State

American Samoa product recalls

73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21451–21475 of 73413

SevereFDA (Food)·F-0919-2022·2022-03-16
Abbott Similac Human Milk Fortifier Recalled Due to Pathogen Risk
Abbott Similac Human Milk Fortifier pouches are recalled due to potential Cronobacter sakazakii and Salmonella Newport contamination. The recall affects infants who may have received contaminated product.
Product
Abbott Similac Human Milk Fortifier 0.9g Pouch / Sachet, 50 Pouch / Sachet per retail unit. 3 retail units per case Item numbers: 54598 5459813 5459814 5459820 5459886 6771009 Retail UPCs: 70074545998 070074545998 055325545996 070074109404 070074103297…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0717-2022·2022-03-16
Luscient Diagnostics COVID-19 Antigen Test Kits Recalled for Lack of FDA Authorization
Lusys Laboratories' Luscient Diagnostics COVID-19 Antigen Test Kits are being recalled because they lack FDA authorization. The kits were not approved, cleared, or authorized for distribution in the United States.
Product
Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Nasal Swab Test)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0943-2022·2022-03-16
Abbott Similac 360 Infant Formula recalled for Cronobacter and Salmonella
Abbott is recalling Similac 360 Total Care Infant Formula due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants, with Cronobacter found in the manufacturing facility.
Product
Abbott Similac 360 Total Care Infant Formula with Iron 20.6oz. and 30.3oz. palstic jar. 4 jars per case. 7oz. can. 6 cans per case. Item numbers: 68063 68065 68109 Retail UPCs: 070074680644 070074680668 070074681108
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0955-2022·2022-03-16
Abbott Similac Alimentum Infant Formula Recalled for Cronobacter and Salmonella Contamination
Abbott Laboratories is recalling 45,223 cases of Similac Alimentum infant formula due to consumer complaints involving Cronobacter sakazakii and Salmonella Newport in infants, and evidence of Cronobacter sakazakii in the manufacturing facility.
Product
Abbott Similac Alimentum Allergies & Colic Hypoallergenic Infant Formula 400g. can. 6 cans per case. Item numbers: 5707713 Retail UPCs: 055325000624
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0929-2022·2022-03-16
Abbott Similac EleCare infant formula recalled for pathogen contamination
Abbott is recalling approximately 95,077 cases of Similac EleCare infant formula due to consumer complaints involving Cronobacter sakazakii and Salmonella Newport in infants, and detection of Cronobacter sakazakii in the manufacturing facility.
Product
Abbott Similac EleCare HMO, Abbott Similac EleCare, Abbott EleCare Similac Gold, Abbott EleCare Similac 400g can. 6 cans per case Item numbers: 6676006 6676012 6676021 6676025 6676030 6676045 6676053 6676057 Retail UPCs: 8699548995217 0070074124155…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0947-2022·2022-03-16
Abbott Similac 360 Infant Formula Recalled for Cronobacter and Salmonella Contamination
Abbott Laboratories is recalling Similac 360 Total Care Sensitive Infant Formula due to potential Cronobacter sakazakii or Salmonella Newport contamination. The recall affects products distributed in the United States and worldwide.
Product
Abbott Similac 360 Total Care Sensitive Infant Formula with Iron 7oz. can. 6 cans per case. 20.1oz. and 29.5oz. plastic jar. 4 jars per case. Item numbers: 68070 68072 68118 Retail UPCs: 070074680712 070074680736 070074681191
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0926-2022·2022-03-16
Abbott Similac Sensitive Infant Formula Recalled for Bacterial Contamination
Abbott Similac Sensitive infant formula is being recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants, with evidence of bacterial contamination in the manufacturing facility.
Product
Abbott Similac Sensitive Lactose Sensitivity 22oz. plastic jar. 6 jars per case. Item numbers: 6499813 Retail UPCs: 055325001218
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0694-2022·2022-03-16
Medtronic TurboHawk Plus Directional Atherectomy System Recalled Due to Design Defect
ev3 Inc. is recalling the Medtronic TurboHawk Plus Directional Atherectomy System due to design similarities to a device with reported tip detachment and embolization incidents. The FDA has classified this as a Class I recall.
Product
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Multi-vessel, Catalog number THP-M. For use in peripheral vasculature.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0695-2022·2022-03-16
Medtronic TurboHawk Plus atherectomy system recalled for potential tip detachment
The Medtronic TurboHawk Plus Directional Atherectomy System (catalog THP-S) is being recalled due to design similarities to another device that experienced tip detachment and embolization. The recall affects 245 devices distributed nationwide.
Product
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number THP-S. For use in peripheral vasculature.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V163000·2022-03-16
2022 Volkswagen Golf R engine design cover fire risk recall
The engine design cover in 2022 Volkswagen Golf R vehicles may loosen during high acceleration and contact hot engine surfaces, increasing fire risk. Dealers will remove it free of charge.
Product
VOLKSWAGEN — VOLKSWAGEN GOLF R, GTI
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0741-2022·2022-03-16
FISH Diagnostic Probe Kit Color Labeling Error Affects Test Results
Cytocell Ltd. is recalling a Del(5q) Deletion FISH Probe Kit due to incorrect color labeling on probe components. The mislabeling may cause misinterpretation of test results for patients with AML or MDS.
Product
Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Number: USA-LPH024
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0727-2022·2022-03-16
B. Braun dispensing pins recalled for air filter leakage risk
B. Braun Medical is recalling dispensing pins with an elevated leakage risk in the air inlet filter. The leakage may reduce medication doses, delay treatment, or contaminate the fluid path, potentially causing bloodstream infection.
Product
Dispensing Pins for Air Inlet Filter, Product Catalog No. 412005, DP2500 Dispensing Pin W/Valve. A valve for aspiration or injection of medication or enteral feeding solution from inverted multi-dose vials.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0743-2022·2022-03-16
Medtronic endotracheal tubes recalled due to manufacturing nonconformity
Medtronic Xomed is recalling over 301,000 NIM TRIVANTAGE EMG Endotracheal Tubes due to a manufacturing nonconformity. These devices were distributed worldwide.
Product
NIM TRIVANTAGE EMG Endotracheal Tube
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0725-2022·2022-03-16
Philips X-ray System Cooling Leak Poses Fire Risk
Philips Allura CV20 X-ray systems with certain Laird chillers may leak cooling liquid onto electrical components, potentially causing fire or smoke. Affected systems should not be operated until the issue is addressed.
Product
Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0732-2022·2022-03-16
Radiation therapy planning software displays wrong images during animation playback
RayStation/RayPlan versions 6.0.0.24 through 9.2.0.483 incorrectly display selected images as both primary and secondary when animation playback is running, affecting treatment planning visualization.
Product
RayStation/RayPlan- designed for treatment planning and analysis of radiation therapy. Software Version: 6.0.0.24 , 6.1.0.26 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 .…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0724-2022·2022-03-16
Philips Allura Xper X-ray systems cooling system leak poses fire risk
Philips Allura Xper interventional X-ray systems may experience cooling liquid leaks that could drip on electrical components, creating risk of fire, smoke, or burning odors. No injuries have been reported.
Product
Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an extended drip tray: Model Number: 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0738-2022·2022-03-16
FDA Recalls Diagnostic Test Strips for False Positive Results
NeuMoDx COVID-19 test strips (Lot 116305 S/L-02) are recalled due to product contamination that increases risk of false positive results. The recall affects 102 boxes distributed in FL, MD, MI, and NY.
Product
NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip, Ref # 300900 (marketed under EUA202947). Distributed in boxes of 6 assay strips in individual pouches. Box, pouch and strips all labeled with product name, ref #, lot #, and expiration date.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0739-2022·2022-03-16
Nextra CH Hammertoe Surgical Implant Kit Recalled for Locking Mechanism Defect
Nextremity Solutions recalls the Nextra CH Hammertoe Mini Instrument Kit for a defect that may deform the implant's locking mechanism during insertion, potentially requiring revision surgery.
Product
Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes SKU: CH-MINI-KT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0729-2022·2022-03-16
Vascular Graft Mislabeled; Packaging Labels Do Not Match Product Specifications
A vascular graft has been recalled due to labeling mismatch: the outer package label differs from the inner sterile packaging in graft type and dimensions. Implanting the wrong size could disrupt blood vessel connections and create a pseudo-aneurysm.
Product
HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M002020952070
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22103·2022-03-16
B. toys Wooden Activity Walker recalled for choking hazard
B. toys Walk 'n' Learn wooden toddler walkers are being recalled because wheels and attachment hardware can detach in small pieces, creating a choking hazard for young children. Battat has received six reports of detachment, including one incident where a child placed a detached metal nut in her mouth.
Product
B. toys Wooden Activity Walker - Walk 'n' Learn
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V162000·2022-03-16
2021 Volkswagen ID.4 Battery Cell Soldering Defect Recall
Volkswagen is recalling certain 2021 ID.4 vehicles due to improper soldering of the high-voltage battery connection. The defect may cause an unreliable connection that could lead to vehicle stalling and increase crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0823-2022·2022-03-16
El Chavito Saladitos Enchilados Salted Plums Recalled for Potential Lead Contamination
El Chavito Saladitos Enchilados Salted Plums (1.7 oz.) are being recalled nationwide due to potential lead contamination. Consumers should not consume this product.
Product
El Chavito¿ Saladitos Enchilados Salted Plums with Chili, net wt. 1.7 oz., Individual UPC 859470006070, Master Case UPC 859470006612.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0740-2022·2022-03-16
Surgical hammertoe instruments recalled for potential locking mechanism deformation
The Nextra Cannulated Hammertoe Standard Instrument Kit's driver may deform the implant locking mechanism during insertion, potentially requiring revision surgery.
Product
Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe SKU: CH-STD-KT
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22099·2022-03-16
Reckitt Recalls 3.74 Million Bottles of Airborne Gummies for Pressure Hazard
RB Health (Reckitt) is recalling approximately 3.74 million bottles of Airborne Gummies (63 and 75 count) because pressure buildup can cause the cap and seal to pop off with force upon first opening, posing an injury hazard.
Product
Airborne Gummies (63 and 75 count bottles)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0735-2022·2022-03-16
Laboratory diagnostic tips recalled for potential dispensing errors
Ortho-Clinical Diagnostics is recalling VITROS Chemistry VersaTips due to shape deformity that may reduce sample volume by 16%. Undetected errors could result in inaccurate test results for bloodborne infectious disease assays.
Product
VITROS Chemistry Products VersaTips, Catalog No. 6801715 A VersaTip sales unit is composed of 1000 tips per box.
Category
Medical Device
Distribution
Distributed nationwide