The Recall Desk

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.

21501–21525 of 75153

  • HighFDA (Devices)·Z-0903-2022·2022-04-20

    Access-9 Hemostasis Valves Recalled for Guidewire Entrapment Risk

    Merit Medical Systems is recalling 36,445 Access-9 Large Bore Hemostasis Valves due to an internal gap that can trap the guidewire, potentially delaying medical procedures.

    Product
    Access-9 Large Bore Hemostasis Valves, Catalog Code: 580775001, IN8112/C, K05-00053H, K05-00109G, K05-00137K, K05-00410G, K05-00438G, K05-00502F, K05-00587D, K05-01052, K05-01706C, K05-01880K, K05-02130, K05-02595, K09-12599A, K10-05487P, K12-00264, MAP111/F, MAP112/B, MAP112/F…
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Food)·F-0983-2022·2022-04-20

    Kroger Buttermilk Pancake & Waffle Mix Recalled for Foreign Material Contamination

    Kroger Buttermilk Pancake & Waffle Mix with specific lot codes may contain foreign materials. Consumers who purchased this product should not use it.

    Product
    Item # 714-0706, Kroger Buttermilk Pancake & Waffle Mix. Product is shelf stable and packaged in a box. net wt. 2 lbs., UPC 0 11110 88219 6.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0934-2022·2022-04-20

    Surgical Head Fixation Device Mount Clamp Assembly Deflection Recall

    Deerfield Imaging recalls the Trumpf Mount Clamp Assembly component used in surgical head fixation devices. The clamp may deflect during use and become difficult to loosen after procedures, potentially requiring surgical intervention.

    Product
    Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a component of the IMRIS HFD100 head fixation device, models #119629-000 and #119630-000, which are used with ORT400 operating room tables.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0910-2022·2022-04-20

    Orthopedic Surgical Instrument Kit Recalled for Improper Driver Fit

    The Nextra Hammertoe Correction System surgical kit is being recalled due to an oversized driver that cannot properly connect to and remove from the implant. This defect can delay surgery.

    Product
    Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: NX-4532K Orthopedic surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0985-2022·2022-04-20

    Krusteaz Buttermilk Pancake Mix Product Recalled Nationwide for Foreign Materials

    Krusteaz Buttermilk Pancake Mix (Lot code KX2066, best-by 3/6/2024) is being recalled nationwide due to foreign materials. Consumers should not consume this product.

    Product
    Item # 721-0200, Krusteaz Buttermilk Pancake Mix. Product is shelf stable and packaged in a box. net wt. 2 lbs., UPC 0 41449 00110 4.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0990-2022·2022-04-20

    Gordon Choice Yellow Cake Mix nationwide recall for foreign materials

    Continental Mills is recalling Gordon Choice Yellow Cake Mix (lot KX2066) nationwide due to the presence of foreign materials. The recall was voluntarily initiated on March 10, 2022.

    Product
    Item # 744-4875, Gordon Choice Yellow Cake Mix. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 93901 24575 5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0935-2022·2022-04-20

    ECG Electrode Set Fails Electrical Safety, May Prevent Effective Defibrillation

    Graphic Controls' CLARAVUE pediatric electrode set fails electrical safety standards. The device may not deliver adequate charge during defibrillation, potentially rendering emergency treatment ineffective.

    Product
    CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776 50401-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0943-2022·2022-04-20

    Ventilator trolley mounting brackets can detach and cause device to fall

    The mounting brackets on Breas Ventilator Trolleys can become detached, allowing ventilators to fall. This poses an injury risk to people near the equipment.

    Product
    Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS ventilator models Article no 007384
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0921-2022·2022-04-20

    Abbott Vascular 20/30 Indeflator Recalled for Leaks and Connection Failures

    Abbott Vascular recalls 20/30 Indeflator medical devices due to increased complaints of leaks and loose connections. The recall affects 17 product lots distributed nationwide and internationally.

    Product
    20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0941-2022·2022-04-20

    Medline Laryngeal Masks recalled due to potential cuff disconnection

    Medline Industries is recalling approximately 8,990 cases of Standard PVC Laryngeal Masks distributed nationwide because the mask cuff may disconnect from the breathing tube.

    Product
    Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V267000·2022-04-20

    Certain BMW Vehicles: Sunroof May Close Without Key Fob Present

    BMW is recalling 2019-2023 X5, X6, X7, and 4 Series vehicles because the sunroof may close without the key fob inside, creating injury risk. Dealers will reprogram the control unit free of charge.

    Product
    BMW — BMW X7, X5, X6, M440I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0936-2022·2022-04-20

    Recalled CLARAVUE Pre-wired Electrode Set May Fail During Defibrillation

    Graphic Controls is recalling CLARAVUE Pre-wired Electrode sets because they fail to meet electrical safety specifications for defibrillators, potentially delivering inadequate charge during emergency treatment.

