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.

6826–6850 of 72996

  • SevereNHTSA·25V257000·2025-04-17

    Volvo truck idler gear can detach from the engine causing stall

    Volvo Trucks is recalling certain 2022-2025 VN and 2025 New VN trucks because improperly tightened idler gear bracket fasteners may allow the idler gear to detach from the engine.

    Product
    VOLVO — VOLVO VNL (4), VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V250000·2025-04-17

    Altec Recalls 2014-2016 AT200A Aerial Devices Due to Frame Cracks

    Altec is recalling 2014-2016 AT200A aerial devices because cracks in the mounting frame legs may cause the side plate to break, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V254000·2025-04-17

    Mercedes G-Class may show wrong warning light during stability system failure

    Mercedes-Benz is recalling certain 2025 G 550, G 580 and AMG G 63 vehicles because the electronic stability program may display an incorrect warning light during an ESP system failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 550, AMG G63, G 580 EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V251000·2025-04-17

    Altec Recalls 2024-2025 Digger Derrick Vehicles for Hydraulic Defect

    Altec is recalling 2024-2025 Digger Derrick vehicles because an improperly seated retaining ring may cause hydraulic pressure loss and unintended boom movement.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V258000·2025-04-17

    Autocar Recalls 2023-2024 Xspotter Vehicles Due to Wiring Fire Risk

    Autocar is recalling 2023-2024 Xspotter vehicles because a misrouted alternator ground cable may contact the positive stud, causing damage and increasing the risk of a fire.

    Product
    AUTOCAR — AUTOCAR XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V189000·2025-04-17

    Temsa Recalls 2024-2025 TS45 Buses Due to Incorrect Weight Rating Label

    Temsa is recalling 2024-2025 TS45 transit buses because the Gross Vehicle Weight Rating on the certification label is incorrect, which may lead to unintentional overloading.

    Product
    TEMSA — TEMSA TS45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25227·2025-04-17

    Casely Wireless Portable Power Banks Recalled for Fire and Burn Hazards

    Casely Inc. is recalling Casely Power Pods wireless portable power banks because the lithium-ion battery can overheat and catch fire. The firm has received 51 reports of battery overheating or fire and 6 minor burn injuries.

    Product
    Casely Wireless Portable Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25230·2025-04-17

    Joydeco Roller Window Shades Recalled for Strangulation and Entanglement Hazards

    About 73,000 Joydeco Roller Window Shades sold on Amazon.com have long operating cords that pose strangulation and entanglement hazards to children. The shades violate federal window-covering regulations.

    Product
    Joydeco Roller Window Shades
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25231·2025-04-17

    Tip-Over Restraint Kits for Clothing Storage Units Recalled for Tip-Over Hazard

    American Bolt and Screw recalls tip-over restraint kits distributed with clothing storage units made by Canyon Furniture. The plastic zip ties can become brittle and break, allowing furniture to detach and tip over, posing a risk of serious injury or death to children.

    Product
    Tip-Over Restraint Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·25226·2025-04-17

    The North Face Women's Shellista V Mid Waterproof Boots Fall Hazard

    The North Face Women's Shellista V Mid Waterproof Boots are being recalled because the hook on one boot can catch the laces of the other boot, creating a fall hazard. The company has received 28 reports of the hook catching laces, including 15 reports of minor injuries.

    Product
    The North Face Women's Shellista V Mid Waterproof Boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V188000·2025-04-17

    Nissan Kicks certification labels may show incorrect weight and wheel ratings

    Nissan is recalling certain 2025 Kicks vehicles because the certification label may show incorrect Gross Vehicle and Axle Weight Ratings, and some SR trims may state an incorrect wheel size.

    Product
    NISSAN — NISSAN KICKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V247000·2025-04-16

    BMW X3 front brake discs may have been damaged before installation

    BMW is recalling certain 2025 X3 30 xDrive vehicles because the front brake discs may have been damaged during transport before they were installed on the vehicle.

    Product
    BMW — BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0358-2025·2025-04-16

    Haloperidol Decanoate Injection Recalled Due to Sterility Concerns

    Somerset Therapeutics is recalling Haloperidol Decanoate Injection (100 mg/mL, 1 mL vials) due to lack of assurance of sterility caused by bacterial contamination detected in media fill testing.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0355-2025·2025-04-16

    Haloperidol Decanoate Injection Recalled for Sterility Assurance Defect

    Somerset Therapeutics is recalling 997 vials of Haloperidol Decanoate Injection 50mg/mL nationwide due to lack of assurance of sterility following bacterial contamination detected in a media fill validation test.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1543-2025·2025-04-16

    Stimulation RC Clinician Programmer Application Software Communication Issue

    The Stimulation RC Clinician Programmer Application (Model A71400) has a software issue that can permanently disable communication with certain implantable neurostimulators when a specific intraoperative programming sequence is used. Approximately 1,493 devices were distributed worldwide.

    Product
    Stimulation RC Clinician Programmer Application, Model A71400, when used with the Inceptiv (Model 977119) and Intellis Pro (Model 977118) neurostimulators
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0361-2025·2025-04-16

    Chlorpromazine Hydrochloride Tablets Recalled Due to Impurity

    Zydus Pharmaceuticals is recalling chlorpromazine hydrochloride 10 mg tablets due to the presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit. The recall affects 3,144 bottles distributed nationwide.

    Product
    CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V248000·2025-04-16

    Yamaha motorcycle throttle position sensor fault can stall the engine

    Pure Sports Distributing is recalling certain 2021-2025 Yamaha MT-09, MT-10 and XSR900 motorcycles because throttle position sensor brushes may slide excessively, causing unstable idling or an engine stall.

    Product
    YAMAHA — YAMAHA XSR900, MT-09 SP, MT-10, MT-09
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0702-2025·2025-04-16

    365 Whole Foods Market Frozen Macaroni and Cheese Recall

    365 Whole Foods Market Small Bites Macaroni & Cheese (8.5 oz) is being recalled because it contains undeclared eggs and pork, which pose a hazard to consumers with allergies.

    Product
    365 Whole Foods Market Small Bites Macaroni & Cheese. Net Wt 8.5 oz (240g) Keep Frozen. UPC 99482499709. Distributed by: Whole Foods Market, Austin, TX
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0360-2025·2025-04-16

    Proactiv Skin Smoothing Exfoliator recalled for benzene contamination

    Alchemee, LLC is recalling Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%) due to the presence of benzene, a known chemical contaminant.

    Product
    Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%), Packaged as a) 6 fl. oz. (177.4 mL), UPC 7 35786 01528 2; b) 0.33 OZ (9.45g), UPC 8 42944 10223 1; Distributed by Alchemee, LLC, Santa Monica, CA 90401,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0354-2025·2025-04-16

    Methocarbamol Injection USP Recalled Due to Sterility Assurance Concerns

    Somerset Therapeutics is recalling Methocarbamol Injection USP (1,000 mg/10 mL vials) nationwide due to lack of assurance of sterility following bacterial contamination in media fill testing.

    Product
    METHOCARBAMOL — METHOCARBAMOL (METHOCARBAMOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0359-2025·2025-04-16

    Proactiv Emergency Blemish Relief recalled for benzene contamination

    Alchemee LLC is recalling Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%) due to the presence of benzene, a chemical contaminant. The recall affects approximately 38,237 bottles distributed nationwide.

    Product
    Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%), 0.33 oz. (9.45 g), Distributed by Alchemee LLC, Santa Monica, CA 90401, Made in the USA, UPC 7 35786 01921 1, UPC 8 42944 10223 1, and also packaged as a twin pack UPC 8 42944 10241 5,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0356-2025·2025-04-16

    Haloperidol Decanoate Injection Recalled for Sterility Assurance Failure

    Somerset Therapeutics is recalling Haloperidol Decanoate Injection 50mg/mL vials nationwide due to lack of assurance of sterility from bacterial contamination detected in media fill testing.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0357-2025·2025-04-16

    Haloperidol Decanoate Injection Recalled for Sterility Assurance Failure

    Somerset Therapeutics is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility resulting from bacterial contamination detected during media fill testing. The recall affects 23,960 vials distributed nationwide.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1530-2025·2025-04-16

    Wayson Hydrocolloid Bandages Recalled Due to Sterility Compromise Risk

    Medline Industries is recalling multiple Wayson Hydrocolloid bandage models due to potential compromise of device sterility. The recalled products were distributed nationwide in the US and internationally.

    Product
    Wayson Hydrocolloid Models: 1) Model Number: CUR5103, DBD-BNDG,WTRPRF,HYDRCLLD,CLR,2.36X3.93", 2) Model Number: MJ18004, DBD-MEIJER,BANDAGE,HYDROCOLLOID,HEEL,OVL 3) Model Number: MJ18005, MEIJER,BANDAGE,HYDROCOLLOID,ALLPURP,10CT 4) Model Number: MJ76126V1, DBD-MEIJER,HYDROCOL
    Category
    Medical Device
    Distribution
    Distributed nationwide