The Recall Desk

State

American Samoa product recalls

73,495 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 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24301–24325 of 73520

  • HighFDA (Devices)·Z-1988-2021·2021-07-07

    Philips Monitor Bracket Assembly falls due to shaft wear in medical imaging systems

    Philips monitor bracket assemblies for CT/PET imaging systems may detach due to shaft wear, posing a risk of the monitor falling and causing serious injury to patients, operators, or bystanders.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 882446 - Vereos PET/CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1996-2021·2021-07-07

    Infusion Pump Order Form Discontinued Due to Ambiguous Reuse Instructions

    Flowonix Medical is recalling physician order forms for Prometra infusion pumps due to ambiguous wording that could be misinterpreted as instructions to reuse previously extracted medication, posing an infection risk.

    Product
    Physician Order Form (PL-15400-00, Nov. 2018) distributed to end user used with the following: Prometra Programmable Infusion Pump System: MODEL/CATALOG #(s): Catalog No. US Model GTIN-14 11827 Prometra Programmable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21160·2021-07-07

    Sovereign Athletic Children's Robes Recalled for Flammability Hazard

    One Twenty Clothing Company is recalling Sovereign Athletic-branded children's robes that fail to meet federal flammability standards for sleepwear, posing a burn hazard to children.

    Product
    Children's Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0745-2021·2021-07-07

    JUST Egg Plant Egg Bites recalled for undeclared egg and milk

    Cuisine Solutions is recalling JUST Egg Inspired by India Curry, Broccoli, Cauliflower, Coconut Milk, Lemongrass Sous Vide Plant Egg Bites due to undeclared egg and milk allergens. The product was distributed nationwide.

    Product
    JUST Egg Inspired by India Curry, Broccoli, Cauliflower, Coconut Milk, Lemongrass 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402511, Expiration dates 3/5/2022, 3/31/2022, and 4/9/2022.16 cartons per corrugated case, Carton GTIN 7 05044 02511 7 Case Bar Code 10…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V514000·2021-07-07

    Wayfarer Recalls 2017-2021 Recreational Vehicles Due to Valve Stem Defect

    Wayfarer is recalling 2017-2021 recreational vehicles because valve stem extenders may rub against wheel liners, potentially causing sudden tire pressure loss and increasing crash risk.

    Product
    WAYFARER — WAYFARER WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1977-2021·2021-07-07

    Exactech Humeral Augmented Tray orthopedic implant components recalled for disengagement risk

    Exactech is recalling Humeral Augmented Tray (HAT) orthopedic implant components because the retaining ring may disengage during use. The recall affects 36 devices distributed in six U.S. states.

    Product
    Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT. Each tray contains 1 of each of the following catalog numbers for a total of 6 trials/tray: (1) HAT STD Left Tray Trial, Cat. #321-00-01; (2) HAT STD Right Tray Trial, Cat. #321-00-02; (3) HAT LAT Left…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1997-2021·2021-07-07

    Tempus Pro Patient Monitor Software Error Risk When Unplugged

    Remote Diagnostic Technologies is recalling Tempus Pro patient monitors (Trizeps 7 variant) that can produce error states when unplugged while connected to a specified laryngoscope device. No injuries have been reported.

    Product
    Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. Part No. - 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. Product Usage: intended to be used as a stand-alone monitor or as a telemedicine system (transmitting patient data to other medical professionals…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1985-2021·2021-07-07

    Monitor Bracket Assembly Wear May Cause Fall Hazard for Medical Imaging Equipment

    Philips medical imaging equipment monitor bracket assemblies may detach due to unrecognized shaft wear, risking the monitor falling and causing serious injury to patients, operators, or bystanders.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728332 - IQon Spectral CT : IQon Spectral CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1994-2021·2021-07-07

    Bard PowerPICC Catheter Kits Recalled for Wrong Guidewire Size

    Bard Access Systems is recalling PowerPICC catheter convenience kits with incorrect guidewires. Kits labeled as containing 70 cm guidewires actually contain 50 cm guidewires, which could affect proper catheter placement.

    Product
    5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire Unit Label: PowerPICC REF CK000340B BARD MYPICC KIT 5F French Size Dual-Lumen 70cm Guidewire
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2021·2021-07-07

    Philips CT Monitor Bracket Assemblies Recalled for Detachment Risk

    Philips has recalled 1,301 Monitor Bracket Assemblies for CT systems worldwide due to shaft wear that could cause monitors to detach and fall, potentially injuring patients, operators, or service personnel.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728333 - Spectral CT:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1989-2021·2021-07-07

    Philips Medical Monitor Bracket May Detach from Ceiling Mount

    Philips medical imaging monitors with worn bracket assembly shafts may detach from ceiling suspensions and fall on patients, operators, or staff. No injuries have been reported.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 882476 - Gemini TF Big Bore PET/CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0746-2021·2021-07-07

    JUST Egg Plant-Based Bites Recalled for Undeclared Egg and Milk

    Cuisine Solutions is recalling JUST Egg Inspired by Japan Portobello plant-based egg bites because they contain undeclared egg and milk. Consumers with allergies or sensitivities to these allergens should not consume the product.

    Product
    JUST Egg Inspired by Japan Portobello, Mushrooms, Sweet Potatos, Furikake, Soy 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402523, Expiration dates 3/5/2022, 3/31/2022, and 4/9/2022.16 cartons per corrugated case, Carton GTIN 7 05044 02523 0, Case Bar Code 10 750…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1981-2021·2021-07-07

    Monitor bracket assembly recalled for detachment hazard on CT imaging systems

    Philips is recalling 1,301 monitor bracket assemblies for CT/PET-CT imaging systems due to shaft wear that could cause detachment from the suspension arm, potentially resulting in the monitor falling and serious injury.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and PET/CT systems. Brilliance 16 Power, Brilliance 16/10/6 Water/Air 728240/728245/728246 - Brilliance 16 728255/728256/728266 - Brilliance 6 728250/728251…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0743-2021·2021-07-07

    JUST Egg Sous Vide Plant Egg Bites recalled for undeclared egg and milk

    Cuisine Solutions is recalling JUST Egg Inspired by America Roasted Potato, Dill, Chives, Red Bell Pepper, Black Pepper Sous Vide Plant Egg Bites because the product contains undeclared egg and milk allergens that are not listed on the label.

    Product
    JUST Egg Inspired by America Roasted Potato, Dill, Chives, Red Bell Pepper, Black Pepper 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402503, Expiration dates 2/22/2022, 3/1/2022, 3/8/2022, 2/22/2022, and 4/6/2022. 16 cartons per corrugated case, Carton GTIN 7 05044…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1980-2021·2021-07-07

    Philips Continuous CT Fluoroscopy Monitor Bracket Assembly Fall Risk

    Philips is recalling 1,301 Monitor Bracket Assemblies due to shaft wear that could cause the assembly to detach from the ceiling suspension arm. This could result in the monitor falling and causing serious injury to patients, operators, bystanders, or service personnel.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and MX16 Models: 728131
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0643-2021·2021-07-07

    QiYu Hand Sanitizer Recalled for Subpotent Ethyl Alcohol Content

    HoYu (US) Logistics Inc is recalling QiYu Hand Sanitizer (75% ethyl alcohol) because the product is subpotent. The recall affects 30,880 bottles distributed nationwide.

    Product
    QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui Cosmetics Co., Ltd, Baiyun District, Guanzhou, China Distributed by HoYu (US) Logistics Inc UPC 6 926645 716288
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V511000·2021-07-06

    Northwood Recalls 2019 Trailers Due to Potential Gas Leak Risk

    Northwood is recalling specific 2019 Nash and Arctic Fox trailers because a stove component may cause a gas leak, increasing fire risk.

    Product
    NORTHWOOD — NORTHWOOD NASH, ARCTIC FOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E061000·2021-07-06

    Yorkim LED Headlight Bulbs Recalled for Excessive Glare and Brightness

    Guangzhou Yorkim Trading Co., Ltd is recalling Yorkim R7 H11 LED bulbs sold on Amazon because they create excessive glare, failing federal safety standards.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·023-2021·2021-07-03

    Tyson Recalls Ready-to-Eat Chicken Products Due to Listeria Contamination

    Tyson Foods is recalling approximately 8.9 million pounds of ready-to-eat chicken products due to possible Listeria monocytogenes contamination linked to illnesses and one death.

    Product
    Tyson Foods Inc. Recalls Ready-To-Eat Chicken Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V507000·2021-07-02

    Spartan Fire Vehicles Recalled for Fuel Rail Leak Fire Risk

    Marion Body Works is recalling 2017-2020 Spartan Fire MetroStar and Gladiator vehicles because a fuel rail leak could cause a fire.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V506000·2021-07-02

    Newmar recreational vehicles recalled for fuel rail sealing defect

    Newmar recalls 2017-2021 Mountain Aire, New Aire, Ventana, and Dutch Star RVs with Cummins diesel engines for a fuel rail sealing defect that can leak, increasing fire risk. Owners should contact Newmar for free inspection and repair.

    Product
    NEWMAR — NEWMAR NEW AIRE, VENTANA, DUTCH STAR, MOUNTAIN AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V508000·2021-07-02

    2020-2021 Braxton Creek Travel Trailers Recalled for Stove Gas Leak Risk

    Braxton Creek is recalling 2020 and 2021 LX and BX travel trailers with Dometic cooking stoves due to an overtightened saddle valve bolt that can damage the o-ring seal and cause a continuous gas leak, posing a fire risk.

    Product
    BRAXTON CREEK — BRAXTON CREEK LX, BX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V509000·2021-07-02

    Mercedes-Benz Recalls Vehicles for Incorrectly Adjusted LED Headlights

    Mercedes-Benz is recalling specific 2018-2021 models because LED headlights may have been incorrectly adjusted during repair, reducing visibility and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, AMG GLE63, GLE 580, AMG GLE53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V504000·2021-07-01

    GM Recalls 2015-2016 Chevrolet and GMC Trucks for Air Bag Defect

    General Motors is recalling 2015-2016 Chevrolet Silverado and GMC Sierra trucks because the roof-rail air bag inflator may rupture or detach, posing an injury risk.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500, SIERRA 2500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide