The Recall Desk

State

American Samoa product recalls

73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26851–26875 of 73595

  • SevereFDA (Drugs)·D-0072-2021·2020-11-18

    H & H Remedies Recalls White Liniment Due to CGMP Deviations

    H & H Remedies, LLC is voluntarily recalling 365 bottles of White Liniment due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    White Liniment packaged in a) 1 oz; b) 4 oz.; and c) 6 oz bottles. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V715000·2020-11-18

    Keystone Outback trailers recalled for potential frame rail buckling defect

    Keystone is recalling 2019–2021 Outback recreational trailers for inadequate frame rail support that may cause buckling and crash risk. Owners should contact 1-866-425-4369 for the free frame reinforcement repair.

    Product
    KEYSTONE — KEYSTONE OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V713000·2020-11-18

    Lamborghini Recalls 2019-2020 Urus Vehicles Due to Fuel Line Fire Risk

    Lamborghini is recalling 2,831 2019-2020 Urus vehicles because high engine temperatures may damage the fuel line connector, causing a leak and increasing fire risk.

    Product
    LAMBORGHINI — LAMBORGHINI URUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0431-2021·2020-11-18

    Stryker Recalls Cranial Perforators Due to Potential Metal Fragment Risk

    Stryker is recalling Zyphr Disposable Cranial Perforators because a crack in the inner bit could release metal fragments into the surgical site or cause delayed disengagement.

    Product
    Stryker Zyphr Disposable Cranial Perforator, Large 14/11 mm- is a sterile, single use cutting accessory intended for cutting an 11 mm diameter access hole through the cranium of adult patients. Catalog Number: 5100-060-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0076-2021·2020-11-18

    Baxter Recalls Bupivacaine Injection Due to Particulate Matter

    Baxter Healthcare is recalling specific lots of Bupivacaine Hydrochloride Injection due to the presence of black and transparent particles in the solution.

    Product
    Bupivacaine Hydrochloride in 8.25% Dextrose Injection, USP Spinal 0.75% (15 mg/2 mL) 10 x 2 mL single-dose ampules, Rx only, Manufactured for: Baxter Healthcare Corporation Deerfield, IL 60015 USA, Manufactured by: Baxter Pharmaceuticals India Private Ltd Ahmedabad 382213 India…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0439-2021·2020-11-18

    Fresenius Liberty Select Cycler Software Recall for Inadequate Dialysis Risk

    Fresenius Medical Care is recalling Liberty Select Cycler devices with software version 2.9.0 because a software error may cause the device to fail to recognize extra fluid, potentially leading to inadequate dialysis.

    Product
    Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and RTLR180343
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0446-2021·2020-11-18

    United Imaging uCT 550 CT Scanners Recalled for Timer Display Error

    Shanghai United Imaging Healthcare is recalling five uCT 550 CT scanners because an incorrect delay timer display may expose operators to unnecessary radiation.

    Product
    Computed Tomography X-Ray System, Model uCT 550, Rx, CE, GTIN: 06971576831036 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0445-2021·2020-11-18

    United Imaging uCT 530 CT Scanner Recalled for Incorrect Timer Display

    Shanghai United Imaging Healthcare Co., Ltd. is recalling four uCT 530 CT scanners because an incorrect delay timer may display, potentially exposing operators to unnecessary radiation.

    Product
    Computed Tomography X-Ray System, Model uCT 530, Rx, CE, GTIN: 06971576831012 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0427-2021·2020-11-18

    Boston Scientific AMS 700 MS Pump Recall for Activation Difficulties

    Boston Scientific is recalling AMS 700 MS Pumps due to reports of difficulty activating the device to inflate cylinders.

    Product
    AMS 700 MS Pump with and without InhibiZone, sold as individual units and also pre-connected to AMS 700 cylinders. Inflatable Penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0447-2021·2020-11-18

    United Imaging uCT 760 CT Scanner Recalled for Timer Display Error

    Shanghai United Imaging Healthcare is recalling five uCT 760 CT scanners because a display error may cause operators to receive unnecessary radiation exposure.

    Product
    Computed Tomography X-Ray System, Model uCT 760, Rx, CE, GTIN: 06971576831043 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0448-2021·2020-11-18

    United Imaging uMI 550 PET/CT System Recalled for Incorrect CT Scan Delay Timer

    Shanghai United Imaging Healthcare is recalling nine uMI 550 PET/CT systems because an incorrect CT scan delay timer may display, potentially exposing operators to unnecessary radiation.

    Product
    Positron Emission Tomography and Computed Tomography System, Model uMI 550, Rx, CE, GTIN: 06971576832026 - Product Usage: intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0443-2021·2020-11-18

    Maquet BMU 40 Blood Monitoring Units Recalled for Electrical Safety Non-Compliance

    Maquet Cardiovascular is recalling 51 Blood Monitoring Units (BMU 40) because the printed circuit boards do not meet IEC electrical safety standards for creepage distance.

    Product
    Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during cardiopulmonary bypass (CPB) or similar procedures with extracorporeal circulation, which require continuous monitoring of the arterial and/or venous blood parameters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V716000·2020-11-18

    2021 Volkswagen Atlas and Select Models: Rear Camera Malfunction Risk

    Volkswagen is recalling certain 2021 Atlas and related models because the rear view camera may malfunction during startup, showing a black screen or frozen image, reducing visibility when reversing and increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ARTEON, GOLF, JETTA, TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0114-2021·2020-11-18

    Starwest Botanicals Recalls Organic Elderberry Tea Due to Salmonella Risk

    Starwest Botanicals is recalling specific lots of organic elderberry tea after a customer test detected Salmonella.

    Product
    Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia 1 lb. and 4 oz. Distributed in Mylar bags. 1 lb. UPC: 7 67963 07315 0; Item # 209290-01 4 oz. UPC 7 67963-10561-5; Item # 209290-04 Daily serving size; Pour 8-12 oz. of boiling water (212 degrees F) over 1 tsp…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0069-2021·2020-11-18

    Teva Recalls Mesalamine Tablets Due to Failed Dissolution Testing

    Teva Pharmaceuticals is recalling 133,829 bottles of Mesalamine Delayed-Release Tablets because stability testing revealed out-of-specification dissolution results.

    Product
    MESALAMINE — MESALAMINE (MESALAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0070-2021·2020-11-18

    AvKARE Recalls Mesalamine Tablets for Failed Dissolution Specifications

    AvKARE Inc. is recalling specific lots of Mesalamine Delayed-Release Tablets because they failed to meet dissolution specifications.

    Product
    Mesalamine Delayed-Release Tablets, USP 1.2 gram (Once-Daily), 120 Tablets bottle, Rx Only Manufactured for: AvKARE, Inc. Pulaski, TN 38478 NDC 42291-564-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0444-2021·2020-11-18

    Aesthetics Biomedical Recalls Vivace Electrosurgical System for Regulatory Violation

    Aesthetics Biomedical is recalling 623 Vivace Electrosurgical Systems because a high-frequency output was not cleared for U.S. distribution.

    Product
    SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and surgical procedures for electrocoagulation and hemostasis, and the percutaneous treatment of facial wrinkles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0073-2021·2020-11-18

    H & H Remedies Recalls Vapor Ointment Due to Manufacturing Deviations

    H & H Remedies, LLC is voluntarily recalling 252 jars of Vapor Ointment due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Vapor Ointment packaged in a) 1/8 oz; b) 2 oz.; c) 4 oz.; and d) 8 oz jars. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0071-2021·2020-11-18

    H & H Remedies Recalls Union Salve Due to CGMP Deviations

    H & H Remedies, LLC is voluntarily recalling 939 jars of Union (black) salve due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Union (black) salve packaged in a) 1/8 oz; b) 2 oz.; c) 4 oz.; d) 8 oz.; e) 16 oz.; and f) 32 oz. jars. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E085000·2020-11-17

    Denso Recalls Fuel Pumps Due to Impeller Cracking and Engine Stalling Risk

    Denso is recalling fuel pumps where an impeller may crack and deform, causing the pump to fail. This failure can cause the engine to stall while driving, increasing the risk of a crash.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V711000·2020-11-17

    Thor Motor Coach Motorhomes Electrical Fire Risk Battery Isolation Recall

    Thor Motor Coach is recalling certain 2020-2021 motorhomes. A faulty Battery Isolation Manager/Relay allows water into the engine compartment, creating electrical arcing and fire risk. Owners should contact TMC at 1-877-855-2867.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, DAYBREAK, FOUR WINDS, QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V708000·2020-11-17

    Altec Recalls AH150 and AH125 Aerial Devices Due to Valve Defect

    Altec is recalling 2006-2020 AH150 and AH125 aerial devices because an incorrect counterbalance valve may cause the boom to lower unexpectedly, increasing injury risk.

    Product
    ALTEC — ALTEC AH125, AH150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V712000·2020-11-17

    Volkswagen Atlas Vehicles Recalled for Steering Knuckle Damage

    Volkswagen is recalling certain 2021 Atlas and 2020-2021 Atlas Cross Sport vehicles with damaged steering knuckles that may fail during operation. A failed steering knuckle can cause loss of steering control, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide