State

American Samoa product recalls

73,187 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 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14526–14550 of 73212

SevereFDA (Food)·F-1366-2023·2023-08-16
Energy balls recalled for undeclared sesame allergen
Betty Lou's Paleo Java Nuts About Energy Balls are being recalled due to undeclared sesame in the product. The recall affects packages distributed nationwide.
Product
Betty Lou's Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds, shelf-stable, 12-month shelf life, 1.5 oz (42g) package and 12/1.5 oz. packages per display box. Packages are sold individually (UPC 0 1607352146 5) or packaged into 12-ct display box (UPC 0…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2341-2023·2023-08-16
Olympus LF-P Tracheal Intubation Fiberscope Sterilization and Compatibility Update
Olympus is updating labeling for 686 LF-P fiberscopes to clarify they are no longer compatible with OER reprocessors and specify new 100% ETO sterilization protocol.
Product
Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Olympus Light Source, documentation equipment, display monitor and other ancillary equipment for management of Endotracheal Tube
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2355-2023·2023-08-16
LINK MP Hip Stem Trial Instruments difficult to remove after implantation
The LINK MP Monoblock hip stem trial instruments may require increased force to remove after implantation, potentially prolonging surgery or requiring modification of the surgical procedure.
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 24 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-24/00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2366-2023·2023-08-16
Medline Total Hip Kit Recalled for Expired Prep Solution
Medline is recalling the Total Hip Kit (REF DYNJ903275S) because the included prep solution expires before the kit itself expires. Sixteen kits with lot code 23CDC733 were distributed nationwide.
Product
Total Hip Kit, REF DYNJ903275S; surgical convenience kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2354-2023·2023-08-16
LINK MP Monoblock Hip Stem trial instruments recalled for increased removal difficulty
Waldemar Link GmbH recalled LINK MP Monoblock hip stem trial instruments (Size 23) nationwide due to increased force required for removal post-impaction, potentially prolonging surgery time.
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 23 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-23/00
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V583000·2023-08-16
Triumph Tiger Sport 660 Motorcycles Recalled for Engine Stall Risk
Triumph is recalling 2022-2024 Tiger Sport 660 and Trident 660 motorcycles because the MAP hose may become obstructed, causing incorrect engine readings, stalling, and crash risk. Dealers will replace the hose for free.
Product
TRIUMPH — TRIUMPH redundant TRIDENT 660, TIGER SPORT 660
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2347-2023·2023-08-16
LINK MP Monoblock Hip Stem Trial Instruments May Require Increased Removal Force
LINK MP Monoblock Hip Stem trial instruments may require increased force to remove after impaction, potentially prolonging surgery for affected patients.
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 16 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-116/00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2351-2023·2023-08-16
Hip implant trial stem: increased removal force may extend surgery
Waldemar Link is recalling LINK MP Monoblock Hip Stem trial instruments due to increased force required for removal during surgery, which may prolong the procedure or require modification.
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 20 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-120/00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2356-2023·2023-08-16
LINK MP Monoblock Hip Stem Trial Instruments Difficult to Remove After Impaction
Waldemar Link is recalling LINK MP Monoblock Hip Stem trial instruments because they may require increased force to remove after impaction, potentially prolonging surgery or requiring procedural modification.
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 25 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-25/00
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V584000·2023-08-16
BMW vehicles with defective seat belt warning software recalled
BMW is recalling 2019-2022 330i, M340i, and other models due to receiver audio module software that may fail to generate proper seat belt warnings, increasing crash injury risk.
Product
BMW — BMW M340I, 228I, M440I, 330I
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2345-2023·2023-08-16
Hip Stem Trial Implant May Require Excessive Force During Removal
A trial hip stem implant may require excessive force to remove after insertion during surgery, potentially prolonging the procedure or requiring surgical modification.
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 14-Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 136-114/00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2352-2023·2023-08-16
LINK MP Hip Stem trial instruments may require increased removal force during surgery
LINK MP Monoblock hip stem trial instruments may require increased force to remove during surgery, potentially prolonging procedures or requiring surgical modification.
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 21 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-121/00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2344-2023·2023-08-16
Olympus Endoscope Reprocessor Labeling Revised for Compatibility and Sterilization Parameters
Olympus is revising labeling for its OER-Elite, OER-Pro, and OER-Mini endoscope reprocessors due to incompatible endoscope models and incorrect sterilization parameters in previous labeling. The revisions remove two endoscope models from the compatibility list and correct gas sterilization concentration requirements.
Product
Olympus Endoscope Reprocessor OER-Elite-For use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes and their accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2393-2023·2023-08-16
Ellacor System recalled for bearing adhesive defect risk
The FDA is recalling 127 Ellacor System devices for a potential bearing adhesive failure in the handpiece. The defect could cause core overlap, leading to prolonged healing and scarring.
Product
ellacor System with Micro-Coring Technology-Indicated for use by medical professionals for the treatment of moderate and severe wrinkles in the mid and lower face in adults aged 22 years or older with Fitzpatrick skin types I-IV. Model #: Gen 4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2359-2023·2023-08-16
Siemens ARTIS Icono Biplane Angiography Systems Thermal Cable Connector Defect
Siemens recalls ARTIS icono biplane angiography systems with defective cable connectors that may cause thermal overload, burning smell, and loss of imaging functionality during clinical procedures.
Product
ARTIS icono biplane -Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Material Number: 11327600
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2340-2023·2023-08-16
Olympus VISERA Tracheal Videoscope reprocessor compatibility and sterilization procedure revision
Olympus is revising labeling for the VISERA Tracheal Intubation Videoscope to correct equipment compatibility information and update sterilization procedures. The device is no longer compatible with OER-Pro, OER-Elite, and OER-Mini reprocessors; sterilization and cleaning procedures have changed significantly.
Product
VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V- For airway management which includes endoscopic observation to access airway anatomy, endotracheal/endobronchial intubation and management.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2357-2023·2023-08-16
VITROS Troponin I ES Immunodiagnostic Reagent Pack Recalled for Incorrect Wells
ORTHO-CLINICAL DIAGNOSTICS is recalling VITROS Troponin I ES Reagent Pack due to potential incorrect wells that could generate false negative diagnostic results. Lot 4800 with expiration 10-Jun-2023 is affected.
Product
VITROS Immunodiagnostic Products Troponin I ES Reagent Pack
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2350-2023·2023-08-16
Hip stem trial instruments recalled due to excessive removal force
LINK MP Monoblock hip stem trial instruments may require excessive force to remove after impaction, potentially prolonging surgery or requiring procedural modification.
Product
LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 19-Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-119/00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2360-2023·2023-08-16
Angiography systems recalled due to thermal overload in cable connectors
Siemens ARTIS icono floor angiography systems may experience thermal overload in cable connectors during fluoroscopy, causing burning smell and loss of imaging capability. The recall affects 7 units worldwide.
Product
ARTIS icono floor-Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Material Number: 11327700
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2397-2023·2023-08-16
Philips MR 7700 Magnetic Resonance System Smoke Detector Interlock Bypass
Philips MR 7700 MRI systems can have their smoke detector interlock safety mechanism bypassed when power cycled after smoke detection, allowing continued operation despite potential fire hazards.
Product
MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2362-2023·2023-08-16
Randox Urea Enzymatic Assay Recall: Falsely Low Test Results Risk
FDA recalls Randox RX Series Urea test kits because carryover from prior LDL-cholesterol tests may produce falsely low results, up to 11% below accurate values, potentially delaying diagnosis.
Product
Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) UR3825 (2) UR3873 (3) UR8334 (4) UR8070 (Modena)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2342-2023·2023-08-16
Olympus OER-Pro Endoscope Reprocessor Revised Labeling for Equipment Compatibility
Olympus revised OER-Pro labeling because two endoscope models (LF-V, LF-P) are no longer compatible. Sterilization parameters and cleaning procedures have also changed.
Product
Olympus Endoscope Reprocessor OER-Pro-For use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes and their accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2364-2023·2023-08-16
Medical Device Recall: UroLift Visual Obturator Weld Defect Risk
The UroLift Visual Obturator has an improperly performed weld that may fracture during use, and the welded area can harbor contamination not removed by standard cleaning. Affected units should not be used.
Product
UroLift Visual Obturator, 20Ch-The visual obturator is used with the UroLift¿ system. Instrument for insertion of a cystoscope shaft into the bladder. Model: UL-VO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2395-2023·2023-08-16
MR Imaging System Smoke Detector Interlock Vulnerable to Bypass via Power Cycling
Philips Ingenia Elition X MR systems can have their smoke detection safety interlock bypassed by power cycling the equipment. This vulnerability could allow unsafe operation during hazardous conditions.
Product
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V585000·2023-08-16
Polar Tank Trailer SCX9 Recalled for Missing Rear Impact Guard Plate
Entrans is recalling 2023 Polar Tank SCX9 trailers that may lack a rear impact guard certification plate, failing federal safety standards.
Product
POLAR — POLAR TANK TRAILER SCX9
Category
Vehicle
Distribution
Distributed nationwide