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.

28851–28875 of 73621

  • HighFDA (Devices)·Z-2050-2020·2020-05-27

    Cardinal Health Recalls Urine Drug Controls Due to Temperature Abuse

    Cardinal Health is recalling Alere Professional Urine Drug Controls (Lot KN00146) because they were stored outside approved temperature ranges, which may result in patient misdiagnosis.

    Product
    Professional Urine Drug Control, Item code 88010 - Product Usage: The Alere Professional Cup Urine Drug Controls are compatible with all quantitative and qualitative drug detection procedures which are sufficiently sensitive to detect the control constituents.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2048-2020·2020-05-27

    BD BBL Gram Stain Kit Recalled for Potential False-Positive Results

    Becton Dickinson is recalling 1,469 BD BBL Gram Stain Kits because increased artifacts may be mistaken for bacteria, leading to false-positive results.

    Product
    BD BBLTM Gram Stain Kit with Stabilized Iodine-- IVD For the differential staining of bacteria, Catalog Number: 212539 - Product Usage: Gram Stain Kits and Reagents are used to stain microorganisms from cultures or specimens by the differential Gram method.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2054-2020·2020-05-27

    Skeletal Kinetics Recalls Cranio/Sculpt C Bone Void Filler Due to Sterilization Concerns

    Skeletal Kinetics is recalling 125 units of Cranio/Sculpt C bone void filler because one unit may have been mispackaged and not sterilized.

    Product
    Cranio/Sculpt C, 10cc, Bone Void Filler, UDI: 00813845021129 - Product Usage: CRANIO/SCULPT C is a calcium phosphate bone void filler indicated for the repair or filling of neurosurgical burr holes, other cranial bone defects and craniotomy cuts with a surface area no larger…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2044-2020·2020-05-27

    Medline Recalls Silicone Foley Catheters Due to Loose Particulate

    Medline Industries is recalling specific lots of silicone Foley catheters because loose silicone particulate was found on the device shaft.

    Product
    SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml - Product Usage: Medline Silicone Foley catheter is a flexible tubular device that is inserted through the urethra and used to drain urine into a collection device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20E033000·2020-05-27

    Horizon Recalls Tekonsha Prodigy Electronic Brake Control Kits

    Horizon Global is recalling certain Tekonsha Prodigy electronic brake control kits because they do not adequately warn drivers that foot pedal trailer braking is unavailable when hazard signals are active.

    Product
    ELECTRICAL SYSTEM: INTEGRATED TRAILER BRAKE CONTROL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2051-2020·2020-05-27

    Cardinal Health Recalls Strep B Carrot Broth Due to Temperature Abuse

    Cardinal Health is recalling Strep B Carrot Broth One-Step tubes because they were stored outside approved temperature ranges, which may lead to patient misdiagnosis.

    Product
    Strep B Carrot Broth One-Step, 16x100mm Tube, 6ml, Item code Z46BX - Product Usage: Intended to detect Group B Streptococcus (GBS) from anovaginal specimen collected from pregnant women. If pregnant woman is positive for GBS colonization, this will indicate a need for treatment…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V308000·2020-05-27

    Thor Motor Coach Recalls 2020 Motorhomes Due to Manual Error

    Thor Motor Coach is recalling 566 2020 motorhomes because the owner's manual incorrectly describes the automatic parking function, which could lead to vehicle rollaway.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR SIESTA, SYNERGY, GEMINI, DELANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1282-2020·2020-05-27

    West-Ward Recalls Ethacrynic Acid Tablets for Impurity Failures

    West-Ward Columbus Inc is recalling Ethacrynic Acid Tablets USP, 25 mg, because the product failed impurity and degradation specifications.

    Product
    Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC: 0054-0415-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateCPSC·20127·2020-05-27

    Primark Recalls Kitten Heel Court Shoes Due to Chromium Levels

    Primark is recalling Wide Fit Kitten Heel Court Pumps because the leather insoles contain elevated levels of Chromium VI, posing a risk of skin irritation.

    Product
    Wide Fit Kitten Heel Court Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2064-2020·2020-05-27

    Philips HeartStart MRx Processor Board Replacement Kits Recalled for Damaged Bags

    Philips is recalling HeartStart MRx Processor Board PCA Replacement Kits because damaged ESD bags were used for storing components.

    Product
    HeartStart MRx Processor Board PCA Replacement Kits 453563478461, a component of the Philips HeartStart MRx Monitorl/Defibrillator - Product Usage: is intended for use in hospital and prehospital settings by qualified medical personnel trained in the operation of the device and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2045-2020·2020-05-27

    Boston Scientific Recalls AMS 700 Reservoirs Due to Labeling Error

    Boston Scientific is recalling five AMS 700 100 mL Spherical Reservoirs with InhibiZone because they were incorrectly labeled as a different model.

    Product
    AMS 700 100 mL, Spherical Reservoir with InhibiZone, Part No. 72404156 - Product Usage: intended for use in the treatment of chronic, organic, male erectile dysfunction (impotence).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2067-2020·2020-05-27

    DFINE Vertebral Hydraulic Assemblies Recalled for Incorrect Expiration Dates

    Merit Medical Systems is recalling 228 DFINE Vertebral Hydraulic Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.

    Product
    DFINE Vertebral Hydraulic Assemblies: Hydraulic Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 1402 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological fractures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2073-2020·2020-05-27

    Capso Vision Recalls CapsoCam Plus Capsule Endoscopy Systems Due to Labeling Errors

    Capso Vision, Inc. is recalling 44 CapsoCam Plus video capsule systems because incorrect serial number labels may lead to patient misdiagnosis.

    Product
    CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 - Product Usage: The CapsoCam Plus video capsule system is intended for visualization of the small bowel mucosa in adults. It may be used as a tool in the detection of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2068-2020·2020-05-27

    Merit Medical Recalls DFINE Vertebral Assemblies Due to Incorrect Expiration Dates

    Merit Medical Systems is recalling 63 DFINE Vertebral Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.

    Product
    DFINE Vertebral Assemblies: Hydraulic-Master Syringe Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 3427 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1271-2020·2020-05-27

    Mylan Recalls Aloprim Injection Vials Due to Discoloration

    Mylan Institutional LLC is recalling 3,010 vials of Aloprim (allopurinol sodium) for Injection due to out-of-specification appearance and color results.

    Product
    ALOPRIM — ALOPRIM (ALLOPURINOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1272-2020·2020-05-27

    InvaGen Recalls Gabapentin Tablets Due to Impurity Test Failure

    InvaGen Pharmaceuticals is recalling 2,202 bottles of Gabapentin 600 mg tablets because they failed an impurity test during stability testing.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2038-2020·2020-05-27

    Pega Medical Recalls SLIM System Handle Due to Lot Number Mismatch

    Pega Medical Inc. is recalling three units of the SLIM System handle because the lot number on the instrument does not match the packaging label.

    Product
    Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V301000·2020-05-26

    Altec Recalls Aerial Devices With Incorrect Tow Hitch Load Ratings

    Altec is recalling 2014-2020 Aerial Devices with Class 3 towing hitches that may have incorrect load ratings or damage from overloading, increasing crash risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V302000·2020-05-26

    2020-2021 Keystone Cougar travel trailer cooktop fire hazard

    Keystone is recalling 2020-2021 Cougar travel trailers because the cooktop may not be properly sealed from the furnace, causing burner flames to invert and increasing fire risk. Dealers will inspect and seal it free of charge.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V300000·2020-05-23

    AEV TraumaHawk Ambulances Recalled for Rear Brake Line Wear Risk

    Halcore Group is recalling 2019-2020 AEV TraumaHawk ambulances because rear brake lines may wear from contact with suspension parts, risking brake loss.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2020-EXP ·2020-05-22

    Conagra Recalls Frozen Chicken and Turkey Bowls Due to Rock Contamination

    Conagra Brands is recalling approximately 276,872 pounds of frozen Healthy Choice Power Bowls because they may contain small rocks. No illnesses have been reported.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — Conagra Brands, Inc. Recalls Frozen Not-Ready-To-Eat Chicken and Turkey Bowl Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V298000·2020-05-22

    Mercedes-Benz Recalls 2012 C-Class Vehicles for Incorrect Air Bag Replacement

    Mercedes-Benz is recalling 2012 C-Class vehicles where an incorrect front passenger air bag may have been installed during a prior recall, potentially reducing crash protection.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG C63, C250, C300, C350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V297000·2020-05-22

    2020-2021 Forest River Surveyor Travel Trailers Safety Chain Recall

    Forest River is recalling 2020-2021 Surveyor travel trailers because the safety chains are insufficient for the trailer's weight rating and may break if the trailer becomes unhitched, risking complete detachment.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V299000·2020-05-22

    Triple E Recalls 2020 Unity Travel Trailers Due to Latch Defect

    Triple E is recalling 2020 Unity travel trailers because a latch may lock, blocking access to the propane shutoff valve and increasing fire risk.

    Product
    TRIPLE E — TRIPLE E UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide