The Recall Desk

State

American Samoa product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51651–51675 of 73858

  • SevereNHTSA·15V627000·2015-10-07

    Volkswagen Recalls 2015 Jetta, Golf, and E-Golf for Air Bag Defect

    Volkswagen is recalling 993 model year 2015 Jetta, Golf, and E-Golf vehicles because the passenger air bag may not deploy properly in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, E-GOLF, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1833-2015·2015-10-07

    Medistat RX Recalls Sterile Products Due to Sterility Assurance Concerns

    Medistat RX L.L.C. is recalling all sterile products, including various injectable medications, due to a lack of assurance of sterility.

    Product
    All Products Intended to be Sterile, mediStat Pharmacy, 110 East Azalea Ave., Foley, AL 36535, 844*737*2550. An Incomplete List of Recalled Products Includes 1) All Cyanacobalamin Products, 2) All Magnesium Chloride Products, 3) All Lipostat (MIC B12) Products, 4) All Trimix…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3248-2015·2015-10-07

    General Mills Recalls Cascadian Farm Organic Cut Green Beans for Listeria

    General Mills is recalling specific lots of Cascadian Farm Organic Cut Green Beans because one package tested positive for Listeria monocytogenes.

    Product
    Cascadian Farm Organic Cut Green Beans, Net Wt. 10 oz (284g) Keep Frozen.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0003-2016·2015-10-07

    Biosense Webster Recalls SOUNDSTAR eco Diagnostic Ultrasound Catheters

    Biosense Webster is recalling SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters because the ultrasound image may disappear if the CARTO 3 system restarts during a pericardial effusion.

    Product
    SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters. For intra-cardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2824-2015·2015-10-07

    Medtronic Navigated Solera Screwdrivers Recalled for Potential Tip Deformation

    Medtronic Navigation is recalling 2,346 Navigated Solera Screwdrivers used in spine surgery because specific use conditions may cause the tips to deform or break.

    Product
    P/N: 9734856, SCREWDRIVER, 9734856, SOLERA STD MAST; P/N: 9734857, SCREWDRIVER, 9734857, SOLERA RDN MAST; P/N: 9734279, SCREWDRIVER 9734279 SOLERA STANDARD; and P/N: 9734373, SCREWDRIVER 9734373 SOLERA REDUCTION. The Medtronic Navigated Solera Screwdrivers are reusable devices…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0002-2016·2015-10-07

    Biosense Webster Recalls Carto 3 EP Navigation System Due to Image Loss

    Biosense Webster is recalling the Carto 3 EP Navigation System because the ultrasound image may disappear during use, requiring a system restart.

    Product
    Carto 3 EP Navigation System. Electro physiology system which views of the electrical activity of the heart through real-time data on 3-D, color-coded cardiac maps.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V630000·2015-10-07

    Volvo Recalls 2015-2016 Trucks for Headlight Intensity Defect

    Volvo is recalling 2015-2016 VAH and VHD trucks because some headlights do not meet federal intensity requirements, increasing crash risk.

    Product
    VOLVO — VOLVO VAH, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3257-2015·2015-10-07

    KAL Amino Acid Complex Recalled for Undeclared Milk Allergen

    Nutraceutical International is recalling KAL Amino Acid Complex because the ingredient list does not explicitly state 'milk,' despite containing casein.

    Product
    KAL Brand Amino Acid Complex UPC 021245 51610 1, Product #51610
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·16701·2015-10-07

    BRP Recalls Youth Can-Am ATVs Due to Fuel Filter Fire Hazard

    BRP is recalling about 240 Youth Model Can-Am DS 90 and DS 90X ATVs because a fuel filter defect can cause leaks and fire. No injuries have been reported.

    Product
    Youth Model Can-Am all-terrain vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2823-2015·2015-10-07

    Medtronic Solera Screwdrivers Recalled for Tip Deformation Risk

    Medtronic Navigation is recalling 2,346 Solera screwdrivers used in spine surgery because specific conditions may cause the tips to deform or break.

    Product
    P/N: 9735023, DRIVER 9735023 SOLERA 5.5/6.0 MAS; P/N: 9735024, DRIVER 9735024 SOLERA 5.5/6.0 MAS CAN; P/N: 9735025, DRIVER 9735025 SOLERA 5.5/6.0 RMAS; P/N: 9735026, DRIVER 9735026 SOLERA 5.5/6.0 RMAS CAN; P/N: 9735027,DRIVER 9735027 SOLERA 5.5/6.0 FAS/SAS. The Medtronic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2822-2015·2015-10-07

    MicroAire LipoTower Recalled for Potential Electrical Shock Hazard

    MicroAire Surgical Instruments is recalling 168 LipoTower units due to a risk of electrical shock if internal lead wires detach and the ground connection fails.

    Product
    ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2826-2015·2015-10-07

    Ferno iNX Wheeled Stretcher Recalled for Telescoping Load Frame Defect

    Ferno-Washington Inc is recalling 72 Ferno iNX Wheeled Stretchers because hole elongation in the load frame may allow the retention pin to move.

    Product
    Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2821-2015·2015-10-07

    MicroAire LipoTower Recall Due to Electrical Shock Risk

    MicroAire Surgical Instruments is recalling three LipoTower units with aspiration pumps due to a potential risk of electrical shock if internal lead wires detach.

    Product
    ASP-1020 LipoTower with Aspiration Pump. Medical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2820-2015·2015-10-07

    Zimmer Recalls Guide Wires Due to Incorrect Expiration Date Labeling

    Zimmer, Inc. is recalling 112,568 sterile guide wires because the labels state a 10-year expiration date, while testing supports only 5 years.

    Product
    Zimmer Guide Wires for orthopedic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0004-2016·2015-10-07

    Lifeline Systems Recalls Philips GoSafe Mobile Help Button Due to Battery Issues

    Lifeline Systems is recalling 8,616 Philips GoSafe Mobile Help Button devices because irregular battery disconnection can cause charging issues.

    Product
    Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0005-2016·2015-10-07

    Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, DARK, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2819-2015·2015-10-07

    Sterilmed Recalls Reprocessed Zimmer Tourniquet Cuffs Due to Mislabeling

    Sterilmed is recalling 43 reprocessed Zimmer tourniquet cuffs because they are labeled as single hose but are actually dual hose devices.

    Product
    Zimmer, Reprocessed Zimmer Tourniquet Cuffs,34" Single Hose Single Bladder Brown (PLC), 34", Model (Reprocessor) Number: ZIM60-7075-106, Reprocessed by Sterilmed. Products are individually packaged in a Tyvek¿/poly pouch. There are 5 pouches placed inside a casepack box.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0001-2016·2015-10-07

    Guthy-Renker Recalls Rodan & Fields Proactiv Foundation for Subpotent Salicylic Acid

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, FAIR, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2818-2015·2015-10-07

    Olympus Recalls Gastrovideoscope Due to Insufficient Cleaning Accessory Information

    Olympus is recalling 1,014 EVIS EXERA II Gastrovideoscopes because specific cleaning accessories required for reprocessing were not provided.

    Product
    EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180; designed for endoscopic real-time ultrasound imaging, ultrasound guided needle aspiration and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0003-2016·2015-10-07

    Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, MEDIUM, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0004-2016·2015-10-07

    Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation

    Guthy-Renker LLC is recalling specific lots of Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, TAN, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0002-2016·2015-10-07

    Rodan & Fields Proactiv Foundation Recalled for Subpotent Salicylic Acid

    Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.

    Product
    Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, LIGHT, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D1834-2015·2015-10-07

    Apotex Recalls Verapamil Hydrochloride Extended-Release Tablets for Dissolution Failure

    Apotex Inc. is recalling 2,075 bottles of Verapamil Hydrochloride Extended-Release tablets, 240 mg, because one lot failed to meet dissolution specification limits.

    Product
    Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by Apotex Research Private Limited, Bangalore, Karnataka 560 099, India; Manufactured for: Apotex Corp., Weston, FL 33326. NDC 60505-2742-5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V625000·2015-10-06

    Winnebago and Itasca Motorhomes Recalled for Liquid Propane Hose Fire Risk

    Winnebago is recalling 2013-2016 Era, Trend, Tour, Journey, and Itasca motorhomes because a liquid propane hose may harden and leak, increasing fire risk.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA TREND, TOUR, JOURNEY, ERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E082000·2015-10-06

    Dorman Aftermarket Steering Shafts Recalled for Potential Separation Risk

    Dorman is recalling aftermarket steering shafts for 1995-2002 Ford, Mercury, and Lincoln vehicles because they may separate, causing loss of steering control.

    Product
    MERCURY — MERCURY, FORD, LINCOLN GRAND MARQUIS, CROWN VICTORIA, TOWN CAR
    Category
    Vehicle
    Distribution
    Distributed nationwide