The Recall Desk

State

American Samoa product recalls

72,971 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
5
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 5 (20%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6926–6950 of 72996

  • HighNHTSA·25V230000·2025-04-10

    Coachmen Catalina Travel Trailer Recall for Sewer Gas Risk

    Forest River is recalling 2025 Coachmen Catalina travel trailers because the wastewater pipe may not extend to the exterior, allowing sewer gas to enter the cabin.

    Product
    COACHMEN — COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25219·2025-04-10

    Long-Haul ATV fuel containers recalled for non-child-resistant closure

    Long-Haul 5L ATV fuel containers sold on Amazon.com lack required child-resistant closures, posing burn, fire, and poisoning risks to children. About 815 units sold from January 2023 through October 2024 are recalled.

    Product
    Long-Haul 5L ATV Gas Cans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25221·2025-04-10

    Multifunctional Puzzle Crab Toys with Magnets Recalled for Ingestion Hazard

    About 600 magnetic puzzle crab toys sold on Walmart.com are recalled because swallowed magnets can cause serious digestive injury. Consumers should stop using them immediately and request a full refund.

    Product
    Multifunctional Puzzle Crab Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25215·2025-04-10

    Fisher-Price Brunch & Go Stroller Toys Recalled for Choking Hazard

    Fisher-Price is recalling about 253,000 Brunch & Go Stroller Toys because the egg component can crack and create choking hazards. No injuries have been reported; consumers should immediately stop use and request a free replacement.

    Product
    Brunch & Go Stroller Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25223·2025-04-10

    Safetussin Max Strength Multi-Symptom blister packs recalled for non-child-resistant packaging

    Kramer Laboratories recalls Safetussin Max Strength Multi-Symptom Cough, Cold and Flu blister packs due to packaging that fails to resist child access. Tablets can be pushed through the foil, posing a poisoning risk to young children.

    Product
    Safetussin Max Strength Multi-Symptom Cough, Cold and Flu tablets blister packs
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·25217·2025-04-10

    Modus Furniture Kentfield Dressers Recalled for Tip-Over and Entrapment Hazards

    Kentfield Solid Wood Eight-Drawer Dressers can tip over if not wall-anchored, risking entrapment injuries or death to children. Modus Furniture is offering free repair kits and installation.

    Product
    Kentfield Solid Wood Eight-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25216·2025-04-10

    Fisher-Price Tissue Box Toy in SnugaPuppy Centers Recalled for Choking Hazard

    Fisher-Price is recalling about 15,300 Tissue Box Toys sold with 3-in-1 SnugaPuppy Activity Centers. The toy can detach and expose small brackets that pose a choking hazard to young children.

    Product
    Tissue Box Toy sold with Fisher-Price 3-in-1 SnugaPuppy Activity Centers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V231000·2025-04-10

    2025 Ram 1500 Recalled for Tire Pressure Software Error

    Chrysler is recalling 2025 Ram 1500 vehicles because a software error may display incorrect tire pressure messages, increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V233000·2025-04-10

    Volkswagen ID. Buzz brake warning light may use the wrong symbol

    Volkswagen is recalling certain 2025 ID. Buzz vehicles because the brake system warning light may display the incorrect symbol and colour, failing FMVSS 135 and 101.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID. BUZZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E026000·2025-04-10

    MORryde Recalls Clip-On Brackets Due to Step Detachment Risk

    MORryde is recalling specific Clip-On brackets because mounting bolts may loosen, causing steps to detach and increasing injury risk.

    Product
    STRUCTURE:BODY:STEP/LADDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1495-2025·2025-04-09

    Draeger Anesthesia Circuit Kit Flex 1 recalled for potential hose cracks

    Draeger, Inc. is recalling Anesthesia Circuit Kit Flex 1 devices nationwide and internationally due to potential cracks in the breathing circuit hose that conducts anesthesia gases.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1499-2025·2025-04-09

    Anesthesia Circuit Kit Flex EPA recalled due to breathing hose cracking

    Draeger is recalling the Anesthesia Circuit Kit Flex EPA due to the potential for cracks to form in the breathing circuit hose. Approximately 13,620 units have been distributed domestically and internationally. Users should discontinue use of affected units immediately.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intend
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1493-2025·2025-04-09

    VentStar Flex 220 Breathing Circuit Recalled for Potential Hose Cracks

    Draeger, Inc. is recalling 65,150 units of the VentStar Flex 220 breathing circuit due to the potential for cracks to form in the hose. A crack could affect gas delivery during anesthesia or ventilation procedures.

    Product
    Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients. The breathing circuit is in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1497-2025·2025-04-09

    Anesthesia Circuit Kit Flex 6 Recalled for Potential Breathing Hose Cracks

    Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1496-2025·2025-04-09

    Anesthesia Circuit Kit Flex 2 recalled due to breathing hose crack risk

    Draeger's Anesthesia Circuit Kit Flex 2 is recalled because of the potential for cracks to form in the breathing circuit hose. No injuries have been reported.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1498-2025·2025-04-09

    Anesthesia Circuit Kit Flex (P)2 recalled for potential breathing hose cracks

    Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex (P)2 due to the potential for cracks to form in the breathing circuit hose. This FDA Class I recall affects approximately 9,250 units distributed domestically and internationally.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model/Catalog Number: MP02752 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is inten
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1494-2025·2025-04-09

    Draeger ID Circuit Flex 220 breathing circuit hoses subject to cracking

    Draeger's ID Circuit Flex 220 breathing circuit for anesthesia machines may develop cracks in the hose. The recall affects 3,325 units distributed nationwide and internationally.

    Product
    Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult Component: Not applicable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V216000·2025-04-09

    McLaren brake lines may be routed to the wrong side

    McLaren is recalling certain 2020-2025 vehicles because brake lines may be routed incorrectly, activating the brakes on the wrong side and possibly locking a rear wheel.

    Product
    MCLAREN — MCLAREN ARTURA, 720S SPIDER, GT, 600LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V226000·2025-04-09

    Audi Q6 rearview camera image may be delayed or deactivated

    Volkswagen is recalling certain 2025 Audi Q6 and SQ6 vehicles because the rearview camera image may be delayed or deactivated after shifting into reverse, failing FMVSS 111.

    Product
    AUDI — AUDI SQ6 SPORTBACK E-TRON, Q6 E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25C005000·2025-04-09

    Chicco Recalls MyFit Zip Air Harness and Booster Child Seats

    Chicco is recalling specific MyFit Zip Air Harness and Booster child seats because they may allow excessive chest movement in a crash, increasing injury risk.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1501-2025·2025-04-09

    Phoroptor VRx Digital Refraction System Recalled for Detachable Head

    Reichert is recalling 1,876 units of the Phoroptor VRx Digital Refraction System (Model 16242) due to an assembly defect that could cause the refraction head to detach during eye examinations.

    Product
    Phoroptor VRx Digital Refraction System Model Numbers: 16242
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1473-2025·2025-04-09

    Stryker Nasopore Nasal Dressing Recalled for Compromised Sterility Seals

    Stryker's Nasopore 8cm nasal dressing is being recalled because packaging seals may have bubbles indicating the sterility barrier has been breached. The recall affects 182,344 units distributed nationwide.

    Product
    Nasopore 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Number 5400-020-008ITL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0306-2025·2025-04-09

    Biocon Pharma atorvastatin calcium tablets recalled for failed dissolution specifications

    Biocon Pharma is recalling 2,184 bottles of Atorvastatin Calcium Tablets USP 40 mg nationwide. The product failed to meet required dissolution specifications, which may affect medication absorption.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide