The Recall Desk

State

American Samoa product recalls

73,218 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.

What the numbers show

Total
25
Critical
1
Severe
5
Most recent
2026-09-09

Of the 25 recalls naming American Samoa we have scored against our rubric, 1 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 5 (20%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17376–17400 of 73243

  • HighFDA (Devices)·Z-1015-2023·2023-02-01

    Medical Device Manufacturer Recalls VAD Drive Kits With Expired Component

    Medline Industries is recalling 1,050 kits of Centurion Medical Products Silver Antimicrobial VAD Drive due to expired components. Affected kits were distributed across New York, Indiana, Florida, New Jersey, and Illinois.

    Product
    CENTURION MEDICAL PRODUCTS, SILVER ANTIMICROBIAL VAD DRIVE, REF DT18760
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0238-2023·2023-02-01

    Pharmacy Innovations Testosterone Injectables and Ophthalmic Products Recalled for Sterility Concerns

    Pharmacy Innovations is recalling multiple testosterone injectable and ophthalmic formulations nationwide due to insanitary facility conditions that prevent assurance of sterile manufacturing.

    Product
    TESTOSTERONE 3% (4GM TUBE) OPHTH OINTME TESTOSTERONE CYP/ANASTROZOLE-GS OIL- 200MG/0.5MG/ML (3.5ML VIAL) INJECTABLE TESTOSTERONE CYP/ANASTROZOLE-GS OIL- 200MG/1MG/ML (1.5ML VIAL) INJECTABLE TESTOSTERONE CYP/ANASTROZOLE-GS OIL- 200MG/1MG/ML (3ML VIAL) INJECTABLE TESTOSTERONE…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0204-2023·2023-02-01

    Edetate Disodium Ophthalmic Solution Recalled for Sterility Concerns

    Pharmacy Innovations is recalling Edetate Disodium 1% ophthalmic solution nationwide due to insanitary facility conditions that compromised sterility assurance. No illnesses have been reported.

    Product
    EDETATE DISODIUM (VET) 1% (3ML droptainer) OPH Solution, Rx Only, Pharmacy Innovations, 2936 W 17th St., Erie, PA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0178-2023·2023-02-01

    Sterile water injection vials recalled for trace product carryover risk

    Nephron Pharmaceuticals recalls approximately 389,730 vials of sterile water for injection nationwide due to potential product carryover from manufacturing deviations. No illnesses have been reported.

    Product
    STERILE WATER — STERILE WATER (STERILE WATER)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0207-2023·2023-02-01

    Injectable Ethyl Alcohol 95% Recalled Due to Sterility Assurance Concerns

    Pharmacy Innovations is recalling Ethyl Alcohol 95% (5ML vial) Injectable nationwide because FDA inspection revealed insanitary conditions at the manufacturing facility that compromise sterility assurance.

    Product
    Ethyl Alcohol 95% (5ML vial) Injectable, Rx Only, Pharmacy Innovations, 2936 W 17th St., Erie, PA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0234-2023·2023-02-01

    Injectable Prostaglandin E1 Multiple Strengths Recalled for Sterility Concerns

    Pharmacy Innovations is recalling multiple strengths of injectable Prostaglandin E1 nationwide due to lack of sterility assurance. FDA inspection found insanitary conditions at the manufacturing facility.

    Product
    PROSTAGLANDIN (PE1) 45MCG (1ML VIAL) INJECTABLE PROSTAGLANDIN E1 17MCG/ML (1ML VIAL) INJECTABLE PROSTAGLANDIN E1 20MCG/ML (1ML VIAL) INJECTABLE PROSTAGLANDIN E1 22.5MCG/ML (1ML VIAL) INJECTABLE PROSTAGLANDIN E1 23MCG/ML (1ML VIAL) INJECTABLE PROSTAGLANDIN E1 30MCG/ML (1ML VIAL)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0192-2023·2023-02-01

    Albuterol Inhalation Solution Recalled for Lack of Sterility Assurance

    Pharmacy Innovations is recalling nationwide Albuterol 0.083% inhalation solution in 3ML tubes due to insanitary manufacturing facility conditions that compromise sterility assurance.

    Product
    Albuterol (PF/SULFURIC ACID/DYE FREE) - 3ML tube - 0.083% Inhalation Solution, Rx Only, Pharmacy Innovations, 2936 W 17th St., Erie, PA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0214-2023·2023-02-01

    Pharmacy Innovations Recalls Heparin Irrigation Solution Due to Sterility Concerns

    Pharmacy Innovations is recalling a heparin-lidocaine irrigation solution nationwide due to lack of sterility assurance. FDA inspection found insanitary conditions at the manufacturing facility.

    Product
    HEPARIN/LIDO HCL/SODIUM BICARB 100U/2MG/16.8MG/ML (20ML SYRINGE) IRRIGATION, Rx Only, Pharmacy Innovations, 2936 W 17th St., Erie, PA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0211-2023·2023-02-01

    FDA Recalls Injectable Glycerin 72% Due to Sterility Assurance Failure

    Pharmacy Innovations is recalling Injectable Glycerin 72% (15mL vials) nationwide due to lack of sterility assurance discovered during FDA facility inspection.

