The Recall Desk

State

American Samoa product recalls

73,478 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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23151–23175 of 73503

  • ModerateFDA (Devices)·Z-0018-2022·2021-10-13

    Dental implant scan abutment recalled for dimensional tolerance and marking defects

    Paltop Scan Abutment WP dental implant scanning devices are recalled due to manufacturing defects. Affected units show dimensional tolerance deviations and size marking incongruences that may delay restoration procedures.

    Product
    Scan Abutment WP, Cat. No. 30-70106 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0014-2022·2021-10-13

    Scan Abutment NP Dental Implant Components Recalled for Dimensional Deviations

    Paltop Advanced Dental Solutions is recalling Scan Abutment NP dental implant components due to manufacturing tolerance deviations that may affect implant restoration fit and timing.

    Product
    Scan Abutment NP, Cat. No. 30-70102 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0043-2022·2021-10-13

    ZOLL SOLEX 7 Intravascular Catheter Kit Labeling Update for Potential Leaks

    ZOLL Circulation, Inc. is updating labeling for SOLEX 7 intravascular heat exchange catheter kits to communicate about potential leaks from the catheter or start-up kit tubing. The update affects 5,345 kits with worldwide distribution.

    Product
    ZOLL, REF 8700-0793-40 (SL-2593AE) SOLEX 7, Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens), HEPARIN COATED, Sterile EO, Rx Only, UDI: (00)849111075312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V792000·2021-10-12

    KTM and Husqvarna Recall Motorcycles for Clutch Slave Cylinder Defect

    KTM North America is recalling specific 2018-2020 KTM and Husqvarna motorcycles because a damaged gasket on the clutch slave cylinder may prevent the clutch from disengaging, increasing crash risk.

    Product
    KTM — KTM, HUSQVARNA 690 ENDURO R, 701 ENDURO LR, 690 DUKE, ENDURO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V793000·2021-10-12

    2019-2022 Winnebago Travato and Boldt RV Electrical Fire Hazard

    Winnebago is recalling 2019-2022 Travato and 2021-2022 Boldt RVs. A faulty wire harness may lose over-current protection, causing wires to overheat and increasing fire risk. Owners must not drive until the Volta Power System is disabled.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, BOLDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V789000·2021-10-11

    Mercedes-Benz Recalls 2021 S-Class Models for Air Bag Software Defect

    Mercedes-Benz is recalling 2021 S 500 and S 580 vehicles because a software defect may deactivate the front passenger air bag, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 500, S 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V790000·2021-10-11

    HME Recalls 2017-2020 Fire Trucks Due to Fuel Rail Leak Risk

    HME is recalling 245 fire trucks from 2017-2020 because a sealing washer may not seat correctly, allowing the high-pressure fuel rail to leak and increasing fire risk.

    Product
    HME — HME, HME AHRENS-FOX 1871, COMMFOX, AERIAL, AF1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V788000·2021-10-09

    Foretravel Recalls 2020-2022 RVs Due to Window Adhesive Failure

    Foretravel is recalling 2020-2022 iH-45, Realm, and iC-37 recreational vehicles because window adhesive may fail, causing the vent to detach and increasing crash risk.

    Product
    FORETRAVEL — FORETRAVEL IC-37, IH-45, REALM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V785000·2021-10-08

    Forest River Recalls 2021-2022 Entrada Motorhomes Due to Brake Line Wear

    Forest River is recalling 2021-2022 Entrada motorhomes because brake lines may wear against leveling jack brackets, potentially causing brake failure and increasing crash risk.

    Product
    EAST TO WEST — EAST TO WEST ENTRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V787000·2021-10-08

    Starcraft Transit Bus Recall for Incorrect Emergency Exit Window Labels

    Forest River is recalling 2012-2016 Starcraft transit buses because rear emergency exit window labels are misplaced and incomplete, potentially delaying evacuation.

    Product
    STARCRAFT BUS — STARCRAFT BUS TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V786000·2021-10-08

    Star Trans School Bus Recall for Incorrect Emergency Exit Window Labels

    Forest River is recalling 2014-2016 Star Trans school buses because rear emergency exit window labels are misplaced and incomplete, potentially delaying evacuation.

    Product
    STARTRANS — STARTRANS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·037-2021·2021-10-08

    Crider Foods Recalls Canned Beef With Gravy Due to Lead Contamination

    Crider Foods is recalling approximately 684,774 pounds of canned beef with gravy products due to possible unsafe levels of lead from a spice mix.

    Product
    Crider, Inc. — Crider Foods Recalls Canned Beef With Gravy Products Due to Possible Unsafe Levels of Lead From Outside Source
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V782000·2021-10-07

    GM Recalls Buick Enclave and Chevrolet Traverse for Air Bag Defect

    General Motors is recalling 2008-2017 Buick Enclave and 2013-2017 Chevrolet Traverse vehicles because the driver's air bag inflator may explode during deployment.

    Product
    BUICK — BUICK, CHEVROLET ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V783000·2021-10-07

    2022 Tiffin Phaeton Recreational Vehicle Electrical Wiring Defect

    Tiffin Motorhomes is recalling certain 2021-2022 Phaeton recreational vehicles due to an electrical outlet not properly installed during manufacturing, creating an open electrical wire inside the wall that could increase the risk of fire.

    Product
    TIFFIN — TIFFIN PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22701·2021-10-07

    Joovy Zoom 360 Ultralight Jogging Strollers Recalled for Fall Hazard

    Joovy is recalling about 9,200 Zoom 360 Ultralight jogging strollers because the front wheel bearing can fail or detach, creating a fall hazard. The company is offering a free repair kit.

    Product
    Zoom 360 Ultralight jogging strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2582-2021·2021-10-06

    Ultrasound Gel Products Recalled for Possible Bacterial Contamination

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. The FDA recommends healthcare providers stop using these products immediately.

    Product
    Norco Ultrasound Gel, Item/Description: NC70479/Norco Ultrasound Gel, 250 mL; NC70479/North Coast Ultrasound Gel, 250 mL; NC70479-5/Norco Ultrasound Gel, 5 liters; NC70479-5/North Coast Ultrasound Gel, 5 liters; NC70479-5C/Norco Ultrasound Gel, 5 liters (4); NC70479-5C/North…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2592-2021·2021-10-06

    Atrium Pneumostat Chest Drain Valve Recalled Following Fatal Preterm Infant Case

    Atrium Medical Corporation is recalling 92,430 units of its Pneumostat Chest Drain Valve after a preterm infant died during treatment with the device. The company is revising product labeling and warnings.

    Product
    Atrium Pneumostat Chest Drain Valve, Part Number 16100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0845-2021·2021-10-06

    Neutrogena Beach Defense Sunscreen Spray Recalled for Benzene Contamination

    Johnson & Johnson Consumer, Inc. is recalling Neutrogena Beach Defense water+sun protection sunscreen spray (SPF 60+) in 8.5 oz aerosol cans due to the presence of benzene contamination.

    Product
    Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 60+, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%) NET WT. 8.5 OZ. (240 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0844-2021·2021-10-06

    Neutrogena Beach Defense Sunscreen Spray Recalled for Benzene Contamination

    Johnson & Johnson Consumer, Inc. is recalling Neutrogena Beach Defense water+sun protection sunscreen spray (SPF 50) due to the presence of benzene contamination. The recall affects 1,437,804 aerosol cans distributed nationwide.

    Product
    Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 50, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT. 6.5 OZ. (184 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11254…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2577-2021·2021-10-06

    Reperfusion Catheter Recalled Due to Risk of Distal End Fracture

    Imperative Care ZOOM 71 Reperfusion Catheters are recalled due to potential for distal end fracture and detachment. This FDA Class I recall affects units distributed nationwide.

    Product
    Imperative Care, ZOOM 71 Reperfusion Catheter, REF: ICRC071137, TRX Tip, 137 cm, 6F (.083 in/2.11 mm), .071 in/1.8 mm), STERILE.EO, Rx Only, UDI: (01) 00812212030191. For neurovascular procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V779000·2021-10-06

    Mercedes-Benz Recalls 2021 Sprinter Vans for Electrical Fire Risk

    Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter vans because a cable duct defect may cause an electrical short, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2583-2021·2021-10-06

    Ultrasound Gels and Lotions Recalled Due to Bacterial Contamination Risk

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical may contain bacterial contamination. The FDA issued a Class I recall on August 18, 2021.

    Product
    EcoLotion Transmission Lotion, used in ultrasound procedures. Item/Description: NC70481/Eco Lotion 5 liters, NC70482/Eco Lotion with Aloe 5 liters, NC70482C/Eco Lotion with Aloe 5 liters (4); Myossage Lotion, 1 Gallon, Item: NC31208
    Category
    Medical Device
    Distribution
    Distributed nationwide