The Recall Desk

State

American Samoa product recalls

73,106 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 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13651–13675 of 73131

  • ModerateFDA (Devices)·Z-0245-2024·2023-11-15

    Disposable surgical forceps recalled for incorrect expiration date labeling

    Stryker recalls disposable Spetzler-Malis Bipolar forceps due to expiration date labeling error. Labels show 54-month shelf life but actual shelf life is 36 months.

    Product
    Disposable Spetzler-Malis Bipolar forceps, 18CM IM DISP BAYONET 0.5MM TIP, Catalog Number 6770-180-005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0098-2024·2023-11-15

    Oxybutynin Extended-Release Tablets Recalled for Failed Dissolution Test Results

    Zydus Pharmaceuticals is recalling Oxybutynin Extended-Release Tablets (15 mg) after dissolution testing showed out-of-specification results at the 6-month mark. No illnesses have been reported.

    Product
    OXYBUTYNIN — OXYBUTYNIN (OXYBUTYNIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0092-2024·2023-11-15

    Ranolazine Extended-Release Tablets Recalled for Failed Dissolution Specifications

    Glenmark Pharmaceuticals is recalling 16,944 bottles of Ranolazine 500mg tablets nationwide due to failed dissolution specifications. Tablets may not dissolve properly, potentially affecting drug efficacy.

    Product
    RANOLAZINE — RANOLAZINE (RANOLAZINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0089-2024·2023-11-15

    Hydrocortisone and Acetic Acid Otic Solution recalled for failed specifications

    Taro Pharmaceuticals recalls 11,196 bottles of Hydrocortisone and Acetic Acid Otic Solution nationwide due to failed quality specifications including out-of-spec impurities and lower-than-established assay levels discovered during stability testing.

    Product
    HYDROCORTISONE AND ACETIC ACID — HYDROCORTISONE AND ACETIC ACID (HYDROCORTISONE AND ACETIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0242-2024·2023-11-15

    Disposable Surgical Forceps Recalled for Incorrect Expiration Date Labeling

    Stryker Corporation is recalling 2,321 units of Disposable Spetzler-Malis Bipolar forceps due to an error in the product label's expiration date. The label indicates a 54-month shelf life when the actual shelf life is 36 months.

    Product
    Disposable Spetzler-Malis Bipolar forceps, 23CM SM DISP BAYONET 0.5MM TIP, Catalog Number 6760-230-005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0248-2024·2023-11-15

    Disposable Bipolar Forceps Shelf Life Labeling Error Stryker

    Stryker recalls disposable Spetzler-Malis bipolar forceps due to incorrect shelf life labeling. The label states 54 months but the actual shelf life is 36 months.

    Product
    Disposable Spetzler-Malis Bipolar forceps, 20CM IM DISP BAYONET 0.5MM TIP, Catalog Number 6770-200-005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0256-2024·2023-11-15

    Stryker surgical forceps recall due to incorrect expiration date labeling

    Stryker Corporation is recalling Spetzler-Malis Bipolar forceps due to incorrect shelf-life labeling. The devices are labeled with a 54-month shelf life but actually expire after 36 months.

    Product
    Disposable Spetzler-Malis Bipolar forceps, 23CM SLM DISP BAYONET 1.0MM, Catalog Number 6780-230-010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0097-2024·2023-11-15

    Zydus oxybutynin extended-release tablets recalled nationwide for failed stability testing

    Zydus Pharmaceuticals is recalling specific lots of oxybutynin chloride extended-release 10 mg tablets nationwide due to out-of-specification dissolution test results at the 6-month stability timepoint. The affected tablets may not release medication properly.

    Product
    OXYBUTYNIN — OXYBUTYNIN (OXYBUTYNIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0091-2024·2023-11-15

    Antifungal Powder Recalled Due to Low Active Ingredient Content

    Medline Industries is recalling REMEDY Antifungal powder nationwide because it contains insufficient miconazole nitrate (the active ingredient). The product was shipped before assay testing was complete.

    Product
    REMEDY ANTIFUNGAL — REMEDY ANTIFUNGAL (MICONAZOLE NITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0253-2024·2023-11-15

    Surgical forceps recalled due to mislabeled shelf life

    Stryker Corporation is recalling Disposable Spetzler-Malis Bipolar forceps due to a labeling error showing an incorrect expiration date. The label states a 54-month shelf life when the actual shelf life is 36 months.

    Product
    Disposable Spetzler-Malis Bipolar forceps, 20CM SLM DISP BAYONET 1.0MM, Catalog Number 6780-200-010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V768000·2023-11-14

    Lonestar Recalls 2021-2023 SV Electric S22 Tractors for Fire Risk

    Lonestar is recalling 2021-2023 SV Electric S22 terminal tractors because a software defect may prevent detection of high-voltage battery malfunctions, increasing fire risk.

    Product
    LONESTAR — LONESTAR SV ELECTRIC S22
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E088000·2023-11-14

    Driver Air Bag Clockspring Recall for Potential Deactivation

    BCS Automotive recalls steering column control modules that may fail and deactivate driver air bags, increasing crash injury risk.

    Product
    AIR BAGS:FRONTAL:DRIVER CLOCKSPRING/SPIRAL CASSETTE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V751000·2023-11-13

    Honda Recalls Acura and Honda Vehicles for Engine Bearing Defect

    Honda is recalling specific Acura and Honda models because a manufacturing error may cause engine bearing wear, leading to stalling or fire.

    Product
    ACURA — ACURA, HONDA TLX, MDX, PILOT, RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V766000·2023-11-13

    Triple E RV Recalls 2023-2024 Wonder Motorhomes Due to Fire Risk

    Triple E Recreational Vehicles is recalling 2023-2024 Wonder motorhomes because damaged wire insulation on the 120-volt air conditioner line may cause electrical arcing and increase the risk of a fire.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V764000·2023-11-13

    Terberg Terminal Tractor Recall for Loose Steering Axle Nuts

    Terberg Benschop B.V. is recalling one 2022 YT193 terminal tractor because non-self-locking flange nuts on the steering front axle may come loose, potentially causing a loss of steering or braking.

    Product
    TERBERG BENSCHOP B.V. — TERBERG BENSCHOP B.V. TERMINAL TRACTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V763000·2023-11-11

    Nova Bus LFS Transit Buses Recalled for HVAC Unit Bracket Failure

    Nova Bus (US) Inc. is recalling 2020–2023 LFS transit buses because mounting brackets for the HVAC unit could fail, causing the unit to detach and create a road hazard. Free repairs are available through Nova Bus customer service.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V762000·2023-11-11

    2022 Nova Bus LFS Transit Buses Recalled for Turn Signal Failure

    Nova Bus is recalling certain 2021-2023 LFS transit buses due to defective turn signal wiring that may fail intermittently, increasing crash risk. Free repairs are available.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V761000·2023-11-10

    Prevost Motor Coaches Recalled for Fire Risk in Grid Heater System

    Prevost Car (US) Inc. is recalling 204 certain 2023-2024 H3-45 and X3-45 VIP motor coaches due to loose grid heater cable connections that can cause the relay to overheat, increasing fire risk.

    Product
    PREVOST — PREVOST X3-45, H3-45 VIP, X3-45 VIP, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V759000·2023-11-10

    Solar Panels May Detach from Thor Rize and Scope Motorhomes

    Thor Motor Coach is recalling 2021-2024 Rize and Scope motorhomes because the solar panel frame may fracture at the mounting bolts and detach, creating a road hazard.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH SCOPE, RIZE, redundant RIZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V754000·2023-11-09

    2024 Subaru Impreza Front Driveshaft Assembly Defect Recall

    Subaru is recalling 2024 Impreza vehicles because the front driveshaft assembly may develop cracks and break, potentially causing loss of drive power or vehicle rollaway, increasing crash risk.

    Product
    SUBARU — SUBARU FORESTER, WRX, IMPREZA, CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24023·2023-11-09

    Twin-Star International Recalls Infrared Quartz Electric Fireplaces for Fire Hazard

    Twin-Star International is recalling approximately 14,670 Style Selections 42-inch-wide Infrared Quartz Electric Fireplaces sold at Lowe's because the units can overheat and pose a fire hazard. Twenty-four reports of overheating, fire, or smoke incidents have been received, including two reports of property damage.

    Product
    Style Selections 42-inch-wide Infrared Quartz Electric Fireplaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide