The Recall Desk

State

American Samoa product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27626–27650 of 73601

  • SevereFDA (Drugs)·D-1564-2020·2020-09-16

    Just Hand Sanitizer Recalled for Methanol Labeling Error

    Open Book Extracts is recalling Just Hand Sanitizer because it was labeled to contain methanol.

    Product
    Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count NDC 78065-2020-2 UPC 703123998598 (Single packs NDC 78065-2020-1 UPC 703123998659) Distributed by: Just Hand Sanitizer
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2882-2020·2020-09-16

    CareFusion Recalls BD Alaris Modules for Incorrect Syringe Display

    CareFusion 303, Inc. is recalling BD Alaris Syringe and PCA Modules because they may display incorrect syringe types or sizes, potentially causing infusion errors.

    Product
    BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System; Syringe/PCA Sizer Sensor Replacement Kit, P/N 122278652
    Category
    Medical Device
    Distribution
    54 states
  • SevereFDA (Food)·F-1424-2020·2020-09-16

    Signature Select Granola Bars Recalled for Undeclared Peanut Butter

    Treehouse Foods is recalling Signature Select Chewy Granola Bars because they may contain undeclared peanut butter. The recall covers 1,202 cases distributed nationwide and to Saudi Arabia.

    Product
    Signature Select Chewy Granola Bars, Chocolate Chip, Family Pack, 18 bars, UPC 021130-283637. 18-0.84 oz. Net Wt 15.2 oz (432g) Distributed By Better Living Brands LLC PO Box 99, Pleasanton, CA 94566-0009,
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1565-2020·2020-09-16

    Shine & Clean Hand Sanitizer Recalled for Methanol and Low Ethanol

    Maquiladora Miniara S.A. de C.V. is recalling Shine & Clean Hand Sanitizer gel because FDA testing found undeclared methanol and ethanol levels below the label claim.

    Product
    Shine & Clean Hand Sanitizer gel, (Ethyl Alcohol 70%), 33.81 fl oz (1L) bottle, Made in Mexico By: Maquiladora Miniara S.A. de C.V. Carrerera Teoloyucan Huehuetoca km: 22 S/N La Planada Mexico C.P.: 54665 NDC 76753-001-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1563-2020·2020-09-16

    Open Book Extracts Recalls Hand Sanitizer Labeled With Methanol

    Open Book Extracts is recalling Always Be Clean Hand Sanitizer because it is labeled to contain methanol. The recall covers 340,000 packs distributed nationwide.

    Product
    Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ (1.2 mL) packaged in a) Single snaps (NDC 75091-2020-1 UPC 375091202016); b) 100-count boxes (NDC 75091-2020-2 UPC 375091202023); c) 25-count boxes (NDC 75091-2020-3 UPC 375091202030)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2938-2020·2020-09-16

    Qiagen SARS-CoV-2 Test Panel Recalled for Influenza A False Positives

    Qiagen is recalling 1,474 QIAstat-Dx Respiratory SARS-CoV-2 Panel kits due to an increased rate of false positive results for Influenza A, which may lead to inappropriate antiviral use or delayed diagnosis.

    Product
    QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative detection and differentiation of nucleic acid from multiple respiratory viral and bacterial organisms, including the SARS-CoV-2 virus, in nasopharyngeal swabs…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20183·2020-09-16

    RH Recalls Industrial Three-Panel Mirrors Due to Injury Hazard

    RH is recalling about 270 Industrial Three-Panel Mirrors because the panels can detach and fall, posing an injury hazard. No injuries have been reported.

    Product
    Industrial Three-Panel Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V560000·2020-09-16

    2020-2021 Kia Stinger fuel pump defect causing engine power loss

    Kia is recalling 2020-2021 Stinger vehicles because a fuel pump defect may block fuel flow to the engine, causing loss of power while driving and increasing crash risk.

    Product
    KIA — KIA STINGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V561000·2020-09-16

    Volkswagen Recalls 23 Internal Use Vehicles for Regulatory Compliance Issues

    Volkswagen is recalling 23 internal use vehicles, including Golf and Passat models, because they may not meet federal safety standards. Owners will be offered a repurchase.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF ALLTRACK, EGOLF, PASSAT, GOLF R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20184·2020-09-16

    Monoprice Recalls Category 6 Ethernet Cables Due to Fire Hazard

    Monoprice is recalling Category 6 Ethernet cables that do not meet flammability standards, posing a fire hazard. Consumers should stop using the cables and contact the company for a free replacement.

    Product
    Monoprice Category 6 Ethernet Bulk CMR Communications Cables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1432-2020·2020-09-16

    Kader Exports Recalls Frozen Cooked Shrimp Due to Salmonella Risk

    Kader Exports is recalling 406,080 lbs of frozen cooked shrimp from multiple brands due to possible Salmonella contamination. The product was distributed nationwide.

    Product
    Cooked, Peeled and Deveined, Tail-on, Shrimp. AQUA STAR RESERVE-(1) 26/30 shrimp per pound, NET WT 1lbs UPC:3114960591 and (2) 31/40 shrimp per pound, NET WT 1lbs UPC:3114965212. CENSEA- (1) 31/40 shrimp per pound, NET WT 32Oz, 2lbs, 908g UPC:7004160011,(2) 41/50 shrimp…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0013-2021·2020-09-16

    Teva Recalls Cephalexin Oral Suspension Due to CGMP Deviations

    Teva Pharmaceuticals is recalling Cephalexin for Oral Suspension because current Good Manufacturing Practice deviations may cause active ingredient levels to fall outside specification limits.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0012-2021·2020-09-16

    Teva Recalls Cephalexin Oral Suspension Due to CGMP Deviations

    Teva Pharmaceuticals is recalling specific lots of Cephalexin for Oral Suspension because current Good Manufacturing Practice deviations may cause active ingredient levels to fall outside specification limits.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2943-2020·2020-09-16

    Talladium Luminesse Zirconia Discs Recalled for Incorrect Shrinkage Labeling

    Talladium Inc is recalling 39 Luminesse Zirconia Discs because the linear shrinkage value on the label is incorrect and outside the acceptable range.

    Product
    Talladium Luminesse Zirconia Discs, Zirconia HT Disc 98x20mm A1, Shaded Zirconia Blend 2.0 50# A1, Model No. 5147-A1;(UDI): D7915147A10 - Product Usage: are intended for CAD/CAM fabrication of all-ceramic (no metal) dental restorations. Luminesse ZR Blanks are partially sintered…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2937-2020·2020-09-16

    Hager & Meisinger Recalls Dental Burs Due to Labeling Discrepancy

    Hager & Meisinger is recalling 144 units of SINGLES Carbide dental burs because the US dates on the package label do not match the bar code display.

    Product
    SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage: Cutting of hard structures in the mouth, such as teeth or bone, it is also intended to cut hard metals, plastics, porcelains, and similar materials intended for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1566-2020·2020-09-16

    Teva Recalls Cephalexin Oral Suspension Due to Low Potency

    Teva Pharmaceuticals is recalling Cephalexin for Oral Suspension because test results showed the drug was below the required potency specification.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2948-2020·2020-09-16

    MicroPort Recalls PROFEMUR Modular Necks for Package Insert Update

    MicroPort Orthopedics is voluntarily recalling PROFEMUR Titanium and Cobalt Chrome modular necks to replace older package inserts with the most recent revision.

    Product
    PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2 PHAC1202 PROFEMUR NECK NEUTRAL SHORT COBALT CHROME PHAC1204 PROFEMUR NECK NEUTRAL LONG COBALT CHROME PHAC1212 PROFEMUR NECK A/R VAR/VAL 2 SHORT COBALT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V559000·2020-09-15

    Thor Motor Coach Motorhomes Tire Valve Stem Defect Recall

    Thor Motor Coach is recalling certain 2018-2021 motorhomes because the tire valve stem extension may contact the rim and become damaged, potentially causing tire pressure loss and crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY, VENETIAN, ARIA, PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V554000·2020-09-11

    Isuzu and Chevrolet Recall 2018-2021 Trucks for Starter Cable Fire Risk

    Isuzu and Chevrolet are recalling 2018-2021 FTR and 6500XD trucks because a broken starter ground cable could cause a fire. Owners should contact dealers for a free repair.

    Product
    ISUZU — ISUZU, CHEVROLET FTR, 6500XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E070000·2020-09-11

    Oshkosh Recalls Bendix Pressure Switches for Brake System Air Leak Risk

    Oshkosh is recalling Bendix Pressure Switches sold as aftermarket parts because plastic threads may strip, causing air leaks that can reduce braking performance or disable brake lights.

    Product
    SERVICE BRAKES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V553000·2020-09-11

    Forest River Recalls Vengeance Trailers Due to Incorrect Placard

    Forest River is recalling 2014-2016 Vengeance trailers because the Federal Placard may list an incorrect water capacity, risking overload.

    Product
    FOREST RIVER — FOREST RIVER VENGEANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide