The Recall Desk

State

American Samoa product recalls

73,118 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 73,118 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14026–14050 of 73143

  • HighFDA (Drugs)·D-0022-2024·2023-10-11

    Fentanyl Injection Recalled Due to Lack of Sterility Assurance

    Central Admixture Pharmacy Services Inc is recalling 240 units of 100 mL bags of fentanyl 2500 mcg/50 mL due to lack of assurance of sterility. The product was distributed nationwide.

    Product
    fentaNYL, 2500 mcg/50 mL, (50 mcg/mL), 100 mL bag, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0029-2024·2023-10-11

    HYDROmorphone Syringes Recalled for Lack of Sterility Assurance

    Central Admixture Pharmacy Services is recalling 4,550 syringes of HYDROmorphone due to lack of assurance of sterility. The product was distributed nationwide.

    Product
    HYDROmorphone in 0.9% sodium chloride, 15 mg/30 mL, (0.5 mg/mL), 30 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2011-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0033-2024·2023-10-11

    Dr. Berne's MSM Drops Recalled Due to Manufacturing Practice Deviations

    Dr. Berne's MSM DROPS is being recalled due to manufacturing practice deviations. The recall involves 6,060 bottles distributed nationwide and internationally.

    Product
    Dr. Berne's MSM DROPS 15% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, [email protected], UPC 00854582001036
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0039-2024·2023-10-11

    HydrALAZINE Hydrochloride Tablets recalled due to impurity specifications failure

    Amerisource Health Services LLC is recalling HydrALAZINE Hydrochloride Tablets, 10 mg, nationwide due to impurities exceeding specifications in a repackaged product batch.

    Product
    HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC#: 68084-447-01; Individual Dose NDC: 68084-447-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0034-2024·2023-10-11

    Dr. Berne's MSM MIST 15% Topical Spray Recalled for Manufacturing Deviations

    Dr. Berne's Whole Health Products has voluntarily recalled Dr. Berne's MSM MIST 15% Solution (30 mL bottles) due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing. The recall affects 795 bottles distributed nationwide and internationally.

    Product
    Dr. Berne's MSM MIST 15% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, [email protected].
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0036-2024·2023-10-11

    Drug Recall: Dr. Berne's MSM Drops for Manufacturing Practice Violations

    Dr. Berne's MSM DROPS 5% Solution is being recalled due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall affects 3833 bottles distributed nationwide and internationally.

    Product
    Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, [email protected], UPC 00854582001111.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0038-2024·2023-10-11

    Oxybutynin Extended-Release Tablets Recalled for Failed Dissolution Specifications

    Zydus Pharmaceuticals recalls Oxybutynin Chloride Extended-Release Tablets 10 mg nationwide because the medication failed dissolution specifications. Affected lot numbers: M300652 and M300651.

    Product
    OXYBUTYNIN — OXYBUTYNIN (OXYBUTYNIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2648-2023·2023-10-11

    Siemens MAGNETOM headphones may create artifacts during MRI imaging

    Siemens Medical Solutions is recalling over-ear headphones used with MAGNETOM MRI systems. Lubricating grease in the headband may cause visible imaging artifacts during head examinations.

    Product
    (1) Over-ear headphones used with the MAGNETOM Amira MAGNETOM Free.Star MAGNETOM Sempra, MAGNETOM Free.Max, MAGNETOM Mica MAGNETOM Spectra Siemens Model Number:11060845 Used with the following MAGNETOM MRI Systems: MAGENTOM Amira 10836777 & 10838610; MAGENTOM Free.Max…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2657-2023·2023-10-11

    Medtronic Restore Clinician Programmer software recalled for compatibility issue

    Medtronic is recalling Restore Clinician Programmer Application Software due to compatibility issues with legacy software that prevent communication with implanted neurostimulators. The recall affects 2,408 devices worldwide.

    Product
    Restore Clinician Programmer Application Software, model number A71100, used with the Restore Neurostimulators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V678000·2023-10-09

    Lightning eMotors Recalls FT3 Vehicles for Instrument Cluster Warning Light Defect

    Lightning eMotors is recalling 239 FT3-40, FT3-80, and FT3-120 vehicles because the instrument cluster may fail to activate brake, park, and ABS warning lights during startup.

    Product
    LIGHTNING EMOTORS — LIGHTNING EMOTORS FT3-40, FT3-80, FT3-120
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V676000·2023-10-06

    Mercedes-Benz Recalls 2022-2023 AMG SL55 and SL63 for Wiring Defect

    Mercedes-Benz is recalling 2022-2023 AMG SL55 and SL63 vehicles because an improperly secured electrical wiring harness may overheat or cause a short circuit, increasing the risk of fire or loss of drive power.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG SL55, AMG SL63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V675000·2023-10-06

    2020-2022 Ford Explorer Driveshaft Disconnection Risk

    Ford is recalling certain 2020-2022 Explorer vehicles because the rear axle mounting bolt may fracture, causing the driveshaft to disconnect. This can result in loss of drive power or vehicle rollaway, increasing crash risk.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V677000·2023-10-06

    Mercedes-Benz Recalls One 2022 EQB 350 for Child Seat Anchor Covers

    Mercedes-Benz is recalling one 2022 EQB 350 vehicle because incorrect child seat anchor covers may have been installed, potentially leading to improper child restraint installation.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQB 350 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24002·2023-10-05

    Cocco Candy Rolling Candy Recalled Due to Choking Hazard

    KGR Distribution Corp. recalls Cocco Candy Rolling Candy in multiple flavors because the candy's rolling ball can dislodge and pose a choking hazard. One death has been reported.

    Product
    Cocco Candy Rolling Candy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24701·2023-10-05

    Capri Blue Pet Products Recalled Due to Bacterial Contamination Risk

    CURiO Brands is recalling approximately 59,000 Capri Blue pet sprays and shampoos distributed from June through August 2023 because they can contain Pseudomonas aeruginosa bacteria, which poses a risk of serious infection to people with weakened immune systems or external medical devices.

    Product
    Capri Blue Pet Sprays and Shampoos
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V673000·2023-10-05

    Jayco Precept and Entegra Coach motorhomes: window shade emergency exit obstruction

    Jayco is recalling 2024 Precept and Entegra Coach Vision XL motorhomes because their window shades may obstruct emergency exit windows. Obstructed emergency exits could delay occupant evacuation during emergencies.

    Product
    ENTEGRA — ENTEGRA, JAYCO VISION XL, PRECEPT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24001·2023-10-05

    Candy Dynamics Recalls Slime Licker Sour Rolling Liquid Candy for Choking Hazard

    Candy Dynamics is recalling approximately 70 million Slime Licker Sour Rolling Liquid Candies because the rolling ball can detach from the container, posing a choking hazard to children. Two reports of ball detachment have been received with no injuries reported.

    Product
    Slime Licker Sour Rolling Liquid Candy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24004·2023-10-05

    Children's Blanket Sleepers and Robes Recalled for Burn Hazard

    International Intimates is recalling Rene Rofe Girl Children's Blanket Sleepers and Hooded Robes because they fail to meet federal flammability standards for children's sleepwear, posing a burn injury risk to children ages 6–14.

    Product
    Rene Rofe Girl Children's Blanket Sleepers and Hooded Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24003·2023-10-05

    Russound MCA-88 Multizone Controller Amplifiers Recalled for Fire Hazard

    Russound is recalling about 3,170 MCA-88 Multizone Controller Amplifiers because internal circuit board components can overheat and catch fire. The firm has received 16 reports of smoking, charring, and burning, though no injuries have been reported.

    Product
    Russound MCA-88 Multizone Controller Amplifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V671000·2023-10-04

    Volkswagen Recalls 2019 Atlas Vehicles Due to Driver Side Air Bag Defect

    Volkswagen is recalling 2019 Atlas vehicles because the driver's side air bag may be missing a weld, which could cause it to deploy improperly or detach in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E075000·2023-10-04

    Dorman Recalls Front Suspension Ball Joints Due to Steering Loss Risk

    Dorman Products is recalling specific front suspension ball joints because the ball stud may separate, leading to loss of steering control and increased crash risk.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide