State

American Samoa product recalls

72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2251–2275 of 72944

HighFDA (Devices)·Z-1805-2026·2026-04-22
Philips AneurysmFlow MAFA ratio does not give reliable prognostic information
Philips is recalling AneurysmFlow because the Mean Aneurysm Flow Amplitude ratio does not reliably predict aneurysm occlusion after flow diverter stent treatment, yet is relied on clinically.
Product
Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to be used in combination with a Philips interventional X-ray system and 3DRA data.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0483-2026·2026-04-22
IMS epinephrine injection vials recalled over lack of sterility assurance
International Medication Systems is recalling one lot of Epinephrine Injection, USP, 1 mg/10 mL, citing lack of assurance of sterility. 81,520 units are affected.
Product
EPINEPHRINE — EPINEPHRINE (EPINEPHRINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1822-2026·2026-04-22
Cellex photopheresis kit centrifuge bowls may dislodge and break
Cellex Photopheresis Kits are being recalled because the centrifuge bowl is harder to install and, if fitted improperly, may dislodge and break during priming or treatment.
Product
Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software Version: Not Applicable Product Description: THERAKOS Photopheresis or extracorporeal photopheresis (ECP) is a photoimmune therapy where leukocytes are separa
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0455-2026·2026-04-22
SLMD benzoyl peroxide acne lotion recalled over benzene contamination
SLMD Benzoyl Peroxide Acne Lotion, 2.5% benzoyl peroxide, is being recalled because of chemical contamination from the presence of benzene. 2,500 bottles are affected.
Product
SLMD Benzoyl Peroxide Acne Lotion, Benzoyl Peroxide 2.5%, a) 0.7 fl. oz - 21 mL and b) 1.5 fl. oz. - 44mL bottles, SANDRA LEE MD., Distributed by Skin PS Brands, Culver City, CA 90232.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1812-2026·2026-04-22
Instinct Plus endoscopic clipping devices may malfunction during use
The Instinct Plus Endoscopic Clipping Device is being recalled after increased complaints indicating the device has the potential to malfunction. 713,702 units are affected.
Product
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1820-2026·2026-04-22
Cytal Burn Matrix 10x15 cm recalled over out-of-specification endotoxin results
Cytal Burn Matrix 10x15 cm dressings are being recalled because of an increased rate of out-of-specification endotoxin results. 226 units are affected.
Product
Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V259000·2026-04-22
Trails West RPM Freeride Recalled for Cooktop Flame Fire Risk
Trails West is recalling 2027 RPM Freeride recreational trailers because the cooktop flame may invert during furnace operation, increasing fire risk.
Product
TRAILS WEST — TRAILS WEST RPM FREERIDE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1818-2026·2026-04-22
Cytal Wound Matrix 10x15 cm recalled over out-of-specification endotoxin results
Cytal Wound Matrix 2-Layer 10x15 cm dressings are being recalled because of an increased rate of out-of-specification endotoxin results. 452 units are affected.
Product
Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1817-2026·2026-04-22
Cytal Wound Matrix recalled over out-of-specification endotoxin test results
Cytal Wound Matrix 2-Layer 7x10 cm dressings are being recalled because of an increased rate of out-of-specification endotoxin results. 46 units are affected.
Product
Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0449-2026·2026-04-22
Cipla cinacalcet 30 mg tablets exceed the nitrosamine daily intake limit
Cipla is recalling Cinacalcet Hydrochloride Tablets, 30 mg, over CGMP deviations and the presence of N-Nitroso Cinacalcet above the acceptable daily intake limit. 113,336 bottles are affected.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0530-2026·2026-04-22
Bupivacaine spinal ampules recalled nationwide over lack of sterility assurance
Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection, USP ampules are being recalled for lack of assurance of sterility. The action covers 3,260,170 ampules.
Product
BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0529-2026·2026-04-22
Huons lidocaine injection recalled nationwide over lack of sterility assurance
Lidocaine HCl Injection, USP 1% in 5 mL single dose vials manufactured by Huons is being recalled for lack of assurance of sterility. All lots within expiry are affected.
Product
LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0454-2026·2026-04-22
SLMD benzoyl peroxide spot treatment recalled over benzene contamination
SLMD BP Acne Spot Treatment, 10% benzoyl peroxide, is being recalled because of chemical contamination from the presence of benzene. 2,269 bottles are affected.
Product
SLMD BP Acne Spot Treatment, 10% Benzoyl Peroxide, 0.5 fl. oz - 15 mL bottles, Sandra Lee MD, Distributed by Skin PS Brands, Culver City, CA90232.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0487-2026·2026-04-22
Skin Script blemish spot treatment recalled for failing stability specifications
Skin Script Blemish Spot Treatment containing 1% salicylic acid is being recalled after it failed stability specifications. The action covers 28,163 bottles.
Product
Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873 9.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1824-2026·2026-04-22
Centurion circumcision kits distributed without the required sterilization process
Medline is recalling one lot of Centurion Circumcision Kits that was distributed without undergoing the required sterilization process and is therefore not sterile. 640 kits are affected.
Product
CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1821-2026·2026-04-22
Elegance anterior cervical plates recalled over burrs on finished product
Elegance Anterior Cervical Plates are being recalled over a quality issue involving the presence of burrs on the finished plate. The action covers 511 units.
Product
Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL PLATE, ELEGANCE 4 LEVEL CERVICAL PLATE Model/Catalog Number: See Excel sheet attached named "FDA 5072 Product Information" So
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1823-2026·2026-04-22
Gentuity HF-OCT imaging systems may repeat frames during catheter pullback
Gentuity is issuing a correction for HF-OCT Imaging Systems because frames may repeat during pullback with Vis-Rx catheters, affecting longitudinal length measurements.
Product
Gentuity HF-OCT Imaging System Model G10-01; Software version 23.2.13;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0451-2026·2026-04-22
Cipla cinacalcet 90 mg tablets exceed the nitrosamine daily intake limit
Cipla is recalling Cinacalcet Hydrochloride Tablets, 90 mg, over CGMP deviations and the presence of N-Nitroso Cinacalcet above the acceptable daily intake limit. 63,192 bottles are affected.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0452-2026·2026-04-22
FarmHouse Fresh benzoyl peroxide night lotion recalled over benzene contamination
FarmHouse Fresh Midnight Clearing Night Lotion, a 2.5% benzoyl peroxide acne treatment, is being recalled because of chemical contamination from the presence of benzene.
Product
FHF Farmhouse Fresh, Midnight Clearing, NIGHT LOTION, 2.5% BENZOYL PEROXIDE ACNE TREATMENT, OTC a) 0.5 fl. oz./15ml; and b)1 fl. oz./30ml tubes; Made in the USA for FarmHouse Fresh, 8797 CR 858 McKinney, Texas
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0488-2026·2026-04-22
Avantor magnesium chloride active pharmaceutical ingredient recalled as subpotent
Avantor Performance Materials is recalling one lot of bulk Magnesium Chloride 6-Hydrate active pharmaceutical ingredient because the material is subpotent. 36 bottles are affected.
Product
Magnesium Chloride, 6-Hydrate, Crystal, 500G per bottle, Bulk active pharmaceutical ingredient (API), Avantor Performance Materials, LLC, 100 Matsonford Road, Suite 200, Radnor, PA 19087, NDC 10106-2448-1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0475-2026·2026-04-22
Taro fluocinonide cream recalled for out-of-specification viscosity during stability testing
Taro is recalling one lot of Fluocinonide 0.05% Cream after stability testing returned out-of-specification viscosity results above the specification limit. 24,672 tubes are affected.
Product
FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0460-2026·2026-04-22
Discount Drug Mart menthol cough drops recalled after facility inspection findings
Discount Drug Mart Food Market Menthol Cough Suppressant Anesthetic Cough Drops, 30-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
DISCOUNT DRUG MART — DISCOUNT DRUG MART (COUGH DROPS MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0458-2026·2026-04-22
Caring Mill cherry cough drops recalled after facility inspection findings
Caring Mill Menthol Cough Suppressant Oral Anesthetic Cough Drops, cherry, 90-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
CARING MILL COUGH DROPS CHERRY — CARING MILL COUGH DROPS CHERRY (MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0466-2026·2026-04-22
Quality Choice sugar free honey lemon cough drops recalled after inspection findings
QC Quality Choice sugar free Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 25-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS HONEY LEMON SUGAR FREE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0456-2026·2026-04-22
Exchange Select honey lemon cough drops recalled after facility inspection findings
Exchange Select Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 30-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
HONEY LEMON FLAVOR COUGH DROP — HONEY LEMON FLAVOR COUGH DROP (HONEY LEMON FLAVOR COUGH DROP)
Category
Drug
Distribution
Distributed nationwide