.
Product
PT-141 10mg/mL a) 1mL-vial, b) 2 mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1224-2022·2022-07-20
Semaglutide/Cyanocobalamin Injectable Recalled for Lack of Sterility Assurance
Tailor Made Compounding is recalling 5,842 vials of compounded semaglutide/cyanocobalamin injectable due to lack of sterility assurance. The product was distributed nationwide in the United States and Puerto Rico.
Product
Semaglutide/Cyanocobalamin 2mg/0.4mg/ml, 1mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1236-2022·2022-07-20
Compounded Testosterone Injection Recalled Due to Lack of Sterility Assurance
Tailor Made Compounding is recalling 176 vials of testosterone cypionate/propionate injectable due to lack of assurance of sterility. The product was distributed nationwide.
Product
Testosterone Cypionate/Propionate 180/20mg/ml, a) 5 mL-vial, b) 10 mL-vial, Room temperature, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1235-2022·2022-07-20
Testosterone Injections Recalled for Lack of Sterility Assurance
Tailor Made Compounding is recalling 246 vials of compounded testosterone injections distributed nationwide due to lack of assurance of sterility. Non-sterile injectable medications may pose a risk of infection.
Product
Testosterone Cypionate/Enanthate/Propionate 80/80/40mg, a) 5 mL-vial, b) 10 ml-vial, Room temperature, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V514000·2022-07-20
Volkswagen Atlas Cross Sport Rearview Camera Software Defect Recall
Volkswagen is recalling certain 2021-2022 Atlas Cross Sport vehicles due to an infotainment system defect that may prevent the rearview camera image from displaying. This loss of rear visibility increases crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN TAOS, ATLAS, TIGUAN, JETTA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V515000·2022-07-20
Audi Recalls 2022 A3 and S3 Sedans for Seat Belt Tensioner Defect
Volkswagen Group of America is recalling 2,584 2022 Audi A3 and S3 sedans because the seat belt tensioners may not restrain occupants properly during a crash.
Product
AUDI — AUDI A3, S3
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1213-2022·2022-07-20
Compounded Injectable Medication Recalled Due to Sterility Assurance Concerns
Tailor Made Compounding is recalling 924 vials of Methionine/Inositol/Choline B12 + Carnitine injectable compound nationwide due to lack of assurance of sterility.
Product
Methionine/Inositol/Choline B12 + Carnitine 10mg/40mg/40mg/1mg/100mg/mL, a) 4mL-vial, b) 10 mL-vial, c) 30mL- vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1227-2022·2022-07-20
Compounded Sermorelin/Glycine Injectable Vials Recalled for Lack of Sterility Assurance
Tailor Made Compounding is recalling 1,562 vials of Sermorelin/Glycine injectable distributed nationwide because the manufacturer cannot assure the product meets sterility standards. Patients should stop using the recalled product and contact their healthcare provider.
Product
Sermorelin/Glycine 2000mcg/5mg/mL, 4mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1205-2022·2022-07-20
Glutathione Injectable Compounded Drug Recalled Due to Sterility Assurance Issues
Tailor Made Compounding recalls Glutathione 200mg/mL injectable vials due to lack of sterility assurance. The FDA Class II recall affects 40 vials distributed nationwide.
Product
Glutathione 200mg/mL Preservative Free, Injectable, 30mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1211-2022·2022-07-20
Levocarnitine Injection Recalled Due to Lack of Sterility Assurance
Tailor Made Compounding is recalling Levocarnitine 500mg/mL vials nationwide due to lack of sterility assurance, a Class II FDA recall.
Product
Levocarnitine 500mg/mL, 30mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1190-2022·2022-07-20
Testosterone Cypionate Injection Recalled for Water Leakage in Manufacturing
Sun Pharmaceutical recalls 50,860 vials of Testosterone Cypionate Injection due to water leakage during manufacturing that could affect product sterility. The firm-initiated recall was reported in July 2022 and affects nationwide distribution.
Product
TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1346-2022·2022-07-20
CoolMax ZELTIQ Vacuum Applicator recalled for paradoxical hyperplasia complaints
Zeltiq Aesthetics is voluntarily discontinuing 2,945 CoolMax ZELTIQ Vacuum Applicators due to an increase in paradoxical hyperplasia complaints between 2019 and 2021, an adverse event causing unwanted tissue growth instead of intended fat reduction.
Product
CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000
Category
Medical Device
Distribution
52 states
HighFDA (Drugs)·D-1202-2022·2022-07-20
Folic Acid Injectable Vials Recalled Due to Sterility Concerns
TMC Acquisition LLC is recalling Folic Acid 5mg/mL injectable vials due to lack of assurance of sterility. The recall affects 45 units distributed nationwide and in Puerto Rico.
Product
Folic Acid 5mg/mL, 30mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1204-2022·2022-07-20
Compounded Injectable Amino Acid Drug Recalled for Sterility Assurance Issues
Tailor Made Compounding is recalling 60 GOAL injectable vials nationwide due to lack of sterility assurance, which may pose a contamination risk.
Product
GOAL (Glutamine/Ornithine/Arginine/Lysine 25mg/75mg/150mg/250mg/ml) 30 ml-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1192-2022·2022-07-20
Alpha Lipoic Acid injectable vials recalled for sterility assurance failure
TMC Acquisition LLC is recalling Alpha Lipoic Acid 25mg/mL vials due to lack of assurance of sterility in manufacturing. The product was distributed nationwide.
Product
Alpha Lipoic Acid 25mg/mL, 30mL-vial, Refrigerate, Tailor Made Compounding
Category
Drug
Distribution
Distributed nationwide