    Product
    CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600 US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0991-2022·2022-04-20

    Fish Breader Recalled Nationwide for Foreign Material Contamination

    Continental Mills is recalling Gordon Choice Southern Style Fish Breader (Lot KX2065) nationwide due to the presence of foreign materials. Consumers should not consume this product and should return it to the place of purchase.

    Product
    Item # 744-4930, Gordon Choice Southern Style Fish Breader. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 93901 75622 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0912-2022·2022-04-20

    Orthopedic surgical hammertoe instrument recalled for improper component sizing

    Nextremity Solutions is recalling the Nextra Hammertoe Correction System due to an oversized driver component that makes it difficult to properly connect and remove during surgery.

    Product
    Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: NX-3532K Orthopedic surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0987-2022·2022-04-20

    IHOP Pancake Mix Recalled Nationwide for Foreign Material Contamination

    Continental Mills is recalling 240 cases of IHOP Pancake Mix (Item #743-0278) nationwide due to the presence of foreign materials. Affected lots are KX2062 and KX2063 with a best-by date of 9/1/2022.

    Product
    Item # 743-0278, IHOP Pancake. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 41449 47540 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0939-2022·2022-04-20

    Cardiac electrode fails electrical safety test; defibrillation may not work

    The CLARAVUE Pre-wired Electrode does not meet electrical safety standards for defibrillators. It may not deliver effective electrical charge during emergency defibrillation.

    Product
    CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780 50603-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0914-2022·2022-04-20

    Orthopedic surgical driver oversized, affecting hammertoe correction

    Nextremity Solutions is recalling the Nextra Hammertoe Correction System Driver (SKU: NX-DR) due to oversizing at the proximal end, which impairs connection and removal from the implant, causing surgical delays. The defect affects 239 units distributed in the US, Japan, and the Netherlands.

    Product
    Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0904-2022·2022-04-20

    AccessPLUS hemostasis valves recalled for internal guidewire entrapment risk

    Merit Medical is recalling AccessPLUS Large Bore Hemostasis Valves due to an internal design gap that can trap guidewires, potentially delaying medical procedures.

    Product
    AccessPLUS Large Bore Hemostasis Valves, Catalog Code: 580758001, 580774001, IN8152/C, K04-01197, K05T-01863, K09-09102B, K09-10388A, K09-12917, K09-13501AP, K10-05457AP, K10-05635, K10-05868P, K10-05872P, K12-08303, K12-10346, K12-10375, K12-10724AP, K12-10962, K12-11413…
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Devices)·Z-0923-2022·2022-04-20

    Abbott Vascular Cardiovascular Device Recalled for Leaks and Loose Connections

    Abbott Vascular is recalling the 20/30 Priority Pack w/COPILOT device due to an increase in complaints of leaks and loose connections. The recall affects 131 lots distributed nationwide and internationally.

    Product
    20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0986-2022·2022-04-20

    Krusteaz Pro Buttermilk Pancake Mix Recalled Nationwide for Foreign Materials

    Krusteaz Pro Buttermilk Pancake Mix is being recalled due to potential foreign materials. Approximately 970 cases with specific lot codes were distributed nationwide.

    Product
    Item # 731-0120, Krusteaz Pro Buttermilk Pancake Mix. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 41449 10180 4.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0906-2022·2022-04-20

    Integra Universal Flexible Arm Recall: Internal Cable May Break

    Integra LifeSciences is recalling the Universal Flexible Arm (part number REF 1362275) because excess tightening force can break the internal cable at the tip, rendering the device unusable.

    Product
    Integra Universal Flexible Arm part number REF 1362275
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0992-2022·2022-04-20

    Tattooed Chef Plant-Based Sausage Breakfast Bowl Recalled for False Gluten-Free Claim

    Ittella International recalls Tattooed Chef Plant-Based Sausage Breakfast Bowls nationwide due to an incorrect gluten-free claim on the container lid. The product contains wheat flour, which is correctly listed in the ingredients and allergen statement.

    Product
    Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life Box Net wt. 40oz (1.13kg) UPC: 850015982569 Packed for: Tattooed Chef Paramount, CA 90723
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0769-2022·2022-04-20

    Lansoprazole Delayed-Release Capsules Recalled for Out-of-Specification Dissolution

    Preferred Pharmaceuticals is recalling certain lots of Lansoprazole Delayed-Release Capsules 15mg due to dissolution testing results that do not meet specifications. Approximately 791 bottles were distributed nationwide.

    Product
    Preferred Pharmaceuticals, Inc. The Physician's Solution., Lansoprazole Delayed-Release Capsules, 15mg, Generic for Prevacid, 90-Count Bottle, Manufacturer: Dr Reddy's Laboratories Limited, NDC 68788-6390-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0924-2022·2022-04-20

    Abbott INDEFLATOR Plus 30 Device Recalled for Leaks and Connection Faults

    Abbott Vascular is recalling INDEFLATOR Plus 30 balloon inflators due to increasing complaints of leaks and intermittent loose connections that could affect device function during medical procedures.

    Product
    INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)
    Category
    Medical Device
    Distribution
    Distributed nationwide