    Product
    GLYCERIN 72% (W/V) (15ML VIAL) INJECTABLE, Rx Only, Pharmacy Innovations, 2936 W 17th St., Erie, PA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1020-2023·2023-02-01

    AirQ3 Intubating Laryngeal Airway Recall: Orogastric Tube Size Labeling Discrepancy

    SunMed is recalling 43,290 AirQ3 Self Pressurizing Intubating Laryngeal Airways due to a sizing discrepancy between device labeling and actual channel dimensions. Clinicians may need to use a smaller-diameter gastric catheter than indicated.

    Product
    AirQ3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Size REF Number 0.0 60005 0.5 60055 1.0 60105 1.5 60155 2.0 60205 3.0 60305 4.0 60405
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0176-2023·2023-02-01

    Drug Recall: S2 Racepinephrine Inhalation Solution Short Fill

    Nephron Sc Inc recalls approximately 925,920 vials of S2 Racepinephrine Inhalation Solution due to short fill. Affected lots may contain less medication than labeled.

    Product
    S2 — S2 (RACEPINEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0170-2023·2023-02-01

    Metoprolol Succinate Tablets Recalled for Failed Dissolution Specification

    Ascend Laboratories is recalling 6,336 bottles of Metoprolol Succinate Extended-Release Tablets, 50 mg, distributed nationwide and in Puerto Rico, due to failed dissolution specification.

    Product
    METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE ER TABLETS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1019-2023·2023-02-01

    Air-Q3 intubating laryngeal airway size labeling discrepancy between IFU and device

    SunMed's Air-Q3 intubating laryngeal airway devices have a discrepancy between the Instructions For Use and the printed text on the device regarding orogastric tube sizes, which could cause confusion when placing gastric catheters.

    Product
    Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Size REF Number 0.0 50005 0.5 50055 1.0 50105 1.5 50155 2.0 50205 3.0 50305 4.0 50405
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0174-2023·2023-02-01

    Clobetasol Propionate Cream recalled due to subpotent drug

    Lupin Pharmaceuticals is recalling Clobetasol Propionate Cream 0.05% nationwide because stability testing revealed insufficient active ingredient in the affected lot.

    Product
    CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·003-2023·2023-01-31

    Conagra Recalls Canned Meat and Poultry Due to Packaging Defect

    Conagra Brands is recalling approximately 2.6 million pounds of canned meat and poultry products due to a packaging defect that could allow contamination.

    Product
    ConAgra Brands, Inc. — Conagra Brands Recalls Canned Meat and Poultry Products Due to Possible Packaging Defect
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V038000·2023-01-31

    2022–2023 Hyundai Santa Cruz and Tucson roof moldings may detach

    Hyundai is recalling certain 2022 Santa Cruz and 2023 Santa Cruz vehicles, as well as 2022 Tucson vehicles, because the roof moldings may detach and become a road hazard.

    Product
    HYUNDAI — HYUNDAI TUCSON, SANTA CRUZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·001-2023·2023-01-29

    Daniele International Recalls Ready-to-Eat Sausage Products Due to Listeria Risk

    Daniele International LLC is recalling approximately 69,255 pounds of ready-to-eat sausage products that may be contaminated with Listeria monocytogenes.

    Product
    Daniele Operating, LLC - Stedagio — Daniele International LLC Recalls Ready-to-Eat Sausage Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V035000·2023-01-29

    2023 Kia Telluride Side Air Bag Wire Harness Damage Recall

    Kia is recalling certain 2023 Telluride vehicles because manufacturing errors may have damaged the second row seat side air bag wire harnesses, preventing deployment in a crash.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V034000·2023-01-27

    Bentley Recalls 2020 Continental GT Models Due to Fire Risk

    Bentley is recalling 2020 Continental GT and GTC vehicles because liquid entering the coolant pump may cause an electrical short circuit, increasing the risk of a vehicle fire.

    Product
    BENTLEY — BENTLEY CONTINENTAL GT, CONTINENTAL GT CABRIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V033000·2023-01-27

    Porsche Panamera coolant pump electrical short circuit increases fire risk

    Porsche is recalling certain 2017-2021 Panamera models because humidity can enter the external coolant pump, causing an electrical short circuit that increases the risk of vehicle fire. Dealers will replace the pump and inspect connections at no cost.

    Product
    PORSCHE — PORSCHE PANAMERA 4S, PANAMERA TURBO, PANAMERA TURBO EXECUTIVE, PANAMERA 4S SPORT TURISMO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·23V032000·2023-01-27

    2023 Winnebago Revel: incorrect tire size on safety label

    Certain 2023 Winnebago Revel camper vans have an incorrect tire size listed on the Tire and Loading Information Label (R16 instead of R17). Installing the wrong tires based on this incorrect information could increase the risk of a crash.

    Product
    WINNEBAGO — WINNEBAGO REVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23107·2023-01-26

    ZLINE Gas Ranges Recalled Due to Carbon Monoxide Emission Hazard

    ZLINE is recalling about 30,000 gas ranges (30-inch, 36-inch, and 48-inch models) because the oven compartment can emit dangerous levels of carbon monoxide, posing a serious risk of injury or death. Consumers should stop using the oven immediately until repaired.

    Product
    ZLINE 30-inch, 36-inch and 48-inch RG gas ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide