State

American Samoa product recalls

73,495 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 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24376–24400 of 73520

HighFDA (Devices)·Z-1950-2021·2021-06-30
Econocare Plus Waffle Overlay Recalled for Bodily Fluid Contamination
EHOB, Inc. is recalling 70 units of the Econocare Plus Waffle Overlay due to trace amounts of dried bodily fluids that may expose patients and healthcare providers to contaminants.
Product
Econocare Plus Waffle Overlay- Intended for use as a medical device to aid in the prevention and treatment of pressure injuries or bed sores and general comfort. Product Code: 1025ECP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1941-2021·2021-06-30
OptiChamber Diamond Spacer Recalled Due to Temperature Exposure During Shipping
Cardinal Health is recalling 375 OptiChamber Diamond Spacer devices due to temperature exposure during shipping that may cause inaccurate medication delivery results. Affected devices were distributed to Florida, Georgia, and South Carolina.
Product
OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0640-2021·2021-06-30
Metformin Hydrochloride Tablets Recalled for NDMA Contamination
Viona Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg due to detection of N-Nitrosodimethylamine (NDMA) levels exceeding acceptable daily intake limits.
Product
METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1951-2021·2021-06-30
LEGION Knee Prosthesis Component Recalled for Manufacturing Surface Damage
Smith & Nephew is recalling 5 units of a knee prosthesis component due to surface damage from a manufacturing error. The affected lot was distributed in specific U.S. states.
Product
LEGION Posterior Stabilized OXINIUM Femoral Component, REF 71421216, Size 6, Left, Nonporous Femoral Component, A/P 65.5 MM, M/L 73 MM, For Cemented Use Only, ZR-2.5NB,Sterile. Knee prosthesis component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1936-2021·2021-06-30
OneTouch Ultra Blue test strips recalled for temperature exposure damage
Cardinal Health is recalling 5,356 boxes of OneTouch Ultra Blue test strips after units were exposed to freezing temperatures during shipping, which may cause inaccurate glucose readings.
Product
ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1927-2021·2021-06-30
Cardiac assessment system may display test reports in wrong patient records
GE Healthcare's Case Cardiac Assessment System and CardioSoft diagnostic application may display one patient's cardiac test report in another patient's medical record under certain conditions. No patient injuries have been reported.
Product
Case Cardiac Assessment System for Exercise Testing and CardioSoft Diagnostic System Exercise Stress Testing ECG application
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0686-2021·2021-06-30
Clio Vanilla Greek Yogurt Mini Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Vanilla Greek Yogurt Mini Bars due to the possibility of metal fragments in the product. Consumers should not consume affected yogurt bars.
Product
Clio Vanilla Greek Yogurt Mini Bars wrapped in a Chocolate Coating 6.2oz pouch x 6 pouches per case, UPC: 854021008077
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1932-2021·2021-06-30
AeroChamber PLS Spacer Recalled Due to Temperature Exposure During Shipping
Cardinal Health is recalling AeroChamber PLS spacers exposed to freezing temperatures during shipping, which may cause inaccurate drug delivery results. Affected units shipped between February and March 2021 in Florida, Georgia, and South Carolina.
Product
AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0693-2021·2021-06-30
Clio Peach Less Sugar Yogurt Bars recalled for possible metal fragments
Clio LLC is recalling Clio Peach Less Sugar Yogurt Bars due to the possible presence of metal fragments in the product. The 10-pack boxes with best buy dates between 2/7/2021 and 6/20/2021 were distributed nationwide.
Product
Clio Peach Less Sugar Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 854021008213
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0690-2021·2021-06-30
Clio Honey Greek Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Honey Greek Yogurt Bars due to the possibility of metal fragments in the product. The recall affects 5,423 cases distributed nationwide with best-by dates between March 7, 2021 and July 11, 2021.
Product
Clio Honey Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 861703000168
Category
Food
Distribution
Distributed nationwide
HighNHTSA·21V492000·2021-06-30
2021 Volkswagen Jetta Air Bag Control Module Welding Defect Recall
Volkswagen is recalling 2020-2021 Jetta vehicles because the air bag control module was welded in an incorrect position. This can cause air bags to deploy improperly during a crash or deploy unexpectedly, increasing injury risk.
Product
VOLKSWAGEN — VOLKSWAGEN JETTA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0697-2021·2021-06-30
Clio Greek Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Vanilla and Strawberry Club pack Greek Yogurt Bars nationwide due to the possibility of metal fragments in the product. Consumers should not eat the affected bars.
Product
Clio Vanilla / Strawberry Club pack Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 12 , 16pc tray, 24g x 24 (12pc tray), 55g x 16 (8pc tray). UPC codes: 854021008121, 854021008138, and 854021008022
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0692-2021·2021-06-30
Clio Mixed Berry Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Mixed Berry Less Sugar Yogurt Bars due to possible metal fragments in the product. Consumers should not eat the affected bars and should contact the company or return them to the retailer.
Product
Clio Mixed Berry Less Sugar Yogurt Bars wrapped in a Chocolate Coating 10 Clio Retail 10-pack, UPC code: 854021008190
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1937-2021·2021-06-30
OneTouch Ultrasoft Lancets recalled due to temperature exposure during shipping
Cardinal Health is recalling 531 boxes of OneTouch Ultrasoft Lancets shipped February-March 2021 due to temperature exposure during shipment that may cause inaccurate test results.
Product
ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21157·2021-06-30
Children's Nightgowns Recalled for Flammability Standard Violation
About 4,900 Booph children's nightgowns sold on Amazon from March through June 2021 are being recalled because they fail to meet federal flammability standards for sleepwear, posing a burn risk to children.
Product
Children's Nightgowns
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0638-2021·2021-06-30
Mephyton Phytonadione 5 mg Tablets Recall for Failed Impurity Specifications
Bausch Health Companies is recalling Mephyton (Phytonadione) 5 mg tablets nationwide because certain lots failed impurities and degradation specifications. Affected consumers should contact their healthcare provider.
Product
Mephyton (Phytonadione) 5 mg tablets, 100-count tablets, Rx Only, Manufactured for: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ, 08807, USA, NDC 0187-1704-05.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0702-2021·2021-06-30
Favorite Day Caramel Cashew Trail Mix Recalled for Plastic Contamination
John B. Sanfilippo & Son Inc. is recalling Favorite Day Caramel Cashew Trail Mix nationwide because the product may contain stringy pieces of flexible plastic.
Product
favorite day caramel cashew Trail Mix, Product Number 04312. Milk Chocolate caramel balls, cashews, M&M'S milk chocolate candies and Peanuts. Net Wt 14 oz. (396g), UPC 85239-15671
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1945-2021·2021-06-30
Medical Action Industries Hemostats Recalled for Flaking Metal Defects
Medical Action Industries is recalling Mosquito Hemostats due to potential flaking metal and brown spots on the devices. The recall affects 23 boxes of surgical instruments distributed nationwide.
Product
Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1942-2021·2021-06-30
Blood Glucose Test Strips Recalled for Temperature Exposure During Shipping
Cardinal Health is recalling ACCU-CHEK SMARTVIEW 100 test strips distributed in Florida, Georgia, and South Carolina due to temperature excursions during shipping that may cause inaccurate glucose readings.
Product
ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0636-2021·2021-06-30
Diflorasone Diacetate Ointment recalled for foreign particles
Teligent Pharma is recalling Diflorasone Diacetate Ointment USP 0.05% due to the presence of foreign particles found during routine stability testing. The recall affects 6,240 tubes distributed nationwide.
Product
Diflorasone Diacetate Ointment USP, 0.05%, packaged in a)15 g (NDC 52565-063-15) and b) 30 g (NDC 52565-063-30) tubes, Rx only, Manufactured by: Teligent Pharma, Inc, Buena, NJ 08310.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0701-2021·2021-06-30
Favorite Day Peanut Butter Chocolate Trail Mix Recalled for Plastic Pieces
John B. Sanfilippo & Son Inc. is recalling Favorite Day Peanut Butter Chocolate Trail Mix because some packages may contain stringy pieces of flexible plastic.
Product
favorite day peanut butter chocolate Trail Mix, Product Number 04315. Peanut butter cups, Milk Chocolate-covered cereal squares, peanuts, chocolate chips and Peanut Butter Chips. Net Wt 8 oz. (226g), UPC 85239-15683
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1935-2021·2021-06-30
Vicks vaporizers recalled for temperature exposure during shipping
Cardinal Health is recalling Vicks 1.5-gallon vaporizers exposed to temperature excursions during shipping delays in February-March 2021, which may cause inaccurate results. Affected units were distributed in Florida, Georgia, and South Carolina.
Product
VAPORIZER VICKS 1.5GAL Item Number: 2354942
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1943-2021·2021-06-30
LED therapy device pads recalled for improper cord assembly and power failure risk
Inlightened Partners LLC is recalling 926 inLight Medical LED Pads due to improper assembly of cord connectors, which may cause power interruptions and controller shutdown.
Product
inLight Medical LED Pads used with Polychromatic light technology system
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0639-2021·2021-06-30
Phytonadione 5 mg Tablets Recalled for Failed Impurity Specifications
Bausch Health Companies is recalling Phytonadione 5 mg tablets distributed nationwide because the affected lots failed to meet impurity and degradation specifications. Consumers should consult their healthcare provider before stopping this medication.
Product
Phytonadione Tablets, 5 mg, 30-count ablets, Rx only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA, NDC 68682-170-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V489000·2021-06-29
East Manufacturing Recalls 2018-2021 MMX Trailers for Steering Defect
East Manufacturing is recalling 2018-2021 MMX trailers because the steering arm may detach, potentially causing loss of steering control and increasing crash risk.
Product
EAST MANUFACTURING — EAST MANUFACTURING MMX
Category
Vehicle
Distribution
Distributed nationwide