The Recall Desk

State

American Samoa product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28776–28800 of 73621

  • ModerateFDA (Drugs)·D-1277-2020·2020-06-03

    LidoPatch Pain Relief Patches Recalled Due to Missing Manufacturing Records

    Wuhan Bingbing Pharmaceutical is recalling LidoPatch pain relief patches because missing manufacturing records prevent verification that the product remains within specification through its expiration date.

    Product
    LidoPatch (lidocaine HCl 3.6%, menthol 1.25%) Pain Relief Patch, packaged in 1 patch/box (NDC 10882-527-01); 30 patches/box (NDC 10882-527-02 and 10882-527-04), Manufactured for: JAR Laboratories, Elmhurst, IL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0959-2020·2020-06-03

    Siete Grain Free Cashew Flour Tortillas Recalled for Foreign Material

    Garza Food Ventures is recalling Siete Grain Free Cashew Flour Tortillas due to a potential to contain foreign material.

    Product
    Siete Grain Free Cashew Flour Tortillas NET WT 7 OZ (200g) 8 Count UPC 865336000045 packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1279-2020·2020-06-03

    Mencaine Lidocaine Patches Recalled Due to Missing Manufacturing Records

    Wuhan Bingbing Pharmaceutical is recalling Mencaine patches because manufacturing records and samples were lost, preventing verification that the product remains within specification through expiration.

    Product
    Mencaine (lidocaine 4.5%, menthol 5%) Patch, 1 patch per pouch, Manufactured For: Terrain Pharmaceuticals, Reno, NV 89501; NDC 53225-1090-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0962-2020·2020-06-03

    Jindilli Beverages Recalls Milkadamia Unsalted Buttery Spread for Potential Mold

    Jindilli Beverages LLC is recalling Milkadamia Unsalted Buttery Spread due to the potential to contain mold. The product was distributed nationwide.

    Product
    Milkadamia Unsalted Buttery Spread 8 ounces packaged in plastic tub, 6 packaged per case UPC 858045004725
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2111-2020·2020-06-03

    GE Healthcare Recalls Giraffe Shuttle Upgrade Kits Due to Battery Odor

    GE Healthcare is recalling Giraffe Shuttle upgrade kits because the batteries emit a strong sulfur odor during charging.

    Product
    Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0963-2020·2020-06-03

    Jindilli Beverages Recalls Milkadamia Salted Buttery Spread for Potential Mold

    Jindilli Beverages LLC is recalling 2,981 cases of Milkadamia Salted Buttery Spread due to the potential presence of mold.

    Product
    Milkadamia Salted Buttery Spread 8 ounces packaged in plastic tub, 6 packaged per case UPC 858045004718
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1280-2020·2020-06-03

    CVS Lidocaine Cold and Hot Patch Recalled for Manufacturing Record Loss

    CVS Pharmacy is recalling Maximum Strength Lidocaine Cold & Hot Patches because manufacturing records and samples were lost, meaning the product may not remain within specification through its expiration date.

    Product
    Maximum Strength Lidocaine Cold & Hot Patch (lidocaine 4%, menthol 1%), 5 patches per box, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895; NDC 66902-218-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1274-2020·2020-06-03

    West-Ward Recalls Doxycycline Hyclate Tablets Due to Dissolution Failure

    West-Ward Columbus Inc. is recalling Doxycycline Hyclate 100 mg tablets because they failed a dissolution test at the end of their shelf life.

    Product
    DOXYCYCLINE HYCLATE — DOXYCYCLINE HYCLATE (DOXYCYCLINE HYCLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2140-2020·2020-06-03

    Inpeco FlexLab Automation System Recalled for Sample Association Errors

    Inpeco S.A. is recalling 37 FlexLab Automation Systems due to a firmware communication error that can cause sample tubes to be incorrectly associated with carriers.

    Product
    FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-10), or StaRRsed Interface Module (P/N FLX-268-00)is a modular system designed to automate Pre-Analytical and Post-Analytical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V320000·2020-06-01

    Keystone Recalls 2020 Springdale Trailers Due to Incorrect Axles and Tires

    Keystone RV Company is recalling 2020 Springdale trailers because they were equipped with incorrect axles and tires, which may cause the trailer to be overloaded and increase the risk of a crash.

    Product
    KEYSTONE — KEYSTONE SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V317000·2020-05-29

    Forest River Recalls 2020-2021 Cargo Trailers Due to Safety Chain Defect

    Forest River is recalling 2020-2021 US Cargo, Haulin', and Trail & Sport cargo trailers because safety chains may break if the trailer becomes unhitched.

    Product
    US CARGO — US CARGO, HAULIN' CARGO TRAILER, TRAIL & SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V316000·2020-05-29

    Braun Ambulances Recall 2019 Models Due to Rear Brake Line Wear

    Braun Ambulances is recalling 2019 Chief XL and Liberty ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES CHIEF XL TYPE I, LIBERTY TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V319000·2020-05-29

    GM Recalls 2019-2020 Chevrolet HD Trucks for ABS Warning Light Defect

    General Motors is recalling 2019-2020 Chevrolet 4500HD, 5500HD, and 6500HD trucks because the ABS malfunction light may fail to illuminate, increasing crash risk.

    Product
    INTERNATIONAL MOTORS — INTERNATIONAL MOTORS CHEVY 5500HD, CHEVY 4500HD, CHEVY 6500HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V313000·2020-05-28

    Frazer Recalls 2019-2020 RAM Chassis Emergency Vehicles for Brake Line Wear

    Frazer is recalling 2019-2020 emergency vehicles on RAM 4500 and 5500 chassis because rear brake lines may wear, causing brake failure and increasing crash risk.

    Product
    FRAZER — FRAZER RAM 4500 CHASSIS, RAM 5500 CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V314000·2020-05-28

    Honda and Acura Recall Vehicles for Fuel Pump Failure Risk

    Honda is recalling specific 2018-2020 models because a faulty fuel pump may cause the engine to stall while driving, increasing crash risk.

    Product
    HONDA — HONDA, ACURA ACCORD, INSIGHT, CIVIC, RLX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·011-2020·2020-05-28

    Nestle Recalls Lean Cuisine Fettuccini Alfredo for Undeclared Allergens

    Nestle Prepared Foods is recalling Lean Cuisine Fettuccini Alfredo products because they contain undeclared soy and chicken, which are not listed on the label.

    Product
    Nestle Prepared Foods Company — Nestle Prepared Foods Company Recalls Lean Cuisine Fettuccini Alfredo Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V312000·2020-05-28

    Thor Motor Coach Recalls 2020 Motorhomes for Brake Hose Chafing Risk

    Thor Motor Coach is recalling 566 2020 motorhomes because a fender liner may chafe the brake hose, potentially causing brake fluid loss and increased braking distance.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH CHATEAU CITATION, SIESTA, TIBURON, COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V311000·2020-05-28

    Keystone Recalls 2020 Springdale Trailers Due to Incorrect Tire Labeling

    Keystone RV Company is recalling 2020 Springdale trailers because the Federal Identification Tag lists incorrect tire load range and size, which could lead to tire overinflation or overloading.

    Product
    KEYSTONE — KEYSTONE SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2022-2020·2020-05-27

    K2M Aleutian Lordotic Spreader Recalled Due to Tip Breakage Risk

    K2M, Inc. is recalling Aleutian Lordotic Spreaders because the welded tips may break off during spinal procedures.

    Product
    K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog # 5203-90153, UDI # 10888857108660, Size 28x8mm, 6 Product Usage: Used to simulate the height of the cage and expand the spine disc space to determine the optimal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2017-2020·2020-05-27

    K2M Aleutian Lordotic Spreader Recalled Due to Tip Breakage Risk

    K2M, Inc. is recalling the Aleutian Lordotic Spreader because the welded tip may break off during spinal procedures.

    Product
    K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog # 5203-90135, UDI # 10888857108486, Size 24x4mm, 18 Product Usage: Used to simulate the height of the cage and expand the spine disc space to determine the optimal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2060-2020·2020-05-27

    Bovie Medical Recalls Renuvion J-Plasma Precise Open Handpieces Due to Fracture Risk

    Bovie Medical Corporation is recalling Renuvion/J-Plasma Precise Open Handpieces because unexpected stress fractures may cause the shaft to fragment during clinical use.

    Product
    Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS, BVX-044-BPP, BVX-150-BPP, BVX-150-BPS, APYX-044-BPS, APYX-150-BPP, and APYX-150-BPS - Product Usage: for electrosurgical cutting, coagulation and ablation of soft tissue during open surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide