The Recall Desk

State

Alaska product recalls

73,584 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.

These figures cover only the 1,766 recalls whose distribution notice names Alaska specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27276–27300 of 75350

  • SevereFDA (Food)·F-0145-2021·2020-12-09

    Tanimura & Antle Romaine Lettuce Recalled Due to E. coli O157:H7 Detection

    Tanimura & Antle is recalling specific lots of Romaine lettuce after Michigan state officials detected E. coli O157:H7 during routine sampling.

    Product
    Tanimura & Antle brand Romaine lettuce. 1 head 12,15,018 and 24 case Product of USA UPC: 2-27918 20314-9 Tanimura & Antle, Salinas, CA
    Category
    Food
    Distribution
    19 states
  • SevereFDA (Devices)·Z-0516-2021·2020-12-09

    Medtronic MiniMed 670G Insulin Pumps Recalled for Battery Connection Defect

    Medtronic is recalling 391 MiniMed 670G insulin pumps because a missing solder battery connection could interrupt power to the device.

    Product
    MiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous or periodic monitoring of glucose levels in the fluid under the skin, and detecting possible low and high glucose episodes. When using a sensor and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·21046·2020-12-09

    L G Sourcing Recalls Electric Fireplaces Due to Fire Hazard

    L G Sourcing is recalling allen + roth 62-inch electric fireplaces sold at Lowe's because wiring connectors can overheat, posing a fire hazard.

    Product
    allen + roth 62-inch Electric Fireplaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0505-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model number: GF-UC160P-OL5 - Product Usage: used for diagnostic ultrasound imaging or fluid flow analysis of the human body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0501-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model number :GF-UM20 - Product Usage: used with other supporting equipment for endoscopic real-time ultrasound imaging and endoscopic surgery within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0531-2021·2020-12-09

    Verathon BladderScan Prime Plus Probe Recall for Handle Cracking Risk

    Verathon is recalling 398 BladderScan Prime Plus Probes because a change in handle material and process may cause the handle to crack.

    Product
    BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the bladder noninvasively.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0525-2021·2020-12-09

    CME America T-Syringe Pump Recalled for Motor Wear and Hardware Damage

    CME America is recalling T-Syringe Pumps because motor wear may cause silent under-infusion and cleaning fluids may crack hardware.

    Product
    CME America T-Syringe Pump -T34L - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0510-2021·2020-12-09

    VEO Diagnostics Recalls ACCEL ELISA COVID-19 Antibody Test Kits

    VEO Diagnostics is recalling 15 ACCEL ELISA COVID-19 antibody test kits because the FDA removed their Emergency Use Authorization. Users should stop using the kits.

    Product
    ACCEL ELISA COVID-19 for the detection of total antibodies to SARS-CoV-2 Catalog AE301U Kit lots: PXCOV073020, PXCOV081220 Expiration dates: January 18, 2021 and January 26, 2021
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0147-2021·2020-12-09

    Tucson Tamale Blue Corn and Veggie Tamales Recalled for Plastic Contamination

    Tucson Tamale Wholesale Company is recalling Blue Corn & Veggie Tamales because plastic pieces were found in the tomato cans used to make them.

    Product
    Tucson Tamale Blue Corn & Veggie Tamales (2 Pack), 11 OZ (312g), plastic bag, UPC 8 53437 00234, Keep Frozen, 6 packs/box (case)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0502-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model number: GF-UM130 - Product Usage: used with an Olympus Endoscopic Ultrasound Center, EVIS Video System Center, light source, documentation equipment, video monitor, Endo-Therapy accessories and other ancillary equipment for endoscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0517-2021·2020-12-09

    Medtronic MiniMed 630G Insulin Pump Recalled for Battery Connection Defect

    Medtronic is recalling 206 MiniMed 630G insulin pumps due to a missing solder battery connection that could interrupt power.

    Product
    MiniMed 630G with SmartGuard, insulin pump, Ref/Model # MMT-1754K, MMT-1714K, MMT-1755K - Product Usage: intended for continuous delivery of basal insulin (at user selectable rates) and administration of insulin boluses (in user selectable amounts) for the management of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0529-2021·2020-12-09

    CME America T-Syringe Pump Recalled for Motor Wear and Fluid Damage

    CME America is recalling 4,182 T-Syringe Pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may crack hardware.

    Product
    CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0148-2021·2020-12-09

    Tucson Tamale Blue Corn Veggie & Cheese Tamales Recalled for Plastic Contamination

    Tucson Tamale Wholesale Company is recalling specific lots of Blue Corn, Veggie & Cheese Tamales because plastic pieces were found in the tomato cans used to make them.

    Product
    Tucson Tamale Blue Corn, Veggie & Cheese Tamales (2 Pack), 11 OZ (312g), plastic bag, UPC 8 53437 00233, Keep Frozen, 6 packs/box (case)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21044·2020-12-09

    Fiskars Recalls 16-Foot Pole Saws Due to Laceration Hazard

    Fiskars is recalling 16-foot extendable pole saws and pruners because the telescoping poles can separate and fall, posing a laceration hazard.

    Product
    Fiskars 16 foot Extendable Pole Saw/Pruners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0513-2021·2020-12-09

    Biomeme SARS-CoV-2 PCR Test Recalled for False Positive Results

    Biomeme is recalling 105 units of its SARS-CoV-2 Real-Time RT-PCR Test because the software made false positive calls due to assay issues.

    Product
    The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in vitro diagnostic test that is based on widely used nucleic acid amplification technology. The Biomeme SARS-CoV-2 Real-Time RT-PCR Test contains primers and probes and internal controls used in RT-PCR for the in vitro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21047·2020-12-09

    CRAFTSMAN 10-Inch Corded Chain Saws Recalled for Laceration Hazard

    Black & Decker is recalling CRAFTSMAN 10-inch corded chain saws with extension poles because they may start unexpectedly, posing a laceration risk.

    Product
    CRAFTSMAN® CMECSP610 10-inch corded chain saws with extension poles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0506-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Infection Risk Mitigation

    Olympus is recalling ultrasound endoscopes to reduce the risk of patient infections by adding a new inspection step to the cleaning and disinfection instructions.

    Product
    Olympus Ultrasound Endoscope, Model number: GF-UCT160-OL5 - Product Usage: used for diagnostic ultrasound imaging or fluid flow analysis of the human body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21042·2020-12-09

    Neptune Benson Recalls Delta UV Generators for Pools Due to Fire Hazard

    Neptune Benson is recalling Delta UV EA-4H-10 generators for pools and spas because water leaks can cause overheating and fire. No injuries have been reported.

    Product
    Delta UV EA-4H-10 ultra-violet generators installed in swimming pools and swim spas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0507-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Infection Risk Reduction

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model number: GF-UE160-AL5 - Product Usage: used for endoscopic ultrasonic imaging of the gastrointestinal wall, bile and pancreatic ducts and surrounding organs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21050·2020-12-09

    Goal Zero Recalls Yeti 25A Fast Charge Power Supplies Due to Fire Hazard

    Goal Zero is recalling approximately 4,500 Yeti 25A Fast Charge power supplies because loose connections can overheat and cause a fire. No injuries have been reported.

    Product
    Yeti 25A Fast Charge Power Supplies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0520-2021·2020-12-09

    K2M Recalls Yukon Anti-Torque Alignment Tubes Due to Manufacturing Defect

    K2M, Inc. is recalling four Yukon Anti-Torque Alignment Tubes from Lot KTGG because shafts do not pass through the inner cannula, potentially delaying surgery.

    Product
    Yukon OCT Spinal System Yukon Anti-Torque Alignment Tube - Product Usage: The Anti-Torque Alignment Tube (the Alignment Tube ) provides counter rotation to reduce the torque applied to the anatomy when the size 15 Torque limiting shaft (the shaft is used to tighten the Yukon…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0499-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model Number: GF-UCT140-AL5 - Product Usage: used with other supporting equipment for endoscopic real-time ultrasound imaging and endoscopic surgery within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0503-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model number: GF-UMQ130 - Product Usage: used with an Olympus Endoscopic Ultrasound Center, EVIS Video System Center, light source, documentation equipment, video monitor, Endo-Therapy accessories and other ancillary equipment for endoscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0500-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model number: GF-UCT180 - Product Usage: used with an Olympus universal endoscopic ultrasound center or a diagnostic system (ALOKA CO. LTD), video system center, light source, documentation equipment, monitor, EndoTherapy accessories and other…
    Category
    Medical Device
    Distribution
    Distributed nationwide