The Recall Desk

State

American Samoa product recalls

73,597 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 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29376–29400 of 73622

  • ModerateFDA (Devices)·Z-1544-2020·2020-04-01

    Medline Stick Sponge Presaturated W/PVP Recalled for Packaging Seal Voids

    Medline is recalling Stick Sponge Presaturated W/PVP units due to packaging seal voids that compromise sterility.

    Product
    Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1536-2020·2020-04-01

    Siemens Atellica CH Direct Bilirubin Assay Recalled for Positive Bias

    Siemens Healthcare Diagnostics is recalling Atellica CH Direct Bilirubin assays because they may show inaccurate results for patients taking eltrombopag.

    Product
    Atellica CH Direct Bilirubin_2 assay In vitro Diagnostic for the determination of direct bilirubin SMN: 11097532 - Product Usage: ADVIA DBIL_ 2 is for in vitro diagnostic use in the quantitative determination of direct bilirubin in human serum and plasma on the ADVIA¿ Chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1573-2020·2020-04-01

    Bard Vaccess CT Implantable Port Recall Due to Incorrect Tunneler Tip

    Bard Peripheral Vascular Inc is recalling 598 Vaccess CT Power-Injectable Implantable Ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.

    Product
    1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs, Ref: 7496000, UDI:(01)00801741027482 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The port system can be used for infusion of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0905-2020·2020-04-01

    Touchstone Essentials Super Greens Juice Recalled for Unapproved Herbicide

    Organic By Nature, Inc. is recalling Touchstone Essentials Super Greens Juice due to the presence of the unapproved herbicide Haloxyfop in an ingredient.

    Product
    Touchstone Essentials Super Greens Juice - Raspberry Apple; Premium Organic Superfood Juice Powder: Whole Food Dietary Supplement; Net Wt. 10.5 oz. (300 g) Plastic Bottle; Finished Product Item#: FTSGJRA300G Manufactured Exclusively for: Touchstone Essentials, Raleigh…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1571-2020·2020-04-01

    Bard PowerPort M.R.I. Implantable Port Catheter Recall for Incorrect Tunneler Tip

    Bard Peripheral Vascular Inc is recalling 878 PowerPort M.R.I. Implantable Port catheters because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.

    Product
    1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, REF: 1809600, UDI: (01)00801741027130 ; 2. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter Without Suture…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0898-2020·2020-04-01

    Organic By Nature Daily Fiber Blend Recalled for Unapproved Herbicide

    Organic By Nature is recalling Daily Fiber Blend - Caramel Apple Flavor because the flaxseed powder ingredient contains unapproved herbicide Haloxyfop.

    Product
    Daily Fiber Blend - Caramel Apple Flavor; Organic Plant Powder Mix for preparation of a fiber-rich drink, 540g Plastic Bottle, 180g Bio Bag Terra Pouch; Finished Product Item#: 2012E, 2012, 2012-P65, 2013, 2013-P65, 2016, 2016-P65 Brand names of: Platinum Health Europe…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1577-2020·2020-04-01

    BardPort M.R.I. Hard Base Implantable Port Recall Due to Incorrect Tunneler Tip

    Bard Peripheral Vascular Inc is recalling 151 BardPort M.R.I. Hard Base Implantable Ports because they may contain an incorrect tunneler barb tip, potentially prolonging surgical operations.

    Product
    BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter, Ref: 0604550, UDI: (01)00801741025860 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The port…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0895-2020·2020-04-01

    Organic By Nature Chia/Flax Boost Recalled for Unapproved Herbicide

    Organic By Nature is recalling Chia/Flax Boost dietary supplements because the flaxseed powder contains unapproved herbicide Haloxyfop.

    Product
    care/of Chia/Flax Boost Dietary Supplement; Net Wt. 0.35 oz. (10g) foil packets; Finished Product Item # FCOFBP10G Distributed by Noho Health Inc., New York, NY 10013
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1529-2020·2020-04-01

    Fresenius Medical Care Recalls Honeywell Pressure Transducers for Hemodialysis Systems

    Fresenius Medical Care is recalling 3,561 Honeywell pressure transducers used in hemodialysis delivery systems due to lower long-term reliability.

    Product
    Honeywell Pressure Transducer- Part Number: 370506-22. It is a component used in 2008T, Common Name: Hemodialysis Delivery System; 2008T HD SYS. BLUE STAR; 2008K2, Common Name: Hemodialysis Delivery Equipment; 2008K@home, Common Name: Hemodialysis Delivery System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0901-2020·2020-04-01

    Organic By Nature Supermeal Vanilla Chai Recalled for Unapproved Herbicide

    Organic By Nature is recalling L.O.V.E. Supermeal Vanilla Chai because it contains Organic Ground Flaxseed powder contaminated with the unapproved herbicide Haloxyfop.

    Product
    L.O.V.E. Supermeal Vanilla Chai: 1320g Plastic Bottle, 660g Bio Bag Terra Pouch; Finished Product Item #: 2910E, 2910, 2910-P65, 2911, 2911-P65 Platinum Health Europe, Netherlands, Purim Health Products, Rancho Dominguez, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1539-2020·2020-04-01

    Siemens ADVIA Chemistry Total Bilirubin Assay Recalled for Positive Bias

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Total Bilirubin assays because they may show falsely high results for patients taking eltrombopag.

    Product
    ADVIA Chemistry Total Bilirubin_2 assay- SMN: 10341115 (40 mL) & 10341113 (70 mL). Product Usage: ADVIA TBIL_2 is for in vitro diagnostic use in the quantitative determination of total bilirubin in human serum and plasma of adults and neonates on the ADVIA¿ Chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1578-2020·2020-04-01

    Bard X-Port isp MRI Implantable Port Recall for Incorrect Tunneler Tip

    Bard Peripheral Vascular Inc is recalling 225 X-Port isp MRI Implantable Ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.

    Product
    1. X-Port isp M.R.I Implantable Port, with Pre-Attached 9.6 F Open-Ended Single-Lumen Venous Catheter, REF:0607550, UDI:(01)00801741026195 2. X-Port isp M.R.I. Implantable Port, with Attachable 9.6F Open-Ended Single-Lumen Venous Catheter, REF: 0657525, UDI:(01)00801741026379…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1060-2020·2020-04-01

    Nystatin Oral Suspension Recalled for Low Potency

    Pharmaceutical Associates, Inc. is recalling Nystatin Oral Suspension because it tested below the required potency level.

    Product
    NYSTATIN — NYSTATIN (NYSTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0897-2020·2020-04-01

    Nested Naturals Super Kids Powder Recalled for Unapproved Herbicide

    Organic By Nature, Inc. is recalling Nested Naturals Super Kids powder because the flaxseed ingredient contains an unapproved herbicide.

    Product
    Nested Naturals Super Kids; Superfood Powder Full of Nutrients for Growing Bodies; Whole Food Powder, Net Wt. 7.5 oz (210g), 30 servings; Finished Product Item # FNNKFMSG210G; Bulk Finished Product Item # FGBPNNKFMSG Distributed by Nested Naturals Vancouver, BC, Canada
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1547-2020·2020-04-01

    Randox Chemistry QC Premium Plus Recalled for Incorrect Sodium Values

    Randox Laboratories is recalling Chemistry QC Premium Plus due to incorrect Sodium target values. The error affects quality control accuracy for diagnostic assays.

    Product
    Chemistry QC Premium Plus, Cat. No. LAL4213, GTIN 05055273209006 - Product Usage: This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The device is for the control of accuracy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0894-2020·2020-04-01

    Alkamind Creamy Vanilla Organic Daily Protein Recalled for Unapproved Herbicide

    Organic By Nature, Inc. is recalling Alkamind Creamy Vanilla Organic Daily Protein because the flaxseed powder ingredient contains unapproved herbicide Haloxyfop.

    Product
    Alkamind Creamy Vanilla Organic Daily Protein; 450g Plastic Bottle; Finished Product Item # FAMVDP450G; 3 core alkaline proteins Distributed by Alkamind LLC, New York, NY 10028
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1541-2020·2020-04-01

    Siemens Dimension Vista Total Bilirubin Reagent Cartridge Recall

    Siemens Healthcare Diagnostics is recalling Dimension Vista Total Bilirubin reagent cartridges because they may produce inaccurate results for patients taking eltrombopag.

    Product
    Dimension Vista¿ Total Bilirubin Flex¿ reagent cartridge -In vitro Diagnostic for the determination of total bilirubin. SMN: 10445146 Product Usage: Dimension Vista TBIL method is an in vitro diagnostic test intended to quantitatively measure total bilirubin in human…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0896-2020·2020-04-01

    Organic By Nature Slim Natural Raw Meal Recalled for Unapproved Herbicide

    Organic By Nature is recalling Slim Natural Raw Meal due to the presence of unapproved herbicide Haloxyfop in the flaxseed powder.

    Product
    Erom, Inc. Slim Natural Raw Meal; Bulk; Finished product item # FGBPEIOS-E
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1599-2020·2020-04-01

    Siemens Atellica CH Ethyl Alcohol Assay Recalled for Calibration Bias

    Siemens Healthcare Diagnostics is recalling Atellica CH Ethyl Alcohol assays due to potential positive bias in results within the 10-day calibration interval.

    Product
    Atellica CH Ethyl Alcohol, Test Code ETOH, Siemens Material Number (SMN) 11097501, UDI 00630414596112. The product is an ethyl alcohol assay, IVD use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0902-2020·2020-04-01

    Organic By Nature Recalls RAWr! Life Superfoods Due to Unapproved Herbicide

    Organic By Nature is recalling RAWr! Life Organic Superfoods because the flaxseed powder ingredient contains an unapproved herbicide.

    Product
    RAWr! Life Organic Superfoods; Dietary Supplement; 300g Plastic Bottle (10.60 oz.); Finished Product Item # FHEEG300G Rawr! Life, Glendale, AZ 85308
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0893-2020·2020-04-01

    Alkamind Creamy Chocolate Protein Recalled for Unapproved Herbicide

    Organic By Nature, Inc. is recalling Alkamind Creamy Chocolate Organic Daily Protein due to the presence of unapproved herbicide Haloxyfop in the flaxseed powder ingredient.

    Product
    Alkamind Creamy Chocolate Organic Daily Protein; 450g Plastic Bottle; Finished Product Item # FAMCDP450G; 3 core alkaline proteins Distributed by Alkamind LLC, New York, NY 10028
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1570-2020·2020-04-01

    Bard PowerPort Implantable Ports Recalled Due to Incorrect Catheter Barb Tip

    Bard Peripheral Vascular Inc is recalling 178 PowerPort implantable ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgery.

    Product
    1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard, With suture Plugs, (01)00801741026720; 2. PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single- Lumen Venous Catheter, REF: 1709601, Air Guard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0899-2020·2020-04-01

    Purim Daily Fiber Blend Recalled for Unapproved Herbicide Contamination

    Organic By Nature, Inc. is recalling Purim Daily Fiber Blend because the flaxseed ingredient contains unapproved herbicide Haloxyfop.

    Product
    Purim Daily Fiber Blend - Original unflavored; 540g Plastic Bottle, 180g Plastic Bottle; Finished Product Item#: 2014, 2014-P65, 2015, 2015-P65 Purim - Rancho Dominguez, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1049-2020·2020-04-01

    FDA Recalls Colostat Homeopathic Remedy Due to Incorrect Labeling

    Grato Holdings, Inc. is recalling 659 bottles of Colostat homeopathic remedy because the indications on the product label are incorrect.

    Product
    COLOSTAT — COLOSTAT (RHAMNUS PURSHIANA, SPIGELIA ANTHELMIA, TARAXACUM OFFICINALE, CAJUPUTUM, HYDRASTIS CANADENSIS, ALUMINA, CINA, CINCHONA OFFICINALIS, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, MANDRAGORA OFFICINARUM, NUX VOMICA)
    Category
    Drug
    Distribution
    Distributed nationwide