The Recall Desk

State

American Samoa product recalls

73,722 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
9
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 9 (36%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30951–30975 of 73747

  • ModerateFDA (Devices)·Z-0578-2020·2019-12-04

    Boston Scientific Recalls Guidezilla II Catheters Due to Missing Coating

    Boston Scientific is recalling Guidezilla II Guide Extension Catheters because they may lack a hydrophilic coating, potentially affecting device performance.

    Product
    Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide. Packaged in the following sizes: 1. REF/Catalog No. H7493933515060, 6F; 2. REF/Catalog No H7493933515070, 7F.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0582-2020·2019-12-04

    Bard PowerPort isp M.R.I. Implantable Port Recalled for Incorrect Sheath Size

    Bard Peripheral Vascular Inc is recalling 900 units of PowerPort isp M.R.I. Implantable Ports because they were packaged with the incorrect introducer sheath size.

    Product
    PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0575-2020·2019-12-04

    Avantor Recalls Potassium Phosphate Bulk Chemical for Excess Iron Content

    Avantor Performance Materials Inc is recalling bulk Potassium Phosphate, Monobasic, Crystal due to failed stability specifications for iron content.

    Product
    Potassium Phosphate, Monobasic, Crystal, NF, Multi-Compendial, Bulk Pharmaceutical Chemical, packaged in a) 500G glass bottles, product number 3248-01, NDC 10106-3248-1; b) 2.5KG glass bottles, product number 3248-05, NDC 10106-3248-2; c) 12KG pails, product number 3248-07, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0522-2020·2019-12-04

    AuroMedics Recalls Amiodarone Hydrochloride Injection Due to Visible Particulate Matter

    AuroMedics Pharma LLC is recalling Amiodarone Hydrochloride Injection vials due to the presence of visible particulate matter (crystallization). The affected lots were distributed nationwide in the US.

    Product
    AMIODARONE HYDROCHLORIDE — AMIODARONE HYDROCHLORIDE (AMIODARONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0193-2020·2019-12-04

    Merical Recalls Leader Advanced Probiotic Due to Incorrect Labeling

    Merical, LLC is recalling Leader Advanced Probiotic capsules because the label lists the wrong probiotic blend. Consumers should stop using the product.

    Product
    Leader Advanced Probiotic with 6 Probiotic Strains and 20 billion Live Cultures. 30 capsules Item Number: CARD40359, Product Number: 907019, UPC Code: 096295136654
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0521-2020·2019-12-04

    AuroMedics Recalls Amiodarone Hydrochloride Injection Due to Visible Particulate Matter

    AuroMedics Pharma LLC is recalling Amiodarone Hydrochloride Injection vials due to the presence of visible particulate matter (crystallization). The affected lots were distributed nationwide in the US.

    Product
    AMIODARONE HYDROCHLORIDE — AMIODARONE HYDROCHLORIDE (AMIODARONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·19V858000·2019-12-03

    Moto Guzzi Recalls 2020 V85 TT Motorcycles for Footrest Defect

    Piaggio is recalling 399 2020 Moto Guzzi V85 TT motorcycles because footrest mounting clips may break, causing the footrest to fall off and create a road hazard.

    Product
    MOTO GUZZI — MOTO GUZZI V85 TT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E082000·2019-12-03

    Zamzow Aero Easy Cover tarping pawl assembly recall issued

    Zamzow is recalling one Aero Easy Cover tarping pawl assembly because a missing weld may cause the part to separate, increasing injury risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E081000·2019-12-02

    IMT Standen Recalls Leaf Spring Assemblies for Trailer Suspension Defects

    IMT Standen is recalling certain leaf spring assemblies for trailers because they may crack and break, posing a road hazard and increasing crash risk.

    Product
    SUSPENSION:REAR:SPRINGS:LEAF SPRING ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V856000·2019-12-02

    Subaru Recalls 2019 Models for Engine Valve Separation Risk

    Subaru is recalling 51,613 2019 Crosstrek, Forester, and Ascent vehicles because a PCV valve can separate, causing loss of power and increasing crash risk.

    Product
    SUBARU — SUBARU CROSSTREK, ASCENT, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V857000·2019-12-02

    Moto Guzzi Recalls 2020 V85 TT Motorcycles for Oil Leak Hazard

    Piaggio is recalling 2020 Moto Guzzi V85 TT motorcycles because a final drive seal may leak oil onto the rear tire, increasing crash risk.

    Product
    MOTO GUZZI — MOTO GUZZI V85 TT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0468-2020·2019-11-27

    Altaire Recalls Up & Up Lubricating Eye Drops for Sterility Concerns

    Altaire Pharmaceuticals is recalling Up & Up Intensive Relief Lubricating Eye Drops due to a lack of assurance of sterility.

    Product
    TRP/ TARGET up & up intensive relief lubricating eye drop, 10 mL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0368-2020·2019-11-27

    Altaire Recalls Equate Night & Day Restore Tears Lubricant Eye Pack

    Altaire Pharmaceuticals is recalling Equate Night & Day Restore Tears Lubricant Eye Pack due to a lack of assurance of sterility.

    Product
    Equate Night & Day Restore Tears Lubricant Eye Pack W-M item #: 567368000, Package Size: 3.5g and 15mL, Distributed by: Wal-Mart Stores Inc., Bentonville, AR 72716, NDC 49035-883-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0439-2020·2019-11-27

    Altaire ActivEyes Lubricant Eye Ointment Recalled for Sterility Concerns

    Altaire Pharmaceuticals is recalling ActivEyes Lubricant Eye Ointment due to a lack of assurance of sterility.

    Product
    ActivEyes Lubricant Eye Ointment Preservative Free, Product Size: 3.5 gram, Manufactured by: Altaire Pharmaceuticals, Inc. Aquebogue, NY 11931,NDC 59390-189-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0486-2020·2019-11-27

    Altaire Recalls Grandall Oftal-Mycin Ophthalmic Ointment Due to Sterility Concerns

    Altaire Pharmaceuticals is recalling Grandall Oftal-Mycin Ophthalmic Ointment because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide.

    Product
    Grandall Oftal-Mycin Ophthalmic Ointment, Product Size: 3.5 g
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0367-2020·2019-11-27

    Altaire Recalls Equate Eye Ointment Due to Sterility Concerns

    Altaire Pharmaceuticals is recalling Equate Restore PM Nighttime Lubricant Eye Ointment because the product may not be sterile.

    Product
    Equate Restore PM Nighttime Lubricant Eye Ointment, Sterile, Net Wt. 0.125 oz. (3.5g), Distributed by: Walmart Stores Inc., Bentonville, AR 72716, W-M item #551282425, NDC 49035-191-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0463-2020·2019-11-27

    Altaire Recalls Women's Tear Stimulation Dry Eye Drops for Sterility Concerns

    Altaire Pharmaceuticals is recalling Natural Ophthalmics Women's Tear Stimulation Dry Eye Drops due to a lack of assurance of sterility.

    Product
    Natural Ophthalmics Women's Tear Stimulation Dry Eye Drops, 15 mL, NDC 68770-103-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0435-2020·2019-11-27

    Altaire Pharmaceuticals Recalls iSolutions Nano Tears XP Due to Sterility Concerns

    Altaire Pharmaceuticals is recalling iSolutions Nano Tears XP eye drops because the company cannot guarantee the product is sterile.

    Product
    iSolutions Nano Tears XP Clear Emollient Lubricant Gel Drops Moderate Sterile, 1/3 FL OZ (10 mL), Mfd. By: Altaire Pharmaceuticals, Inc. Aquebogue, NY 11931, NDC 59390-143-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0366-2020·2019-11-27

    Altaire Recalls Equate Eye Gel Due to Sterility Concerns

    Altaire Pharmaceuticals is recalling Equate Comfort Gel Lubricant Eye Gel because the product lacks assurance of sterility.

    Product
    Equate Comfort Gel Lubricant Eye Gel Twin Pack W-M item #: 552374319, Package Size: 2 x 15 mL, Distributed by: Walmart Inc., Bentonville, AR 72716, NDC 49035-197-49
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0434-2020·2019-11-27

    Altaire Pharmaceuticals Recalls iSolutions Nano Tears Due to Sterility Concerns

    Altaire Pharmaceuticals is recalling iSolutions Nano Tears TF Clear Emollient Lubricant Gel Drops because the product may not be sterile.

    Product
    iSolutions Nano Tears TF Clear Emollient Lubricant Gel Drops Tear Film Replenishment Mild Sterile, 0.5 FL OZ (15 mL), Manufactured by: Altaire Pharmaceuticals, Inc. Aquebogue, NY 11931, NDC 59390-142-13
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0440-2020·2019-11-27

    Altaire Recalls OCuSOFT Homatropine Hydrobromide Ophthalmic Solution Due to Sterility Concerns

    Altaire Pharmaceuticals is recalling OCuSOFT Homatropine Hydrobromide Ophthalmic Solution, 5%, due to a lack of assurance of sterility. The recall covers 81,403 units distributed nationwide.

    Product
    OCuSOFT Homatropine Hydrobromide Ophthalmic Solution, 5%, 5 mL, Rx only, Manufactured for Ocusoft, Inc, Rosenberg, TX 77471, Mfd. by Altaire Pharmaceuticals, Inc, Aquebogue, NY 11931 NDC 54799-431-05
    Category
    Drug
    Distribution
    Distributed nationwide