The Recall Desk

State

American Samoa product recalls

73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27026–27050 of 73595

  • HighFDA (Devices)·Z-0283-2021·2020-11-04

    Intuitive Surgical Recalls da Vinci Xi Endoscope Controller for Calibration Error

    Intuitive Surgical is recalling one da Vinci Xi Endoscope Controller because improper calibration may cause the endoscope tip to reach higher temperatures, potentially leading to thermal tissue injury.

    Product
    da Vinci Surgical System, IS 4000; Endoscope Controller, Model Number: 372601-16 (UDI: 00886874114193) is included in the IS 4000 Vision Cart, Model Number: 381121-31 (UDI 00886874110898) - Product Usage: used with an endoscope, surgical instruments, and accessories to perform…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V679000·2020-11-04

    Thor Motor Coach Recalls 2010-2011 Four Winds Montecito Motorhomes

    Thor Motor Coach is recalling 2010-2011 Four Winds Montecito motorhomes because a transfer switch may fail due to heat, increasing fire risk.

    Product
    FOUR WINDS — FOUR WINDS MONTECITO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0284-2021·2020-11-04

    Philips Recalls Sterilizable Defibrillator Paddles Due to Undetected Failure Mode

    Philips is recalling 8,942 sterilizable defibrillator paddles because standard checks may miss a specific failure mode. An updated test procedure is available to detect the issue.

    Product
    Philips Sterilizable Defibrillator Paddles, Switched Internal Paddles, Model Numbers M4741A, M4742A, M4743A, M4744A - Product Usage: used in pairs to transmit a controlled electrical shock from an external defibrillator directly to the exposed heart muscle of a post-pubescent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V680000·2020-11-04

    Transcraft Recalls Platform Trailers Due to Detaching Wheel Stops

    Transcraft is recalling 2016-2021 Platform trailers because adjustable wheel stops may detach, increasing the risk of crash or injury.

    Product
    TRANSCRAFT — TRANSCRAFT PLATFORM TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21020·2020-11-04

    YETI Rambler Travel Mugs Recalled Due to Lid Ejection and Burn Hazards

    YETI is recalling Rambler 20 oz Travel Mugs with Stronghold Lids because the magnetic slider can eject, causing hot liquid to spill and posing burn risks.

    Product
    Rambler® 20 oz Travel Mugs with Stronghold Lids
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0053-2021·2020-11-04

    Boehringer Ingelheim Recalls Catapres Tablets Due to Dissolution Testing Anomaly

    Boehringer Ingelheim is recalling specific lots of Catapres tablets because an extraneous peak was observed during dissolution testing.

    Product
    Catapres (clonidine hydrochloride, USP) 0.3 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, Made in Germany, NDC, 0597-0011-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0052-2021·2020-11-04

    Boehringer Ingelheim Recalls Catapres Tablets Due to Dissolution Testing Anomaly

    Boehringer Ingelheim is recalling specific Catapres tablets because an extraneous peak was observed during dissolution testing. The recall covers products distributed nationwide and in Puerto Rico.

    Product
    Catapres (clonidine hydrochloride, USP) 0.2 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, Made in Germany, NDC, 0597-0007-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0307-2021·2020-11-04

    Exactech Recalls Equinoxe Platform Fracture Stem Due to Incorrect Laser Marking

    Exactech is recalling 25 Equinoxe Platform Fracture Stems because they may be incorrectly laser marked as right stems instead of left stems.

    Product
    Equinoxe Platform Fracture Stem, 6.5mm, Left - Product Usage: The Equinoxe Platform Fracture Stem is indicated for cemented use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0298-2021·2020-11-04

    Siemens Artis one Fluoroscopic X-Ray Systems Recalled for Monitor Malfunction

    Siemens Medical Solutions is recalling 22 Artis one systems because the examination room monitor may become intermittently dysfunctional, causing display issues.

    Product
    Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray System Model: 10848600 - Product Usage: he examination table as an integrated part of the system can be used for X-ray imaging, surgery and interventions. The Artis one can also support the acquisition…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0051-2021·2020-11-04

    Boehringer Ingelheim Recalls Catapres Tablets Due to Dissolution Testing Anomaly

    Boehringer Ingelheim is recalling Catapres tablets because an extraneous peak was observed during dissolution testing. The affected lots were distributed nationwide and in Puerto Rico.

    Product
    Catapres (clonidine hydrochloride, USP) 0.1 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, Made in Germany, NDC, 0597-0006-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0287-2021·2020-11-04

    Boston Scientific Recalls Visual-ICE MRI Cryoablation System Mobile Connection Panel

    Boston Scientific is recalling one unit of the Visual-ICE MRI Cryoablation System Mobile Connection Panel due to an incorrectly installed base.

    Product
    Visual-ICE MRI Cryoablation System Mobile Connection Panel (Visual-ICE MRI MCP) - Product Usage: The system is computer-controlled with a touch screen user interface that allows the user to control and monitor the procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0308-2021·2020-11-04

    Exactech Recalls Equinoxe Platform Fracture Stem Due to Incorrect Laser Marking

    Exactech is recalling 12 Equinoxe Platform Fracture Stems because they may be incorrectly laser marked as right stems when they are left stems.

    Product
    Equinoxe Platform Fracture Stem, 6.5mm, Right - Product Usage: The Equinoxe Platform Fracture Stem is indicated for cemented use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0300-2021·2020-11-04

    RTI Surgical Recalls Streamline TL Navigation System Taps Due to Binding

    RTI Surgical is recalling 420 units of Streamline TL Navigation System taps because they have experienced binding with other devices.

    Product
    Streamline TL Navigation System, Catalog Nos. 02-C-TAP-55-MDN 02-C-TAP-60-L-MDN 02-C-TAP-65-L-MDN 02-C-TAP-65-MDN 02-C-TAP-75-L-MDN 02-C-TAP-85-L-MDN 02-C-TAP-85-MDN 02-C-TAP-95-L-MDN 02-RS-INS-C-MDN 02-RS-INSERTER-MDN 02-SCREWINS-CL-MDN 02-SCREWINS-C-MDN…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0302-2021·2020-11-04

    Jarrow Formulas Recalls N-A-C Capsules Due to Mislabeling

    Jarrow Formulas is recalling 533 units of N-A-C 500 mg capsules because they were mislabeled as a different product.

    Product
    N-A-C (N-Acetyl-L-Cysteine, 500 mg, 100 capsules; Veggie Caps, white HDPE bottle with RED label Product # 107002 UPC: 790011070023
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V672000·2020-10-30

    Mercedes-Benz Recalls 2019 GLA 250 for Loose Engine Fusebox

    Mercedes-Benz is recalling 2019 GLA 250 vehicles because a loose engine compartment fusebox may damage fuses and disrupt critical safety systems, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V671000·2020-10-30

    Mercedes-Benz Recalls GLE Models Due to Middle Seat Belt Buckle Defect

    Mercedes-Benz is recalling certain 2020-2021 GLE models because the middle seat belt buckle may fall into a gap, rendering it inoperable and leaving occupants unrestrained.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450, AMG GLE53, GLE 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V673000·2020-10-30

    2020 Mercedes-Benz AMG E53 front passenger seat adjustment recall

    Mercedes-Benz is recalling certain 2019-2021 vehicles because the front passenger seat may be missing a mechanical adjustment limit stop. The seat could move outside the safe range relative to the airbag, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 350, E63 AMG, AMG E53, E 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V669000·2020-10-29

    Triple E RV Recalls Motorhomes Due to Propane Leak Risk

    Triple E RV is recalling 2019-2021 motorhomes because an incorrect brass connector on the water heater may cause a propane leak, increasing fire risk.

    Product
    TRIPLE E RV — TRIPLE E RV, SERENITY, TRIPLE E WONDER, S24CB, UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V668000·2020-10-29

    GM Recalls Vehicles for Missing Start-Stop Accumulator Bolts

    General Motors is recalling specific 2018-2020 vehicles because missing bolts on the start/stop accumulator may cause transmission leaks, loss of propulsion, or fire.

    Product
    GMC — GMC, CHEVROLET, CADILLAC TERRAIN, CRUZE, EQUINOX, XT4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V666000·2020-10-29

    BMW Recalls M2 and M4 Coupes for Fuel Injector Vibration Risk

    BMW is recalling 2020-2021 M2 and 2020 M4 Coupes because missing fuel injector components may cause vibration, leading to fuel leaks and fire risk.

    Product
    BMW — BMW M2, M4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21017·2020-10-29

    Mueller Austria Onion Chopper Pro Recalled for Laceration Hazard

    Mueller Austria is recalling Onion Chopper Pro units because a locking tab can detach, allowing hands to slide into the blades. The company reported 137 laceration injuries.

    Product
    Mueller Austria Onion Chopper Pro
    Category
    Consumer Product
    Distribution
    Distributed nationwide