The Recall Desk

State

Hawaii product recalls

72,907 recalls have nationwide distribution and so reach Hawaii. 2,766 additional recalls listed Hawaii specifically in their distribution scope.

What the numbers show

Total
2,766
Critical
333
Severe
567
Most recent
2026-09-09

Of the 2,766 recalls naming Hawaii we have scored against our rubric, 333 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 567 (20%) are Severe.

These figures cover only the 2,766 recalls whose distribution notice names Hawaii specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1476–1500 of 75673

  • HighFDA (Drugs)·D-0561-2026·2026-06-10

    Good Neighbor Pharmacy 1000 mg antacid tablets contain metallic particles

    Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    ULTRA STRENGTH ANTACID ASSORTED FRUIT — ULTRA STRENGTH ANTACID ASSORTED FRUIT (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2301-2026·2026-06-10

    BD Pyxis Mini Main cabinets may overheat at fingerprint scanner

    BD Pyxis Mini Main medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 709 units affected.

    Product
    BD Pyxis Mini Main REF: 349 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0566-2026·2026-06-10

    CareOne ultra strength antacid tablets contain small metallic particles

    CareOne Ultra Strength Calcium Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    ULTRA STRENGTH ANTACID ASSORTED BERRIES — ULTRA STRENGTH ANTACID ASSORTED BERRIES (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0562-2026·2026-06-10

    Casey's extra strength antacid tablets contain small metallic particles

    Casey's Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles in the tablets.

    Product
    Extra strength Antacid Calcium Carbonate 750 mg, chewable tablets, 96-count bottle, DISTRIBUTED BY CASEY'S MARKETING COMPANY, ANKENY, IA 50521, UPC: 0 98437 24361 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0996-2026·2026-06-10

    Imitation crab and shrimp sriracha salad does not declare pollock

    Albertsons store-made Imitation Crab and Shrimp Salad Sriracha is being recalled because the contains statement does not declare pollock. 15 units are affected.

    Product
    UPC 23285600000 IMITATION CRAB AND SHRIMP SALAD SRIRACHA This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1019-2026·2026-06-10

    Albertsons chicken caesar salad does not declare anchovy allergen

    Albertsons store-made chicken caesar salad is being recalled because the contains statement does not declare anchovy. 328 units are affected.

    Product
    UPC 24512800000 SALAD CHICKEN CAESAR UPC 29854600000 Kitchen SALAD CHICKEN CAESAR This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2307-2026·2026-06-10

    Aligned Medical fluids kits contain recalled lidocaine injection

    Aligned Medical AMS16835 Fluids Kits are being recalled because they include Lidocaine Hydrochloride Injection, USP that was recalled by a supplier for quality issues.

    Product
    Aligned Medical AMS16835 Fluids Kit RX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1073-2026·2026-06-10

    Albertsons berry and salmon salad omits salmon and walnut declarations

    Albertsons store-made Fresh Berry & Salmon Salad is being recalled because the contains statement does not declare salmon and walnut. 90 units are affected.

    Product
    UPC 21477700000 Ready Meals SALAD FRESH BERRY & SALMON SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1014-2026·2026-06-10

    Albertsons cajun seafood salad does not declare crab and pollock

    Albertsons store-made Cajun Seafood Salad is being recalled because the contains statement does not declare crab and pollock. 110 units are affected.

    Product
    UPC 29477800000 Ready Meals SALAD SEAFOOD CAJUN SS COLD UPC 29477600000 SALAD SEAFOOD CAJUN FS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0961-2026·2026-06-10

    Cakerie strawberry shortcake triangles do not declare hazelnut allergen

    Albertsons store-made Cake Cakerie Strawberry Shortcake Triangle is being recalled because the contains statement does not declare hazelnut. 71 units are affected.

    Product
    UPC 25139500000 Cake Cakerie Strawberry Shortcake Triangle. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1024-2026·2026-06-10

    Albertsons pad thai chicken meal does not declare anchovy

    Albertsons store-made Wok Pad Thai Chicken with Egg Roll is being recalled because the contains statement does not declare anchovy. 12 units are affected.

    Product
    UPC 21379600000 Ready Meals WOK PAD THAI CHICKEN WITH EGG ROLL SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0573-2026·2026-06-10

    H-E-B extra strength antacid tablets contain small metallic particles

    H.E.B Extra Strength Calcium Carbonate Antacid Tablets, 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    HEB EXTRA STREGTH ANTACID — HEB EXTRA STREGTH ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0977-2026·2026-06-10

    Albertsons Italian super sub sandwich does not declare pistachio

    Albertsons store-made Kitchen Sandwich Italian Super Sub is being recalled because the contains statement does not declare pistachio. 28 units are affected.

    Product
    UPC 21243500000 KITCHEN SANDWICH ITALIAN SUPER SUB SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2297-2026·2026-06-10

    BD Pyxis MedStation 4000 fingerprint scanner may overheat and burn

    The BD Pyxis MedStation 4000 medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis MedStation 4000 REF: 303 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1015-2026·2026-06-10

    Imitation Cajun crab seafood salad does not declare crab and pollock

    Albertsons store-made Seafood Salad Imitation Cajun Crab is being recalled because the contains statement does not declare crab and pollock. 53 units are affected.

    Product
    UPC 23114800000 SEAFOOD SALAD IMITATION CAJUN CRAB This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1035-2026·2026-06-10

    Albertsons large spring salad does not declare almond allergen

    Albertsons store-made Kitchen Salad Spring Large is being recalled because the contains statement does not declare almond. 25 units are affected.

    Product
    UPC 29787500000 KITCHEN SALAD SPRING LARGE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1032-2026·2026-06-10

    Albertsons pork meat pies do not declare anchovy allergen

    Albertsons store-made pork meat pies are being recalled because the contains statement does not declare anchovy. 790 units in total are affected.

    Product
    UPC 21176300000 MEAT PIE PORK 4CT SS COLD UPC 21025900000 PIE PORK FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0994-2026·2026-06-10

    Albertsons Twisted Bliss pretzel trays do not declare almond allergen

    Albertsons store-made Twisted Bliss Pretzel Tray is being recalled because the contains statement does not declare almond. Two units are affected.

    Product
    UPC 29344500000 TWISTED BLISS PRETZEL TRAY This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2282-2026·2026-06-10

    Neptune docking station shipped without verified electrical safety testing

    A Neptune Smart Docking Station is being recalled because it was not released from manufacturing and may not have completed required testing, leaving a potential shock risk.

    Product
    Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2274-2026·2026-06-10

    Ivenix infusion pump cassette loading levers may break

    The Large Volume Pump of the Ivenix Infusion System is being recalled because of the potential for the Cassette Loading Lever to break. 18,444 installed bases are affected.

    Product
    The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1038-2026·2026-06-10

    Albertsons kale berry feta salad does not declare walnut

    Albertsons store-made Kale Berry Feta Salad is being recalled because the contains statement does not declare walnut. 31 units are affected.

    Product
    UPC 29472300000 SALAD KALE BERRY FETA FS COLD UPC 29472100000 Ready Meals SALAD KALE BERRY FETA SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0558-2026·2026-06-10

    Tums assorted fruit antacid tablets contain small metallic particles

    Tums Antacid Assorted Fruit tablets, calcium carbonate 1000 mg in 160-count bottles, are being recalled because of small metallic particles in the chewable tablets.

    Product
    HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC 3 07660 74610 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0991-2026·2026-06-10

    Albertsons 16-inch Italian sampler tray does not declare almond

    An Albertsons store-made 16-inch Italian sampler tray is being recalled because the contains statement does not declare almond. Nine units are affected.

    Product
    UPC 29153000000 SAMPLER TRAY ITALIAN 16 INCH This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2284-2026·2026-06-10

    Philips Azurion 3M12 Roadmap Pro may produce unusable dark images

    Philips Azurion 3M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide