State

American Samoa product recalls

73,366 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 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19351–19375 of 73391

ModerateFDA (Devices)·Z-1539-2022·2022-08-24
Poligrip Denture Adhesive Products Recalled for Improper Storage Conditions
Family Dollar Stores recalls multiple Poligrip denture adhesive products due to improper storage outside temperature-controlled areas. Affected products were sold between May 1 and June 10, 2022.
Product
POLIGRIP ADH CREAM FREE 2.4OZ, SKU 900334 POLIGRIP DENTURE ADHESIVE ORIGINAL 2.4OZ, SKU 900723 SUPER POLIGRIP ADH CREAM .75OZ, SKU 900085
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1349-2022·2022-08-24
Azacitidine for Injection Recalled Nationwide for Subpotent Dosage
Amerisource Health Services is recalling 4,160 vials of Azacitidine for Injection nationwide due to subpotency. The affected vials may contain less than the labeled 100 mg of active ingredient.
Product
Azacitidine for Injection, 100 mg Lyophilized Powder, Single-Dose Vials, Rx Only, Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213 India. Manufactured for BluePoint Laboratories. NDC 68001-0313-56
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1536-2022·2022-08-24
CURAD Waterproof Bandages Recalled for Improper Storage
Family Dollar is recalling CURAD waterproof bandages due to improper storage outside temperature-controlled conditions. The recall affects approximately 419 units sold nationwide between May 1 and June 10, 2022.
Product
CURAD STRNG WATRPRF STRIP 1IN 20CT, SKU
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1544-2022·2022-08-24
Polident Denture Cleansers Recalled Due to Improper Storage
Polident denture cleansers sold at Family Dollar stores nationwide are being recalled due to improper storage conditions. No illnesses or injuries have been reported.
Product
POLIDENT DENTURE CLEANSERS 84 CT, SKU 901634 POLIDENT DENTURE CLNS TAB 28CT, SKU 906131
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1527-2022·2022-08-24
VeriQuick Pregnancy Tests Recalled Due to Improper Storage
Family Dollar is recalling VeriQuick pregnancy tests that were not stored in temperature-controlled areas between April-June 2022. Improper storage conditions may affect test accuracy.
Product
VERIQUICK PREGNANCY TEST 1CT, SKU 901260, 939504
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1535-2022·2022-08-24
Travel Kit Toothbrush and Toothpaste Recalled Due to Improper Storage
Family Dollar is recalling approximately 1,555 travel kit toothbrush and toothpaste pouches that were stored in non-temperature-controlled areas. Products sold between May 1 and June 10, 2022 are affected.
Product
TRVL KIT TOTHBRSH CAP PASTE IN POUCH 1CT, SKU 900737
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1542-2022·2022-08-24
At-home marijuana test strips recalled for improper storage
Family Dollar is recalling at-home marijuana test strips (SKU 900752) that were stored outside temperature-controlled areas. Improper storage may affect test accuracy.
Product
AT HOME MARIJUANA TEST STRIP, SKU 900752
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1534-2022·2022-08-24
Denture Cleanser Tablets Recalled for Improper Storage Conditions
Family Dollar is recalling GS Denture Cleanser tablets (green and overnight formulas) due to improper storage in non-temperature-controlled areas. Products sold May 1 - June 10, 2022 may be affected.
Product
GS DENTURE CLEANSER GRN TAB 40CT, SKU 906312 GS DENTURE CLEAN OVRNT TAB 40CT, SKU 906023
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1547-2022·2022-08-24
KY Jelly Lubricant Recalled for Improper Storage Conditions
KY Jelly Lubricant 2 FL OZ (SKU 901443) distributed at Family Dollar stores was not stored in temperature-controlled areas. Consumers should discontinue use of product purchased between May–June 2022.
Product
KY JELLY LUBRICANT 2 FL OZ, SKU 901443
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1529-2022·2022-08-24
Temporary Dental Filling Product Recalled for Improper Storage
Family Dollar is recalling DENTEMP temporary dental filling products (SKU 902139) that were stored outside temperature-controlled conditions. The product was sold at Family Dollar stores nationwide between May and June 2022.
Product
DENTEMP ONE STEP .077OZ, SKU 902139
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22E071000·2022-08-23
Spyder Electronic Control Module Recall for Unintentional Awning Movement
Spyder Controls is recalling 1,047 Multiplex Electronic Control Modules because software defects may cause vehicle awnings to move unintentionally while parked.
Product
ELECTRICAL SYSTEM:SOFTWARE recall
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-08232022-01·2022-08-23
Perdue Frozen Gluten-Free Chicken Tenders Alerted for Foreign Material Contamination
USDA issued a public health alert for Perdue frozen gluten-free chicken tenders due to potential contamination with plastic and blue dye. No illnesses have been reported.
Product
Perdue Foods LLC — FSIS Issues Public Health Alert for Perdue Frozen Ready-To-Eat Chicken Tender Products Due to Foreign Material Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·22V636000·2022-08-23
Indian FTR 1200 S Motorcycles Recalled for Coolant Junction Leak Risk
Indian Motorcycle Company is recalling certain FTR 1200 and FTR 1200 S motorcycles due to a coolant junction that may leak, posing burn and crash risks to riders.
Product
INDIAN — INDIAN FTR 1200 S, FTR1200, FTR 1200 RALLY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E070000·2022-08-23
Firefly Recalls Multiplex Electronic Control Modules for Unintended Awning Movement
Firefly Integrations is recalling certain Multiplex Electronic Control Modules (ECM) because software defects may cause vehicle awnings to move unintentionally while parked, increasing the risk of injury.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V634000·2022-08-19
Thomas Built Buses Recalls Saf-T-Liner HDX School Buses for Seat Barrier Defect
Daimler Trucks North America is recalling 2011-2021 Thomas Built Saf-T-Liner HDX school buses because forward seat barriers may not provide sufficient protection, increasing injury risk in crashes.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V635000·2022-08-19
Indian Motorcycle Recalls 28,689 Models for Electrical Connection Failure
Indian Motorcycle is recalling 28,689 motorcycles from 2014-2020 because a failing electrical connection may cause loss of front lights, increasing crash risk.
Product
INDIAN — INDIAN CHIEFTAIN DARK HORSE, CHIEFTAIN, CHIEF VINTAGE, SPRINGFIELD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V633000·2022-08-18
2020-2022 Hyundai Palisade vehicles recalled for tow hitch fire
Hyundai is recalling 2020-2022 Palisade vehicles with tow hitch harnesses that may accumulate debris and moisture, causing electrical shorts and fire risk. Dealers will install replacement fuses and wire kits.
Product
HYUNDAI — HYUNDAI PALISADE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22201·2022-08-18
ASUS ROG Maximus Z690 Hero Motherboards Recalled for Fire and Burn Hazards
ASUS Computer International is recalling about 10,000 ASUS ROG Maximus Z690 Hero motherboards because a capacitor installed in reverse position can cause short circuits, overheating, or melting. ASUS has received 10 reports of overheating and melting, though no injuries have been reported.
Product
ASUS ROG Maximus Z690 Hero Motherboards
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·22202·2022-08-18
Hard Rock Cafe Children's Hooded Sweatshirts Recalled for Strangulation Hazard
Hard Rock Cafe is recalling about 1,550 children's hooded sweatshirts with drawstrings in the hood that can become entangled or caught on objects, posing a strangulation hazard to children. No injuries have been reported.
Product
Hard Rock Cafe Children's Hooded Sweatshirts
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V632000·2022-08-18
2022-2023 Hyundai Elantra Airbag Emblem Detachment Safety Recall
Hyundai is recalling certain 2022-2023 Elantra vehicles due to an improperly welded driver's airbag cover emblem that may detach during deployment and strike occupants, increasing injury risk.
Product
HYUNDAI — HYUNDAI ELANTRA N, ELANTRA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1398-2022·2022-08-17
FDA Recalls Viral Transport Containers Distributed Without Clearance
FDA recalls approximately 8.7 million viral transport containers that were distributed without regulatory clearance and without complying with FDA guidance for proper viral transport specifications.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1399-2022·2022-08-17
FDA Recalls 3.95 Million Viral Transport Containers Distributed Without Clearance
The FDA recalled 3.95 million viral transport containers distributed without FDA clearance and in violation of established guidance. The containers were distributed worldwide, including to facilities in California, Florida, Illinois, and New York.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1400-2022·2022-08-17
Viral Transport Container Distributed Without FDA Clearance or Guidance Compliance
Haimen Shengbang Laboratory Equipment recalled 100,000 viral transport containers distributed without FDA clearance and outside FDA guidance, affecting facilities in California, Florida, Illinois, New York, and China.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22E069000·2022-08-17
S&B Diesel Fuel Tank Recall for Insufficient Driveline Clearance
S&B Filters is recalling certain diesel fuel tanks for RAM Mega Cab vehicles due to insufficient clearance that may cause fuel leaks and fire risk.
Product
FUEL SYSTEM, DIESEL:STORAGE:TANK ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1311-2022·2022-08-17
Triple Antibiotic Ointment Recalled Due to Improper Storage
McKesson Medical-Surgical Inc. is recalling Triple Antibiotic Ointment due to storage deviations that violated drug label specifications and current good manufacturing practices.
Product
Triple Antibiotic Ointment, Bacitracin zinc, Neomycin sulfate, Polymixin B sulfate, First Aid Antibiotic, Triple Antibiotic Ointment, 144 packets per box, Net wt. per packet 0.5 g, Honeywell Safety Products, NDC 0498-0750-36.
Category
Drug
Distribution
Distributed nationwide