State

American Samoa product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38951–38975 of 73766

SevereFDA (Food)·F-0978-2018·2018-04-04
Piggie Park Recalls Honey BBQ Sauces Due to Undeclared Soy and Wheat
Piggie Park Enterprises Inc. is recalling Maurice's Honey Southern Gold BBQ Sauce and Carolina Gold Honey Sauce because they contain undeclared soy and wheat ingredients.
Product
Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bottles; UPC Code 0 7561654332 6 and Carolina Gold Honey Sauce; Net Wt. 18 oz. bottle; UPC Code 0 7561654383 8
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1175-2018·2018-04-04
ConMed Mini Infant Radiotranslucent Electrodes Recalled for Adhesive Conductivity Issues
ConMed is recalling 18,720 Mini Infant Radiotranslucent Electrodes because adhesive on contact wires may impede conductivity and cause failure.
Product
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602H Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18V214000·2018-04-04
Ford Recalls 2018 F-Series and Expedition for Gear Shift Cable Defect
Ford is recalling 2018 F-650, F-750, F-150, and Expedition vehicles because a gear shift cable clip may not be seated, causing the transmission to be in a different gear than indicated.
Product
FORD — FORD EXPEDITION, F-150, F-750 SD, F-650 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V215000·2018-04-04
Zero Motorcycles Recalls 2012 Models Due to Battery Fire Risk
Zero Motorcycles is recalling 2012 S, DS, and DSP models because battery wear may cause electrical shorts and fire. Owners should stop riding and charging these vehicles.
Product
ZERO — ZERO ZERO S, ZERO DS, DSP
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1236-2018·2018-04-04
Zimmer Biomet Recalls Phoenix Nail System Inserter Connectors Due to Fracturing
Zimmer Biomet is recalling specific lots of Phoenix Nail System 3.5mm Inserter Connectors because they have fractured and remained in the device implant.
Product
Phoenix Nail System, intended for use with an intramedullary nail system for alignment, stabilization and fixation of fractures. 3.5mm Inserter Connector, Short; Model Number: 14-441045; Kit Model Numbers: 14-400082, 14-400082S, 14-440065S, 14-442000-00, 14-442000S…
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·18136·2018-04-04
Vornado VH101 Personal Vortex Electric Space Heaters Recalled for Fire and Burn Hazards
Vornado Air is recalling about 350,000 VH101 Personal Vortex electric space heaters because they can overheat, posing fire and burn hazards.
Product
VH101 Personal Vortex electric space heaters
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0610-2018·2018-04-04
Amneal Recalls Fosphenytoin Sodium Injection Due to Particulate Matter
Amneal Pharmaceuticals is recalling specific lots of Fosphenytoin Sodium Injection because of the presence of particulate matter.
Product
Fosphenytoin Sodium Injection, USP 500 mg PE*/10 mL, Made in India. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807, NDC 70121-1390-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1177-2018·2018-04-04
ConMed Pediatric Defibrillation Electrodes Recalled for Adhesive Conductivity Issues
ConMed is recalling 18,720 pediatric defibrillation electrodes because adhesive on contact wires may impede conductivity and cause failure.
Product
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Physio-Control¿ Quik-Combo" Connector, REF/Catalog Number 2602M Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1187-2018·2018-04-04
Cook Inc. Recalls Marrs Laparoscopic GIFT Catheters Due to Quality Testing Gaps
Cook Inc. is recalling 21 Marrs Laparoscopic GIFT Catheters because they were distributed without completed quality testing, posing a risk of nonviable embryos.
Product
Marrs Laparoscopic GIFT Catheters, Catalog Number:K-J-MLC-503000, Global Product Number: G18022 Product Usage: Used to place in vitro fertilized (IVF) embryos into the uterine cavity. Intended for one-time use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1225-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System because a device performance review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System ACE TROCH NAIL 125 DEG. X 11MM ACE TROCH NAIL 130 DEG. X 11MM ACE TROCH NAIL 135 DEG. X 11MM ACE TROCH NAIL 125 DEG. X 13MM ACE TROCH NAIL 130 DEG. X 13MM ACE TROCH NAIL 135 DEG. X 13MM The Trochanteric Nail System is intended to treat…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1226-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System because a Device Performance Review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System STER TROC END CAP STER TROC END CAP 5MM STER TROC END CAP 10MM STER TROC END CAP 15MM STER TROC END CAP 20MM STER TROC END CAP 25MM The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1228-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System after a device performance review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System STER TROC LAG SCR 70 MM The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures, intertrochanteric fractures, high subtrochanteric fractures and combinations of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1227-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System after a device performance review failed to meet clinical survivorship criteria.
