The Recall Desk

State

Alaska product recalls

73,491 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 73,491 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22876–22900 of 75257

  • ModerateFDA (Drugs)·D-0297-2022·2022-01-05

    Betamethasone Dipropionate Lotion recalled for failed stability test

    Teligent Pharma is recalling Betamethasone Dipropionate Lotion USP 0.05% (Augmented) due to failure to meet specification for the Active Pharmaceutical Ingredient particle test during routine stability testing.

    Product
    Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC 52565-023-29
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0436-2022·2022-01-05

    VIDAS Lyme IgM II Diagnostic Test Kits Recalled for Substrate Error

    bioMerieux is recalling three lots of VIDAS Lyme IgM II diagnostic test kits due to a substrate error that prevents the test from running, requiring users to conduct another test to obtain results.

    Product
    VIDAS Lyme IgM II (LYM), REF 416436
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0432-2022·2022-01-05

    VIDAS RUB IgG Diagnostic Test Kit Recalled for Substrate Defect

    bioMerieux is recalling three lots of VIDAS RUB IgG test kits due to substrate errors that prevent the test from running, potentially delaying diagnostic results.

    Product
    VIDAS RUB IgG (RBG), REF 30226
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0424-2022·2022-01-05

    FDA Recalls VIDAS PRG Progesterone Test Kits for Substrate Error

    bioMerieux is recalling 1,818 units of VIDAS PRG Progesterone test kits due to a substrate error that prevents the tests from running properly, causing delayed results when patients need repeat testing.

    Product
    VIDAS PRG Progesterone, REF 30409-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V002000·2022-01-04

    LGS Industries Recalls 2014-2021 Trailers with Electric Rear Door Winch Defect

    LGS Industries is recalling 2014-2021 trailers because the electric rear door winch cable may break, allowing the door to fall open and increasing injury risk.

    Product
    LGS INDUSTRIES — LGS INDUSTRIES PREMIER RACE, SHADOW, CARGO SPORT, JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V001000·2022-01-01

    Rosenbauer Fire Trucks Recalled for Fuel Tube Cracking and Fire Risk

    Rosenbauer America is recalling 2018-2022 fire trucks because fuel tubes may crack, causing high-pressure leaks that could lead to fire.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, WARRIOR, COMMERCIAL 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0288-2022·2021-12-29

    Moxifloxacin 1 mg/mL Solution Label Mix-up Recall

    Denver Solutions, LLC (doing business as Leiters Health) is recalling Moxifloxacin 1 mg/mL intracameral injection solution because vials labeled as 1 mg/mL may actually contain 5 mg/mL, creating a serious dosing error risk.

    Product
    Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796 Compark Blvd, Englewood, CO 80112, (800) 292-6772, NDC 71449-096-42
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0293-2022·2021-12-29

    OTC Cough and Cold Drug Recalled for Microbial Contamination

    Efficient Laboratories is recalling approximately 4,026 bottles of Rompe Pecho Max Multi-Symptoms cough and cold medicine nationwide due to potential microbial contamination of the non-sterile product.

    Product
    ROMPE PECHO MAX MULTI SYMPTOMS — ROMPE PECHO MAX MULTI SYMPTOMS (ACETAMINOPHEN, DEXTROMETHOPHAN HBR, PHENYLEPHRINE HCL, GUAIFENESIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0292-2022·2021-12-29

    OTC Expectorant Recall: Microbial Contamination in Rompe Pecho

    Efficient Laboratories is recalling Rompe Pecho guaifenesin expectorant in 4 fl oz and 6 fl oz bottles due to microbial contamination of non-sterile products. The affected product was distributed nationwide.

    Product
    ROMPE PECHO — ROMPE PECHO (GUAIFENESIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0383-2022·2021-12-29

    Stealthstation and Synergy Cranial surgical navigation system software synchronization error

    Stealthstation and Synergy Cranial surgical navigation systems may display an incorrect biopsy needle position due to software synchronization failure. This could result in prolonged surgery, additional procedures, or tissue injury.

    Product
    Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial, Model: 9733763, and StealthStation Cranial, Model: 9735585
    Category
    Medical Device
    Distribution
    51 states
  • SevereFDA (Devices)·Z-0394-2022·2021-12-29

    WIRION Embolic Protection System Filter Withdrawal Difficulties

    Cardiovascular Systems Inc recalls WIRION Embolic Protection System devices (6Fr) because the filter assembly may become difficult to withdraw, and the device may tear or separate, creating a risk of blood clot embolization.

    Product
    WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0403-2022·2021-12-29

    Hemashield Gold Knitted Bifurcated Vascular Graft Mislabeling Recall

    Maquet Cardiovascular is recalling Hemashield Gold vascular grafts due to probable mislabeling. A different graft product may have been packaged in the carton.

    Product
    Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0401-2022·2021-12-29

    Wright Medical CHARLOTTE MTP Hex Screw Recall: Incorrect Product in Packaging

    Wright Medical recalled 22 units of CHARLOTTE MTP Hex Screws with incorrect product in packaging. Affected lots 02010697711582590 and 02010697711582591 were distributed to surgical facilities in the US, Canada, Australia, Spain, UK, and Chile.

    Product
    Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE Lisfranc Reconstruction System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0293-2022·2021-12-29

    Give and Go Vanilla Cupcakes Recalled for Potential Metal Contamination

    Give and Go is recalling two-bite vanilla cupcakes nationwide due to potential metal contamination in the product. Consumers should stop using affected units and contact the manufacturer.

    Product
    two-bite vanilla cupcakes 10 oz. UPC 7 70981 03460 7 Horneaditos cupcake de vainilla 10 oz. UPC 7 70981 04125 4
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0314-2022·2021-12-29

    Favorite Day Bakery Frosted Sugar Cookies Recalled for Potential Metal

    GIVE AND GO is recalling Favorite Day Bakery Frosted Sugar Cookies (13.5 oz., UPC 0 85239 41050 9) distributed nationwide due to potential metal contamination in the product.

    Product
    Favorite Day Bakery Frosted Sugar Cookies 13.5 oz. UPC 0 85239 41050 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0317-2022·2021-12-29

    Kimberley's Bakeshoppe Sugar Cookies Recalled for Potential Metal Contamination

    GIVE AND GO is recalling Kimberley's bakeshoppe vanilla mini Frosted soft Sugar Cookies (9.4 oz., UPC 7 70981 30310 9) due to the potential for metal in the product. The recall affects approximately 1,142,754 retail units distributed nationwide.

    Product
    Kimberley's bakeshoppe vanilla mini Frosted soft Sugar Cookies 9.4 oz. UPC 7 70981 30310 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0397-2022·2021-12-29

    VirtuTRAX Instrument Navigator Sensor May Fail to Tighten Properly

    Civco Medical Instruments is recalling VirtuTRAX Instrument Navigator sensors because they may fail to tighten properly onto surgical instruments. This functional defect could affect safe use during medical procedures.

    Product
    VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0291-2022·2021-12-29

    Wondershop Vanilla Mini Cupcakes Recalled for Metal Contamination

    GIVE AND GO is recalling Wondershop at Target vanilla mini cupcakes due to potential metal contamination in the product. Affected units were distributed nationwide.

    Product
    Wondershop at Target vanilla mini cupcakes 10 oz. UPC 0 85239 03474 3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0402-2022·2021-12-29

    Nurse Call Communication System Components May Fail to Reboot

    Hill-Rom's NaviCare and Voalte nurse call communication systems may experience an unrecoverable software error causing components to fail reboot cycles and become non-functional, requiring replacement.

    Product
    These are communication systems, labeled as: a. NaviCare Nurse Call, Part Numbers: 3.6, 3.7, 3.9 b. Voalte Nurse Call, Part Number 4.0 *Product was rebranded from NaviCare to Voalte in 2020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0297-2022·2021-12-29

    Cupcakes Recalled for Potential Metal Contamination

    Two cupcake products sold nationwide are being recalled due to potential metal contamination. Affected consumers should stop consuming the products and contact the manufacturer for a refund.

    Product
    two-bite vanilla & chocolate cupcakes 20 oz. UPC 7 70981 03408 9 Favorite Day Bakery chocolate & vanilla mini cupcakes 10 oz. UPC 0 85239 12580 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0301-2022·2021-12-29

    Pumpkin Spice Mini Cupcakes Recalled for Potential Metal Contamination

    GIVE AND GO is recalling three brands of Pumpkin Spice mini cupcakes sold nationwide due to potential metal in the product. Consumers should not eat the affected cupcakes.

    Product
    Signature Select Pumpkin Spice mini cupcakes 10 oz. UPC 0 21130 98478 7 Bake Shop Pumpkin Spice mini cupcakes 10 oz. UPC 4 09910 02729 56 two-bite Pumpkin Spice cupcakes 10 oz. UPC 7 70981 05551 0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0300-2022·2021-12-29

    Carrot Cake Cupcakes Recalled for Potential Metal Contamination

    GIVE AND GO is recalling two carrot cake cupcake products nationwide due to the potential presence of metal in the product. Consumers should not consume affected lots and should contact the manufacturer or return the product to the place of purchase.

    Product
    two-bite carrot cake cupcakes 10 oz. UPC 7 70981 05525 1 Kimberley's bakeshoppe carrot cake filled gourmet cupcakes 11.5 oz. UPC 7 70981 31026 8
    Category
    Food
    Distribution
    Distributed nationwide