The Recall Desk

State

American Samoa product recalls

73,096 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 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11551–11575 of 73121

  • HighFDA (Devices)·Z-1615-2024·2024-05-01

    LightStrike Blackout Curtains Recalled Due to Inadequate UV and Ozone Protection

    XENEX LightStrike Blackout Curtains are recalled due to inadequate protection against UV and ozone exposure. Bystanders in rooms during device operation may experience temporary skin reddening, eye irritation, nausea, and headache.

    Product
    LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-00024, used with the LightStrike Germ-Zapping Robots Models: PXUV4D, PXUV5D, LSMUV6-FT, or LSMUV6-SL, for whole room microbial reduction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0473-2024·2024-05-01

    Cloderm Cream Recalled for Manufacturer Quality Assurance Program Discontinuation

    EPI Health is recalling Cloderm cream due to discontinuation of the manufacturer's quality assurance program. This may result in products that do not meet specifications for identity, strength, purity, or quality.

    Product
    Cloderm (clocortolone pivalate) Cream, 0.1%, Rx Only, For Topical Use Only, Net Wt 45g, Manufactured for: EPI Health, LLC, Charleston, SC 29403, NDC 71403-804-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0474-2024·2024-05-01

    Minocycline Extended-Release Tablets Recalled for Manufacturing Quality Control Failure

    EPI Health is recalling minolira extended-release tablets due to manufacturer discontinuation of quality control programs affecting product identity, strength, and purity. The recall covers 12,808 bottles distributed nationwide.

    Product
    minolira (minocycline hydrochloride) extended-release tablets, 105mg 30-count Bottle, Rx Only, Mfg by: Dr Reddy's Laboratories Limited, INDIA, Manufactured for: EPI Health, LLC, Charleston, SC 29403, NDC 71403-101-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1625-2024·2024-05-01

    TRIDENTII HEMI Hip Implant Acetabular Shell Deburring Defect Recall

    Howmedica Osteonics is recalling the TRIDENTII HEMI CLUSTER54E hip implant due to excessive deburring on the acetabular shell edge that may affect implant performance. The recall involves 225 units distributed nationwide and internationally.

    Product
    TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-54E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1618-2024·2024-05-01

    Replacement Lead Wires Recalled for Risk of Treatment Delivery Failure

    EBI, LLC recalls 829 replacement lead wire assemblies (Part 1067724-2) distributed nationwide since May 1, 2023. Damaged wire sheaths may prevent therapeutic treatment signals from reaching electrodes, potentially delaying treatment.

    Product
    20" Lead Wires, Replacement Part Number: 1067724-2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1604-2024·2024-05-01

    Redux Electrolyte Creme Recalled for Low Viscosity Defect

    Parker Laboratories is recalling Redux Electrolyte Creme, a highly conductive medical electrolyte product, due to demonstrated low viscosity.

    Product
    Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0468-2024·2024-05-01

    Prescription Drug Recall: ABILIFY Tablets Due to Cross Contamination

    ABILIFY (aripiprazole) 15 mg tablets from lot AMS00223A are being recalled due to cross contamination with other products. The recall affects packages distributed nationwide.

    Product
    ABILIFY — ABILIFY (ARIPIPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1633-2024·2024-05-01

    3M Durapore Surgical Tape incorrectly labeled with extended shelf life

    Select lots of 3M Durapore Surgical Tape (Catalog Number 1538-118) were labeled with a 5-year shelf life when the actual shelf life is 3 years. The recall affects over 3.5 million rolls distributed worldwide.

    Product
    3M Durapore Surgical Tape, Catalog Number 1538-118
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0461-2024·2024-05-01

    Eyewash Solution Recalled for Manufacturing Compliance Deviations

    Honeywell Inc. is recalling FENDALL 2000 PURE FLOW eyewash solution due to Current Good Manufacturing Practice deviations. The recall affects 10,605 cartridges distributed nationwide in the USA and Canada with expiration dates through June 2025.

    Product
    FENDALL 2000 PURE FLOW — FENDALL 2000 PURE FLOW (PURIFIED WATER)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0465-2024·2024-05-01

    FUL-GLO Fluorescein Sodium Ophthalmic Strips Recalled for API Manufacturing Defect

    Nomax Inc recalls FUL-GLO Fluorescein Sodium Ophthalmic Strips (Lot 14776) nationwide due to API manufacturing specification failures. The active ingredient was not manufactured to current USP standards regarding unspecified impurities.

    Product
    FUL-GLO, Fluorescein Sodium Ophthalmic Strips USP 1 mg, 100 sterile strips per carton, Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-404-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0466-2024·2024-05-01

    Prescription medication Abilify recalled for cross contamination with other products

    Otsuka America Pharmaceutical is recalling certain lots of Abilify (aripiprazole) 5 mg tablets distributed nationwide due to cross contamination with other products. This is classified as a Class III recall.

    Product
    ABILIFY — ABILIFY (ARIPIPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1689-2024·2024-05-01

    Baxter Seprafilm Adhesion Barrier Recalled for Unapproved Distribution

    Baxter Healthcare is recalling Seprafilm Adhesion Barrier units (165 units, Lot DBYSEP046) that were distributed nationwide without FDA approval. Affected units distributed in LA, GA, IN, VA, FL, NY, and CA.

    Product
    Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V306000·2024-04-30

    Alfa Romeo Giulia Fuel Line Sensor Housing Recall

    Stellantis is recalling 2021 Alfa Romeo Giulia vehicles because a fuel line sensor housing may crack and leak fuel, increasing the risk of engine stall or fire.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V307000·2024-04-30

    Braun Ambulances Recalls 2023-2024 Models Due to Electrical Fire Risk

    Braun Ambulances is recalling 29 vehicles from 2023-2024 because a firmware defect can cause electrical circuits to overheat, increasing the risk of fire.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES EXPRESS PLUS TYPE I, CHIEF XL TYPE I, EXPRESS TYPE III, CHIEF XL TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V302000·2024-04-29

    MINI Cooper SE battery housing can admit water causing fire or stall

    BMW is recalling certain 2020-2024 MINI Hardtop 2 Door (Cooper SE) vehicles because the high voltage battery housing may not have been sealed properly, allowing water to enter the battery.

    Product
    MINI — MINI COOPER SE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V304000·2024-04-29

    Nissan Sentra driveshaft may unseat causing fluid leak and power loss

    Nissan is recalling certain 2024 Sentra vehicles because the front left driveshaft may not be fully seated in the CVT assembly, or may have a loose or missing retaining clip.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V303000·2024-04-29

    Alliance RV Recalls 2024 Avenue Travel Trailers Due to Wiring Defect

    Alliance RV is recalling 2024 Avenue travel trailers because an improperly wired inverter circuit could cause a breaker to overheat and increase fire risk.

    Product
    ALLIANCE RV — ALLIANCE RV AVENUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V305000·2024-04-29

    Reading Truck Equipment Recalls RM-78 Cranes Due to Taillight Height

    Reading Truck Body LLC is recalling 2022-2024 RM-78 crane bodies because taillights may be mounted too high, reducing visibility and increasing crash risk.

    Product
    READING TRUCK EQUIPMENT — READING TRUCK EQUIPMENT RM-78 CRANE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V299000·2024-04-29

    Highland Ridge RV Recalls Trailers Due to Overheating Circuit Board Fire Risk

    Highland Ridge RV is recalling 681 model year 2022-2023 trailers because an LED backlight circuit board may overheat, increasing the risk of a fire.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW OPEN RANGE, SILVERSTAR, MESA RIDGE XLT, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V301000·2024-04-29

    Motorhome cooktop control boards can overheat and cause fire

    Newmar is recalling certain 2022 Bay Star motorhomes because the LED backlight circuit board in the cooktop range may fail and overheat.

    Product
    NEWMAR — NEWMAR BAY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V300000·2024-04-29

    Starcraft Recalls 2023 GSL Fifth Wheel Trailers Due to Fire Risk

    Starcraft RV is recalling 2023 GSL fifth wheel trailers because the cooktop LED backlight circuit board may overheat, increasing the risk of a fire.

    Product
    STARCRAFT RV FW — STARCRAFT RV FW STARCRAFT GSL
    Category
    Vehicle
    Distribution
    Distributed nationwide