Product
ACE Trochanteric Nail System STER TROC NAIL 125 DEG X 9MM STER TROC NAIL 130 DEG X 9MM STER TROC NAIL 135 DEG X 9MM The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures, intertrochanteric…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1208-2018·2018-04-04
Puritan Bennett 980 Ventilator Batteries Recalled for Firmware Defect
FDA is recalling 15,885 rechargeable lithium-ion batteries for Puritan Bennett 980 ventilators due to incorrect firmware that may prevent full charging.
Product
Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Ventilator System including Pediatric-Adult Ventilator, Neonatal Ventilator, Universal Ventilator; Battery Product Number: 10086042; UDI: 20884521700861 The rechargeable lithium-ion batteries are intended to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1178-2018·2018-04-04
ConMed Recalls Mini Infant Radiotranslucent Electrodes Due to Adhesive Defect
ConMed is recalling 18,720 Mini Infant Radiotranslucent Electrodes because adhesive on the contact wires may impede conductivity and cause failure.
Product
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, ZOLL¿ Connector, REF/Catalog Number 2602Z Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602 electrodes provide…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18E020000·2018-04-04
Badass Helmet Company Recalls Metalhead 2.5 Motorcycle Helmets for Safety Defect
Badass Helmet Company is recalling Metalhead 2.5 helmets because they may not adequately protect wearers in a crash, failing federal safety standards.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1230-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System after a Device Performance Review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System STER TROC NAIL 180X11X140 STER TROC NAIL 125 DEG X 11MM STER TROC NAIL 130 DEG X 11MM STER TROC NAIL 135 DEG X 11MM The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1237-2018·2018-04-04
Signia Power Handle Recalled for Shutting Down During Surgical Use
Covidien LLC is recalling 2,121 Signia Power Handles because they reportedly shut down during use. The devices are used in various surgical procedures.
Product
Signia" Power Handle (SIGPHANDLE, SIGNVAL1 and SIGVAL20 - Kits) The Signia" Power Handle, when used with Endo GIA" single-use reloads and Endo GIA" single-use reloads with Tri-Staple" Technology, has applications in open and minimally invasive general abdominal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1219-2018·2018-04-04
DePuy Sigma HP Cemented Trochlear Implants Recalled for Elevated Revision Rates
DePuy Orthopaedics is recalling specific Sigma HP Cemented Trochlear Implants due to elevated revision rates identified during post-market surveillance.
Product
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP Cemented Trochlea Size 2 Narrow Left, Catalog Number: 102403200, GTIN: 10603295001621; (3) Sigma HP Cemented Trochlea Size 3 Narrow Left, Catalog Number: 102403300…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1186-2018·2018-04-04
Cook Inc. Recalls IVF Intratubal Transfer Sets Due to Quality Testing Gaps
Cook Inc. is recalling specific lots of Echosight Jansen-Anderson Intratubal Transfer Sets because they were distributed without completed quality testing, posing a risk of nonviable embryos.
Product
Echosight Jansen-Anderson Intratubal Transfer Set, Catalog Number: K-J-JITS-572900, Global Product Number: G17946 Product Usage: Used to place in vitro fertilized (IVF) embryos into the uterine cavity. Intended for one-time use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1231-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System because a Device Performance Review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System TROCH NAIL ST 13X180 125DG STRL TROCH NAIL ST 13X180 130DG STRL TROCH NAIL ST 13X180 135DG STRL The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1259-2018·2018-04-04
Encore Medical Recalls Altivate Anatomic Pegged Glenoid Trial Instruments
Encore Medical is recalling 92 units of Altivate Anatomic Pegged Glenoid Trials because the peg base design is larger on the trials than on the implants.
Product
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 50mm, REF 804-07-500 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1233-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Screws
Zimmer Biomet is recalling ACE Trochanteric Nail System screws because a device performance review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System ATN AR SCREW 60MM STERILE ATN AR SCREW 65MM STERILE ATN AR SCREW 70MM STERILE ATN AR SCREW 75MM STERILE ATN AR SCREW 80MM STERILE ATN AR SCREW 85MM STERILE ATN AR SCREW 90MM STERILE ATN AR SCREW 95MM STERILE ATN AR SCREW 100MM STERILE…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1240-2018·2018-04-04
Zimmer Biomet Recalls Persona Partial Knee Spacer Blocks
Zimmer Biomet is recalling Persona Partial Knee Spacer Blocks because they may feel tight during trialing or appear loose in extension.
Product
Persona Partial Knee Spacer Blocks To assist in partial knee arthroplasty surgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1256-2018·2018-04-04
Encore Medical Recalls Altivate Anatomic Pegged Glenoid Trial Instruments
Encore Medical is recalling 92 units of Altivate Anatomic Pegged Glenoid Trials because the peg base design is larger on the trials than on the implants.
Product
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 38mm, REF 804-07-380 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.
Category
Medical Device
Distribution
Distributed nationwide