The Recall Desk

State

American Samoa product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31951–31975 of 73762

  • HighFDA (Drugs)·D-0062-2020·2019-10-09

    KRS Global Biotechnology Recalls Hydroxocobalamin Vials Due to Sterility Concerns

    KRS Global Biotechnology is recalling 345 vials of Hydroxocobalamin 10 mg/20 mL due to a lack of assurance of sterility. The recall covers all lots remaining within expiry and is distributed nationwide.

    Product
    Hydroxocobalamin 10 mg/20 mL (0.5 mg/mL) 20 mL fill in a 30 mL Vial, Rx Only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321678337
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0100-2020·2019-10-09

    Sermorelin and GHRP-2 Lyophilized Vials Recalled Due to Sterility Concerns

    KRS Global Biotechnology is recalling 120 vials of Sermorelin and GHRP-2 because the company cannot assure the products are sterile.

    Product
    Sermorelin, 3 mg / GHRP-2, 3 mg / Vial, For SC Use-Lyophilized, Rx Only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321674092
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0018-2020·2019-10-09

    Implant Direct Sybron Recalls Mislabeled Dental Implant Vials

    Implant Direct Sybron Manufacturing is recalling 22 vials of dental implants due to incorrect part numbers on the vial caps.

    Product
    ImplantDirect Legacy 3 Implant, REF 855216, SBM implant assembly, 2mmD x 16mmL, 4.5mmD platform, Rx, Sterile. The mislabeled model/part number on the vial cap is 835216. The responsible firm on the label is Implant Direct Sybron Manufacturing LLC, Thousand Oaks, CA.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0119-2020·2019-10-09

    Alkermes Recalls Vivitrol Kits Due to Needle Labeling Error

    Alkermes is recalling 16,231 Vivitrol kits because 1-inch needles were incorrectly placed in sleeves labeled for 1.5-inch needles. The drug vials are not affected.

    Product
    VIVITROL — VIVITROL (NALTREXONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2766-2019·2019-10-09

    Roche Accu-Chek Performa II Meters Recalled for Damaged Capacitor

    Roche Diabetes Care is recalling Accu-Chek Performa II meters because a damaged capacitor may cause short battery life or prevent the device from turning on.

    Product
    Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Aviva Plus Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertips, forearm, upper arm, or palm. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0001-2020·2019-10-09

    Metrix Secure EVA Dual Chamber IV Bags Recalled for Leaking Risk

    The Metrix Company is recalling 1,596 Secure EVA dual chamber IV bags due to a potential for leaking. The affected bags were distributed nationwide.

    Product
    SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 1500mL, (legless) REF 66615 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2762-2019·2019-10-09

    Zimmer Sidus Stem-Free Shoulder Humeral Head Recall for Incorrect Labeling

    Zimmer GmbH is recalling 19 Sidus Stem-Free Shoulder Humeral Head implants due to incorrect size labeling on the packaging.

    Product
    Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500 orthopedic implant - Product Usage: The Sidus Stem-Free Shoulder is designed for long-term implantation into the human shoulder joint as a total shoulder arthroplasty in combination with Zimmer or Biomet s…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2763-2019·2019-10-09

    Beckman Coulter Access Cortisol Reagent Recalled for Cross-Contamination

    Beckman Coulter is recalling Access Cortisol Reagent due to cross-contamination that may cause falsely decreased patient results.

    Product
    The Access Cortisol Reagent. REF (Catalog Number) 33600, Lot 831755. A paramagnetic particle, chemiluminscent immunoassay. Product Usage: The assay is a paramagnetic particle, chemiluminescent immunoassay for the quanitative determination of cortisol levels in human serum…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2765-2019·2019-10-09

    Roche Recalls Accu-Chek Aviva II Meters Due to Damaged Capacitor

    Roche Diabetes Care is recalling 26,600 Accu-Chek Aviva II meters because a damaged capacitor may cause short battery life or prevent the device from turning on.

    Product
    Accu-Chek Aviva II Meter - Product Usage: a. The Accu-Chek Aviva Plus Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertips, forearm, upper arm, or palm. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0066-2020·2019-10-09

    Labetalol HCl syringes are recalled due to lack of sterility assurance

    The FDA is recalling 6,405 units of Labetalol HCl single-dose syringes because there was insufficient assurance of sterility during production. No illnesses or injuries have been reported.

    Product
    Labetalol HCl 5 mg/mL 20 mg/4 mL (5 mg/mL) 4 mL Fill in a 6 mL Single Dose Syringe, Rx only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321676419
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0029-2020·2019-10-09

    CooperSurgical Embryology Heated Plate Recall Due to Touchpad Malfunction

    CooperSurgical is recalling 60 Embryology Heated Plates within the RI Witness system because the touchpad may not work properly after cleaning.

    Product
    Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product Usage: RI Witness uses Radio Frequency Identification (RFID) to detect and monitor all activity in the IVF laboratory. The system helps mitigate the risk of human error…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2764-2019·2019-10-09

    ELITech Viva-ProE Systems Recalled for Software Malfunction

    ELITech Group B.V. is recalling 89 Viva-ProE Systems because a software malfunction causes the devices to become inoperable.

    Product
    Viva-ProE Systems, Model # 6003-670, UDI: 03661540600357 - Product Usage: The ELITech Clinical Systems Selectra ProM is an automated clinical chemistry system intended for use in clinical laboratories. It is intended to be used for a variety of assay methods that have been…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V716000·2019-10-08

    2019 Mercedes-Benz and Freightliner Sprinter Door Component Recall

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because an incorrectly installed door component may make doors harder to open after a severe frontal crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER 4500, SPRINTER 3500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V715000·2019-10-08

    Mercedes-Benz Recalls Metris Vans Due to Exposed Battery Fire Risk

    Daimler Vans USA is recalling 2016-2019 Mercedes-Benz Metris vehicles because the backup battery compartment may lack a cover, creating a fire hazard if conductive material contacts the terminals.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20008·2019-10-08

    IKEA Recalls MATVRÅ Infant Bibs Due to Choking Hazard

    IKEA is recalling MATVRÅ infant bibs because the neck snaps can detach, posing a choking hazard to young children. No injuries have been reported.

    Product
    MATVRÅ Infant Bibs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20007·2019-10-08

    Ronson Tech Torch Auto Start Recalled by Zippo Due to Fire Hazard

    Zippo is recalling Ronson Tech Torch Auto Start lighters because they may continue to produce a flame after being turned off, posing a fire hazard.

    Product
    Ronson Tech Torch Auto Start
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V714000·2019-10-08

    Thor Motor Coach Recalls Motorhomes with Incorrect Capacity Labels

    Thor Motor Coach is recalling specific 2014-2020 motorhome models because incorrect carrying capacity labels may allow vehicles to be overloaded, increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH CITATION, SIESTA, QUANTUM, FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V711000·2019-10-07

    Freightliner Recalls 2018-2020 Cascadia Trucks for ABS Warning Light Defect

    Daimler Trucks North America is recalling 2018-2020 Freightliner Cascadia trucks because the ABS warning light may fail to illuminate during low-voltage starts, potentially leaving drivers unaware of a malfunction.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V707000·2019-10-04

    Blue Bird Recalls School Buses Due to Insufficient Roof Rivets

    Blue Bird is recalling 2019-2021 school buses because insufficient roof rivets may allow roof sheets to separate in a crash, increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, ALL AMERICAN SCHOOL BUS, VISION, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V708000·2019-10-04

    Outdoors RV Recalls Trail Series Trailers Due to Axle Mounting Defect

    Outdoors RV is recalling 2019-2020 Trail Series MTN TRX 22TRX toyhauler travel trailers because incorrectly mounted axles may cause unsafe towing conditions.

    Product
    OUTDOORS RV — OUTDOORS RV TRAIL SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V712000·2019-10-04

    Thomas Built Buses Recall 2014-2020 Models for Seat Impact Absorption Defect

    Daimler Trucks North America is recalling 2014-2020 Thomas Built school buses because specific seats may lack sufficient impact absorption, increasing injury risk in crashes.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, SAF-T-LINER C2, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20005·2019-10-04

    SPRI Ultra Heavy Resistance Bands Recalled for Injury Hazard

    Fit for Life is recalling SPRI Ultra Heavy Resistance Bands because they can separate from handles and strike users, causing injuries.

    Product
    SPRI Ultra Heavy Resistance Bands
    Category
    Consumer Product
    Distribution
    Distributed nationwide