The Recall Desk

State

American Samoa product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40126–40150 of 73831

  • SevereFDA (Devices)·Z-0350-2018·2018-01-24

    Merge Healthcare Recalls Power Strips in Hemo System Due to Overheating

    Merge Healthcare is recalling 1,150 power strips sold with the Merge Hemo System because an input resistor can overheat and cause the unit to smoke.

    Product
    Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite Power strip (PS-415-HGULTRA - Part Number 13-00106-00) are two components sold as part of the Merge Hemo System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0221-2018·2018-01-24

    Pharmedium Recalls Superpotent Phenylephrine Syringes Nationwide

    Pharmedium Services is voluntarily recalling 2,390 syringes of Phenylephrine HCL 100 mcg/mL due to a superpotent drug classification.

    Product
    Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in 0.9% Sodium Chloride 10 mL syringes, PharMEDium Services, LLC 913 N Davis Ave Cleveland, MS, NDC 71019-263-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0353-2018·2018-01-24

    Zoll LifeVest Wearable Defibrillator Recalled for Defibrillation Shock Failure Risk

    Zoll Manufacturing Corp. is recalling 33,670 LifeVest Wearable Defibrillators due to an incorrect service code that may prevent the device from detecting critical defects, potentially leading to defibrillation shock failure.

    Product
    LifeVest Wearable Defibrillator Model 4000, Product Number 10A0988-A01. The LifeVest system is indicated for patients 18 years of age and older who are at risk for sudden cardiac arrest and are not candidates for or refuse an implantable defibrillator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0378-2018·2018-01-24

    Roche Recalls Automated Analyzers Due to Possible Sample Mismatch

    Roche Diagnostics is recalling 2,517 automated laboratory analyzers due to a software limitation that may cause sample mismatches.

    Product
    Brand Name: ¿ cobas c 6000 MODULAR Series System e 601 ¿ cobas c 8000 MODULAR Series System - e 602 ¿ Roche / Hitachi MODULAR Analytics Combination System Model/Catalog/Part Number: MODULAR Analytics E 170 ¿ 03022109001 ¿ 03023109973 ¿ 03739040001 ¿ 03739040692 ¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18E005000·2018-01-24

    Fuel Helmets Recalling Specific Models Due to Strap Failure Risk

    Fuel Helmets is recalling specific models because the securing strap may fail in extreme temperatures, increasing injury risk in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0598-2018·2018-01-24

    Ventura Foods Recalls Italian Dressing Due to Plastic Foreign Object

    Ventura Foods is recalling single-serve Italian dressing packets because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    Single-serve plastic packet Italian Dressing; Case packing: Sysco Classic Cls Italian 500 12Gm ; 47014SYS; B13017; single-serve plastic packet: Chef's Quality Creamy Italian; Chef's Quality; 60/1.5 OZ Pouches Net Wt 5.6 LB; 16689CHQ, B33317;
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0596-2018·2018-01-24

    Ventura Foods Recalls House Recipe Bleu Cheese Dressing Due to Plastic Foreign Object

    Ventura Foods is recalling 18 cases of House Recipe Bleu Cheese Dressing & Dip because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    plastic cup with foil seal: House Recipe Bleu Cheese Dressing & Dip; Distributed by: Sysco Corporation, Houston, Texas 77077; Net Wt 1.5 OZ.Code: B10127; packed in cardboard case : House Recipe; Distributed By Sysco Corporation; Houston Texas 77077; B10127; HR BluChs…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0382-2018·2018-01-24

    Owen Mumford Recalls Unifine Pentips Pen Needles Due to Sterility Concerns

    Owen Mumford USA is recalling Unifine Pentips pen needles because water exposure may have compromised sterility. Consumers should check for discoloration on the protective seal.

    Product
    Unifine Pentips 5mm x 31G pen needles, packaged in 30 ct pen needles. Product Usage: Sterile, non-toxic, non-pyrogenic, single use pen needles for the subcutaneous injection of drugs from pen injectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0220-2018·2018-01-24

    Pharmedium Recalls Subpotent Ephedrine Sulfate Syringes Nationwide

    Pharmedium Services is recalling 5,002 pre-filled ephedrine sulfate syringes nationwide because the drug was subpotent. The voluntary recall was initiated in October 2017.

    Product
    ePHEDrine Sulfate In 0.9% Sodium Chloride, 5 mg per mL (50 mg per 10 mL), 10 mL Total Volume pre-filled syringes, packaged in a) 5-count cartons, NDC 71030-0003-10 and NDC 71030-0003-20, and b) 25-count cartons, NDC 71030-0003-21 and NDC 71030-0003-12, Rx Only, PharMEDium…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0387-2018·2018-01-24

    Phadia 1000 Instrument Recalled Due to Retry Command Malfunction

    Phadia US Inc is recalling 70 Phadia 1000 Instruments nationwide because a malfunctioning Retry command may cause solution shortages and affect test results.

    Product
    Phadia 1000 Instrument, Article Number 12-3800-01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0595-2018·2018-01-24

    Ventura Foods Recalls A&W Papa Sauce Due to Plastic Foreign Object

    Ventura Foods is recalling A&W Papa Sauce because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    A&W All American Food Papa Sauce; 8/24 OZ. Pouches; Net Wt 12 LB. Paced Exclusively For Use By: A&W and its franchisees., Lexington, KY 40611; Use by: 04 29 18 and 04 30 18;
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·18E006000·2018-01-24

    Dainese Recalls AGV Carbon Modular Helmets Due to Chin Bar Defect

    Dainese is recalling 325 AGV Carbon Modular motorcycle helmets because glue may have caused the chin base material to deteriorate, increasing injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0381-2018·2018-01-24

    Owen Mumford Recalls Unifine Pentips Due to Potential Sterility Compromise

    Owen Mumford USA is recalling Unifine Pentips pen needles because water exposure may have compromised sterility. Users should check for discoloration or yellowing of the protective seal.

    Product
    Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic, non-pyrogenic, single use pen needles for the subcutaneous injection of drugs from pen injectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0228-2018·2018-01-24

    Unichem Recalls Divalproex Sodium Tablets Due to Metronidazole Contamination

    Unichem Pharmaceuticals is recalling Divalproex Sodium tablets because metronidazole powder was found in one bottle. The product was distributed nationwide.

    Product
    DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0592-2018·2018-01-24

    Ventura Foods Recalls Honey Mustard Dressing Due to Plastic Foreign Object

    Ventura Foods is recalling specific lots of honey mustard dressing because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    Gordon Choice Honey Mustard Dressing; Net Contents 128 FL OZ; For Distribution Exclusively For Gordon Food Service, Wyoming, MI 49509 ; Code: 33217.; Honey Mustard Dressing; Keep refrigerated; Net Content 1 Gallon; Ventura Foods, Brea, CA 92821, dtd: 053018; Sysco Reliance…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0594-2018·2018-01-24

    Ventura Foods Recalls Tartar Sauces Due to Plastic Foreign Object

    Ventura Foods is recalling specific lots of Imperial, Classic Gourmet, and Culinary Secrets tartar sauces because a plastic foreign object was introduced into the product stream.

    Product
    Sysco Imperial Tartar Sauce; Net Contents 1 GAL; Distributed by Sysco Corporation, Houston, Texas 77077; Code: 12817; Classic Gourmet Dressings Select Tartar Sauce; Net Contents 1 Gal.; Ventura Foods, Brea, CA 92821; Code 05 30 18; . Culinary Secrets Deluxe Tartar…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0601-2018·2018-01-24

    Ventura Foods Recalls Rio Pacific Deluxe BBQ Sauce Due to Plastic Foreign Object

    Ventura Foods, LLC is recalling Rio Pacific Foods Deluxe BBQ Sauce because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    Rio Pacific Foods Deluxe BBQ Sauce; 3.78 litre; Produced in the USA for Funnybones Foodservice Ltd, Hertfordshire AL7 1HW; Lot #120117
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0214-2018·2018-01-24

    Shiseido Recalls bareMinerals Sunscreen Lotion Due to GMP Deviations

    Shiseido America Inc. is recalling bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion because the manufacturing of active pharmaceutical ingredients did not meet GMP and quality requirements.

    Product
    bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion (zinc oxide 23.8%, titanium dioxide 4.1%), 40 mL/1.35 fl. oz. bottle, Dist. by Bare Escentuals Beauty, Inc. SF, CA 94105 USA, NDC 98132-761-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0597-2018·2018-01-24

    Ventura Foods Recalls House Recipe Ranch Dressing Due to Plastic Foreign Object

    Ventura Foods is recalling 117 cases of House Recipe Ranch Dressing & Dip because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    plastic cup with foil seal: House Recipe Ranch Dressing & Dip; Distributed by: Sysco Corporation, Houston, Texas 77077; Net Wt 1.5 OZ.Code: B10127; packed in cardboard case : House Recipe; Distributed By Sysco Corporation; Houston Texas 77077; B10127; HR Rch 128/1.5 oz…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0590-2018·2018-01-24

    Ventura Foods Recalls French Dressings Due to Plastic Foreign Object

    Ventura Foods, LLC is recalling various French dressings because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    Classic Gourmet Dressing; Country French; Net Wt 1.5 OZ.; Ventura Foods, LLC, Lot codes: 33317; Culinary Secrets Country French Dressing; Net Wt. 1.5 OZ.; Lot Codes: 04 29 18; Sysco Reliance French Style Dressing; Net Contents 1 GAL; Lot codes: B12817; Gordon Choice…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0591-2018·2018-01-24

    Ventura Foods Recalls Gordon Choice Thousand Island Dressing Due to Plastic Contamination

    Ventura Foods is recalling specific lots of Gordon Choice Thousand Island Dressing because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    Gordon Choice Thousand Island Dressing; Net Contents 128 FL OZ; For Distribution Exclusively For Gordon Food Service, Wyoming, MI 49509 ; Code: B33217.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0384-2018·2018-01-24

    Valeant Recalls SPAG-2 Nebulizers for Particle Size Failures

    Valeant Pharmaceuticals is recalling 418 SPAG-2 units and 808 nebulizers because some units failed to meet particle size specifications for ribavirin aerosol administration.

    Product
    Small Particle Aerosol Generator Model SPAG-2 6000 Series (SPAG-2). The SPAG-2 medical device is a pneumatic flow system indicated for the administration of Virazole (ribavirin) aerosol. Driven by a pressurized gas (air or blended oxygen) and uses a nebulizer to generate a fine…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0218-2018·2018-01-24

    Shiseido Future Solutions LX Triple Points Bonus Recalled for GMP Deviations

    Shiseido America Inc. is recalling Shiseido Future Solutions LX Triple Points Bonus because the manufacturing of the active pharmaceutical ingredient did not meet GMP and quality requirements.

    Product
    Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ (octinoxate 4.9%, octocrylebe 3.0%, oxybenzone 1.0% and zinc oxide 15.4%), packaged in 15 mL tubes, Shiseido Americas Corporation Dist. New York, NY 10022, NDC 58411-256-60
    Category
    Drug
    Distribution
    Distributed nationwide