The Recall Desk

State

American Samoa product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43351–43375 of 73834

  • HighFDA (Food)·F-2200-2017·2017-05-17

    Pinnacle Foods Recalls Great Value Bread and Butter Chips for Glass Fragments

    Pinnacle Foods is recalling Great Value Bread and Butter Chips because glass fragments were found in the product. The chips were distributed nationwide.

    Product
    Great Value Bread and Butter Chips 24 Fl Oz. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716 UPC 078742145990
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2207-2017·2017-05-17

    Treehouse Foods Recalls Macaroni and Cheese Cups for Salmonella Risk

    Treehouse Foods is recalling specific brands of microwaveable macaroni and cheese cups because they may be contaminated with Salmonella.

    Product
    Macaroni & Cheese microwaveable cups sold under the following brands: 1. Big Win Original Macaroni & Cheese Dinner, UPC 11822-58403. 2. Cheese Club express mac Macaroni Cheese Dinner, UPC 41498-17167, 3. Great Value Macaroni & Cheese Dinner, UPC 78742-08249.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V325000·2017-05-17

    Bison Horse Trailers Recalled for Incorrect Weight Rating Labels

    Bison Coach is recalling 2016-2018 horse trailers due to incorrect Gross Axle Weight Rating labels, which may lead to overloading and increased crash risk.

    Product
    BISON — BISON LAREDO, TRAIL HAND, TRAIL BOSS, SILVERADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17154·2017-05-17

    Cabrinha Recalls Kiteboard Control Systems Due to Injury and Fall Hazards

    Cabrinha is recalling about 2,900 kiteboard control systems because a stainless steel component can break, causing loss of kite control and posing injury and fall hazards.

    Product
    Cabrinha Kiteboard control systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2040-2017·2017-05-17

    Siemens RAPIDPoint 500 Blood Gas Analyzer Recalled for Patient ID Error

    Siemens is recalling 159 RAPIDPoint 500 Blood Gas Analyzers because a blank patient ID field may cause demographic errors.

    Product
    RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total hemoglobin, and hemoglobin derivatives in arterial, venous, and capillary whole blood samples.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2054-2017·2017-05-17

    CooperSurgical lnflatoball Pessary Recalled for Incorrect Latex-Free Labeling

    CooperSurgical is recalling lnflatoball Latex Rubber Pessaries because the secondary packaging incorrectly states the product is latex-free, despite being made of 100% latex.

    Product
    CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary Kit. Product Usage: The lnflatoball Pessary is a single-patient use pessary manufactured from natural latex rubber and is used for treating cystocele and/or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2071-2017·2017-05-17

    Stryker PROFESS Registration Kit Recalled for Expiration Date Issues

    Stryker is recalling 65 PROFESS Registration Kits shipped near or past their expiration dates. The kits are used for intranasal and sinus surgery.

    Product
    Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guidance system to enable intranasal and sinus computer-assisted surgery. The system is comprised of PROFESS Registration Stickers, a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0700-2017·2017-05-17

    Sun Pharmaceutical Recalls Olanzapine Tablets Due to Impurity Failures

    Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 7.5 mg, because they failed impurity specifications. The recall covers 6,138 bottles distributed nationwide and in Puerto Rico.

    Product
    Olanzapine Tablets, 7.5 mg, packaged in a) 30-count bottles (NDC 62756-553-83), b) 100-count bottles (NDC 62756-553-88), and c) 1000-count bottles (NDC 62756-553-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0699-2017·2017-05-17

    Sun Pharmaceutical Recalls Olanzapine Tablets Due to Impurity Failures

    Sun Pharmaceutical Industries is recalling specific lots of Olanzapine Tablets, 2.5 mg, because they failed impurity specifications.

    Product
    Olanzapine Tablets, 2.5 mg, 1000-count bottles, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-551-18.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2069-2017·2017-05-17

    Almore Microfil Composite Instruments Recalled for Incorrect Sterile Labeling

    Almore International Inc. is recalling Microfil Composite Instruments because packaging labels incorrectly display a sterile symbol, although the devices are not sterile.

    Product
    Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box. Microfil Composite Instruments are intended to be sterilized by the dentist prior to each use. It is used for composite restoration development. The thin…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0702-2017·2017-05-17

    Sun Pharmaceutical Recalls Olanzapine Tablets Due to Impurity Failures

    Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 20 mg, because they failed impurity specifications. The recall covers 14,784 bottles distributed nationwide and in Puerto Rico.

    Product
    Olanzapine Tablets, 20 mg, packaged in a) 30-count bottles (NDC 62756-556-83), b) 100-count bottles (NDC 62756-556-88), and c) 1000-count bottles (NDC 62756-556-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0703-2017·2017-05-17

    Teva Recalls Prednisolone Oral Solution for Failed Stability Specifications

    Teva Pharmaceuticals USA is recalling specific lots of Prednisolone Oral Solution because they failed stability specifications.

    Product
    PrednisoLONE Oral Solution USP, 15 mg/5mL, alcohol content: 5%(v/v) 240 mL bottle, Rx Only, Manufactured in Canada By: CONTRACT PHARMACEUTICALS LIMITED CANADA, Ontario, Canada, L5N 6L6, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC 0093-6118-87
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0697-2017·2017-05-17

    Akorn Recalls IC-Green Injection Kits Due to Low pH Value

    Akorn, Inc. is recalling 1,292 kits of IC-Green (indocyanine green for injection) due to low pH values. The product was distributed nationwide.

    Product
    IC-Green (indocyanine green for injection, USP), 25 mg, packaged in a kit containing six vials of 25 mg lyophilized powder, Rx only, Manufactured by: Akorn, Inc., NDC 17478-701-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0701-2017·2017-05-17

    Sun Pharmaceutical Recalls Olanzapine Tablets Due to Impurity Failures

    Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 10 mg, because they failed impurity specifications. The recall covers 38,316 bottles distributed nationwide and in Puerto Rico.

    Product
    Olanzapine Tablets, 10 mg, packaged in a) 30-count bottles (NDC 62756-554-83), b) 100-count bottles (NDC 62756-554-88), and c) 1000-count bottles (NDC 62756-554-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V323000·2017-05-16

    Nova Bus Recalls 2016 LFS Artic Buses for Throttle Control Defect

    Nova Bus is recalling 2016 LFS Artic transit buses because a network communication loss may cause the computer to apply full throttle without driver input.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V322000·2017-05-16

    Kenworth T800 and T880 Trucks Recalled for Brake Airline Defect

    PACCAR is recalling 2012-2018 Kenworth T800 and T880 trucks because an incorrectly sized brake control airline may increase stopping distance and crash risk.

    Product
    KENWORTH — KENWORTH T880, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17152·2017-05-15

    VanMoof Recalls B and S Series Bicycles Due to Fender Bolt Hazard

    VanMoof is recalling B and S series bicycles because front fender bolts may not break during obstructions, posing fall and impact hazards.

    Product
    VanMoof B and S series bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E026000·2017-05-15

    Hickory Springs Recalls Summit Seat Covers for Air Bag Deployment Risk

    Hickory Springs is recalling Summit-brand seat covers for RAM ProMaster, Ford Transit, and Mercedes Sprinter vehicles because the seam may prevent seat-mounted air bags from deploying.

    Product
    AIR BAGS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V320000·2017-05-15

    Terex Aerial Devices and Digger Derricks Recalled for Electrical Shock Risk

    Terex is recalling 2007-2016 aerial devices and digger derricks because the onboard electrical breaker may fail to trip during a short circuit, increasing the risk of user injury.

    Product
    TEREX — TEREX AERIAL DEVICES, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide