State

American Samoa product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44476–44500 of 73842

HighFDA (Devices)·Z-1124-2017·2017-02-08
Synthes Radial Head Prosthesis Recalled for Potential Stem Loosening
Synthes (USA) Products LLC is recalling 50,311 units of the Radial Head Prosthesis System because the radial stem may loosen post-operatively at the stem bone interface.
Product
Synthes Radial Head Prosthesis System, Surgical instrument motors and accessories Product Usage: Intended for primary and revision joint replacement of the radial head.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1135-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising product sterility.
Product
Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1111-2017·2017-02-08
Organ Preservation Solution Recalled for Potential Bacterial Contamination
Organ Recovery Systems is recalling SPS-1 Static Preservation Solution bags due to potential bacterial contamination.
Product
SPS-1, Static Preservation Solution [1 or 2 liter bags], Sterile; Organ Recovery Systems, One Pierce Place, Itasca, IL 60143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0450-2017·2017-02-08
Dr. Reddy's Recalls Flucanazole Tablets for Dissolution Failures
Dr. Reddy's is recalling Flucanazole tablets that failed dissolution and stability specifications. Patients should stop using the affected lots and consult their healthcare provider.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1121-2017·2017-02-08
Medtronic Strata II Valves Recalled for Pressure Discrepancies
Medtronic is recalling Strata II and Strata NSC valves used for hydrocephalus management due to reported discrepancies between the set pressure level and x-ray readings.
Product
Medtronic Strata II / Strata NSC Valves (includes Burr Hole and Lumbar Peritoneal. All Catalog Numbers. Strata-type valves are used in the management of hydrocephalus. The Strata II/Strata NSC valve is a shunt component designed to allow for continuous flow of cerebrospinal…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·17083·2017-02-08
La-Z-Boy Recalls Lift Chair Power Supplies Due to Shock Hazard
La-Z-Boy is recalling specific power supplies sold with lift chairs because the covers can crack and detach, exposing electrical components and posing a shock hazard.
Product
Power supplies sold with lift chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1120-2017·2017-02-08
Siemens IMMULITE PSA Kit Recall Due to Negative Bias Results
Siemens is recalling two lots of IMMULITE PSA kits because they produce negative bias results, potentially affecting prostate cancer screening accuracy.
Product
IMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LK3PS1, SMN 10706293 (US Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers for the quantitative measurement of prostate-specific antigen (PSA) in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1125-2017·2017-02-08
Covidien Nellcor SpO2 Forehead Sensor Recalled for Latex Labeling Error
FDA is recalling 7,453 units of the Covidien Nellcor SpO2 Forehead Sensor because the label incorrectly states the product is latex-free, while the headband contains latex.
Product
Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10; The Covidien Nellcor¿ Forehead SpO2Sensor, model RS10, is indicated for use when continuous non-invasive arterial oxygen saturation and pulse rate monitoring are required for patients weighing more than 40 kg.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1129-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling 252 Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The devices are used for breast tissue removal.
Product
Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0465-2017·2017-02-08
VistaPharm Recalls Methadone Hydrochloride Due to Potential Bacterial Contamination
VistaPharm is recalling Methadone Hydrochloride Oral Concentrate because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Product
METHADONE HYDROCHLORIDE — METHADONE HYDROCHLORIDE (METHADONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·17V078000·2017-02-08
Mercedes-Benz Recalls 2017 E300 Models Due to Shift Lever Module Defect
Mercedes-Benz is recalling 2017 E300 and E300 4Matic vehicles because a damaged shift lever module may prevent gear selection, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ E300
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1134-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling 326 Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers units distributed in the US and several international countries.
Product
Intact Disposable Wands (part of the Intact System) 777-120: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1119-2017·2017-02-08
Siemens Recalls IMMULITE PSA Kits Due to Negative Bias
Siemens Healthcare Diagnostics is recalling IMMULITE PSA kits worldwide because patient samples show an average negative bias of approximately -22%.
Product
IMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LKUP1, SMN 10380956 (OUS Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers for the quantitative measurement of prostate-specific antigen (PSA) in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1130-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling 185 units of Intact Disposable Wands because the sterile barrier was breached, compromising sterility.
Product
Intact Disposable Wands (part of the Intact System) 900-115: 5 Pack 15mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1131-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers 320 units distributed worldwide.
Product
Intact Disposable Wands (part of the Intact System) 777-115: 5 Pack 15mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0452-2017·2017-02-08
Dr. Reddy's Recalls Flucanazole Tablets for Dissolution Failures
Dr. Reddy's Laboratories is recalling Flucanazole 200 mg tablets nationwide due to failed dissolution specifications and stability issues.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0451-2017·2017-02-08
Dr. Reddy's Recalls Flucanazole Tablets Due to Dissolution Failures
Dr. Reddy's Laboratories is recalling Flucanazole 150 mg tablets because they failed dissolution specifications and 18-month stability testing.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1109-2017·2017-02-08
Immuno-Mycologics Recalls Cryptococcal Antigen Lateral Flow Assay Due to False Positives
Immuno-Mycologics is recalling 630 units of the Cryptococcal Antigen Lateral Flow Assay because specific lots have lower specificity, leading to reported false positive results.
Product
Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Reference # CR2003
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1115-2017·2017-02-08
Zimmer Biomet Recalls Vanguard Total Knee System Femoral Components Due to Labeling Errors
Zimmer Biomet is recalling Vanguard Total Knee System femoral components because packaging labels may incorrectly identify the size or side of the implant.
Product
Vanguard Total Knee System Vanguard Open Box Femoral Components Item Number: 183100 Description: VNGD PS OPEN INTL FEM RT 55 Item Number: 183102 Description: VNGD PS OPEN INTL FEM-RT 57.5 Item Number: 183104 Description: VNGD PS OPEN INTL FEM RT 60 Item Number: 183106…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1117-2017·2017-02-08
Ortho-Clinical VITROS Na+ Slides Recalled for Potential Biased Results
Ortho-Clinical Diagnostics is recalling VITROS Na+ Slides because they may produce biased results if stored on the analyzer for 10 days after minimum warm-up.
Product
VITROS Na+ Slides, (UPN 10758750004812) For in vitro diagnostic use only. VITROS Na+ Slides quantitatively measure sodium (Na+) concentration in serum, plasma, and urine using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1118-2017·2017-02-08
Siemens Mammomat Inspiration Mammography Systems Recalled for Software Error
Siemens Medical Solutions USA is recalling 55 Mammomat Inspiration digital x-ray mammography systems due to a software error.
Product
Mammomat Inspiration full, field digital,system,x-ray,mammographic Product Usage: The Mammomat Inspiration system is intended for mammography exams, screening, diagnosis, and stereotactic biopsies under the supervision of medical professionals. Mammographic images can be…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1427-2017·2017-02-08
Roland Manzanilla Olives Stuffed With Anchovies Recalled for Microorganisms
Roland Foods is recalling Manzanilla Olives Stuffed With Anchovies because FDA sampling found non-pathogenic Gram Positive Rods.
Product
Roland MANZANILLA OLIVES STUFFED WITH ANCHOVIES, DR. WT. 3 OZ. (85g), UPC Code: 41224714021 and Case UPC Code: 10041224714028, Item # 71402, PRODUCT OF SPAIN
Category
Food
Distribution
Distributed nationwide
HighCPSC·17732·2017-02-07
Sony Expands Recall of VAIO Laptop Battery Packs for Fire Hazards
Sony is expanding a recall of Panasonic lithium-ion battery packs used in VAIO laptops due to overheating risks that can cause burns and fires.
Product
Panasonic battery packs used in Sony Electronics laptop computers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·17V074000·2017-02-07
Cruiser RV Recalls 2016-2017 Boss Trailers Due to Furnace Exhaust Defect
Cruiser RV is recalling 2016-2017 Boss recreational trailers because a vertically-mounted furnace may have exhaust ports at the top, creating an unsafe operating condition.
Product
CRUISER RV — CRUISER RV BOSS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V073000·2017-02-03
Lamborghini Recalls 2012-2017 Aventador Models Due to Fuel Leak Fire Risk
Lamborghini is recalling 2012-2017 Aventador vehicles because gasoline may contact the exhaust system, increasing the risk of a fire.
Product
LAMBORGHINI — LAMBORGHINI AVENTADOR
Category
Vehicle
Distribution
Distributed nationwide