State

American Samoa product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46751–46775 of 73849

SevereFDA (Devices)·Z-2677-2016·2016-09-07
Intuitive Surgical Recalls da Vinci EndoWrist Stapler 30 Instruments
Intuitive Surgical is recalling 875 da Vinci EndoWrist Stapler 30 instruments due to reported shaft rotation interruptions and jaw opening failures.
Product
CURVED-TIP STAPLER 30,IS4000; Model number 470530; General and Plastic Surgery: The Intuitive Surgical da Vinci EndoWrist Stapler 30 Instrument and Stapler 30 Reloads are intended to be used with the da Vinci Xi Surgical System (Model IS4000) for resection, transection…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V647000·2016-09-07
Volkswagen and Audi Recall 2015-2016 Models for Fuel Leak Fire Risk
Volkswagen is recalling 2015-2016 Golf, GTI, and Audi A3 vehicles because a faulty fuel pump may cause leaks that increase fire risk.
Product
VOLKSWAGEN — VOLKSWAGEN, AUDI GOLF, GTI, A3 CABRIOLET
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-2016-2016·2016-09-07
Hampton Creek Muffin Mix Recalled for Salmonella in Coconut Milk Powder
Hampton Creek Foods is recalling JUST Chocolate Chunk Muffin Mix because a positive test result for Salmonella was found in the coconut milk powder used in manufacturing.
Product
JUST Chocolate Chunk Muffin Mix; NET WT 20.8 oz. (1 lb 4.8 oz) 590 g); UPC 8 54829 00656 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2018-2016·2016-09-07
Hampton Creek Blueberry Muffin Mix Recalled for Salmonella Risk
Hampton Creek Foods is recalling JUST Blueberry Muffin Mix because a positive test for Salmonella was found in the coconut milk powder used to make it.
Product
JUST Blueberry Muffin Mix; NET WT 23.3 oz. (1 lb 7.3 oz) 660 g); UPC 8 54829 00685 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2035-2016·2016-09-07
Hampton Creek Cinnamon Roll Coffee Cake Mix Recalled for Salmonella
Hampton Creek Foods is recalling JUST Cinnamon Roll Coffee Cake Mix because a positive test for Salmonella was found in the coconut milk powder used in its manufacturing.
Product
JUST Cinnamon Roll Coffee Cake Mix; NET WT 26.9 oz. (1 lb 10.9 oz) 762 g); UPC 8 54829 00644 2. Ingredients: Cake Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2019-2016·2016-09-07
Hampton Creek Devil's Food Cake Mix Recalled for Salmonella
Hampton Creek Foods is recalling Devil's Food Cake Mix because a positive test found Salmonella in the coconut milk powder used in manufacturing.
Product
JUST Devil's Food Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC 8 54829 00643 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2017-2016·2016-09-07
Hampton Creek Recalls JUST Yellow Cake Mix Due to Salmonella Risk
Hampton Creek Foods is recalling JUST Yellow Cake Mix because a positive test for Salmonella was found in the coconut milk powder used to make it.
Product
JUST Yellow Cake Mix; NET WT 20 z. (1 lb 4oz) 567 g); UPC 8 54829 00642 8. Ingredients: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin, reduced Iron…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2692-2016·2016-09-07
Beckman Coulter Recalls UniCel DxH Slidemaker Stainer Due to Fire Risk
Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer because flammable liquids may contact electrical components, posing a fire hazard.
Product
UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Catalog No. 775222 UniCel DxH Slidemaker Stainer (DxH SMS) Instructions for Use (IFU) Part Number B26647AC The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-2008-2016·2016-09-07
IFS Raw Shelled Pistachios Recalled for Potential Salmonella Contamination
International Foodsource LLC is recalling raw shelled pistachios due to potential Salmonella contamination found in FDA testing.
Product
IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. 3 lb. (1 kg) International Foodsource LLC 52 Richboynton Rd. Dover NJ 07801 UPC 790429243026
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2673-2016·2016-09-07
Nakanishi Diamond Coated Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 2,574 diamond coated tips and burs because the labeling failed to indicate they are single-use only, posing a cross-contamination risk.
Product
Diamond Coated Tips and Burs are accessories to the air powered Bone drill (VARIOSURG with and without light) The intended use of the tips is based on the parent device. For the VarioSurg, in addition to the scaling functions, diamond coated tips are used for socket lift, sinus…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2713-2016·2016-09-07
Cardinal Health Recalls Arterial Blood Gas Kits Missing Safety Clasp
Cardinal Health is recalling specific lots of 9025TRU Arterial Blood Gas Kits because they are missing a locking clasp component, posing a potential safety risk.
Product
The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood sampling for pH, Blood Gas, Electrolyte and Metabolite Analysis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2709-2016·2016-09-07
Merge Cardio software recall due to incorrect patient data saving
Merge Healthcare is recalling Merge Cardio software versions 10.1 and 10.1.1 because reports may be saved to incorrect patient records.
Product
Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Image processing system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V645000·2016-09-07
Forest River Recalls 2017 Coachmen Viking Trailers Due to Roof Strut Defect
Forest River is recalling 2017 Coachmen Viking recreational trailers because a missing wire clip may allow the roof strut to detach, causing the roof to drop and increasing injury risk.
Product
COACHMEN — COACHMEN VIKING
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16T014000·2016-09-07
Tireco Recalls Milestar Tires with Incorrect Sidewall Markings
Tireco is recalling specific Milestar BS623 tires with incorrect sidewall markings that may lead to overloading and tire failure.
Product
TIRES:MARKINGS recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2691-2016·2016-09-07
Elekta Recalls HexaPOD evo RT Systems for Positioning Errors
Elekta is recalling 13 HexaPOD evo RT Systems because the treatment couch may not move fully to the correct 3D position, potentially leading to unrecognized positioning errors during radiotherapy.
Product
HexaPOD evo RT System Product Usage: The intended use of the device is the control of accurate patient positioning with assistance of a 3D Tracking System in a radiotherapy environment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2689-2016·2016-09-07
Mindray A7 Anesthesia Delivery System Recalled for Potential Oxygen Leak
Mindray is recalling 167 A7 Anesthesia Delivery Systems due to a potential leak on the back-up oxygen and air cylinder yokes.
Product
A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. Part numbers 0632F-PA0000X (US domestic) and 0632B-00014 (international)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16C007000·2016-09-07
Evenflo Recalls Evolve 3-in-1 Booster Seats Due to Harness Loosening Risk
Evenflo is recalling specific Evolve 3-in-1 Combination Booster Seats because children can access a button to loosen the harness, increasing injury risk in a crash.
Product
CHILD SEAT:HARNESS:STRAP/WEBBING recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2670-2016·2016-09-07
Philips Recalls UNIQ 1.0 Fluoroscopy Systems Due to Power Supply Failures
Philips is recalling 1,536 UNIQ 1.0 fluoroscopy systems because certain low-voltage DC power supplies have an increased failure rate.
Product
UNIQ 1.0: UNIQ FD10, 722026; UNIQ FD10/10, 722027; UNIQ FD20, 722028; UNIQ FD20/10 biplane, 722029; UNIQ FD10 OR Table, 722033; UNIQ FD10/10 OR Table, 722034; UNIQ FD20 OR Table, 722035; UNIQ FD20/20, 722038; UNIQ FD20/20 biplane OR Table, 722039; UNIQ FD20/15, 722058…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2672-2016·2016-09-07
Nakanishi Diamond Coated Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 30,719 diamond coated tips and burs because labeling failed to indicate they are single-use only, posing a cross-contamination risk.
Product
Diamond Coated Tips and Burs are accessories to the Ultrasonic Scaler (VARIOS 350 LUX, VARIOS 350, VARIOS 150 LUX, VARIOS 150). The intended use of the tips is based on the parent device. For the ultrasonic scalers and the sonic air scaler, the tips are used for various…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2674-2016·2016-09-07
Nakanishi Diamond Coated Dental Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 4,284 diamond coated dental tips because the packaging failed to indicate they are single-use only, posing a risk of cross-contamination.
Product
Diamond Coated Tips and Burs are accessories to the air powered dental handpiece (S-MAX pico) The intended use of the tips is based on the parent device. For burs used with the dental handpieces, the intended use is general dental actions such as removing carious material…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2669-2016·2016-09-07
Philips Recalls Allura Xper Systems Due to Power Supply Failure Risk
Philips is recalling 1,536 Allura Xper medical imaging systems because certain low-voltage DC power supplies have an increased failure rate.
Product
Allura Xper with release R8.2: Allura Xper FD10, 722026; Allura Xper FD10/10, 722027; Allura Xper FD20, 722028; Allura Xper FD20/10 biplane, 722029; Allura Xper FD10 OR Table, 722033; Allura Xper FD10/10 OR Table, 722034; Allura Xper FD20 OR Table, 722035; Allure Xper…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1474-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47477-5, Shade 02 (VF-N)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2706-2016·2016-09-07
Terumo Cardiovascular Procedure Kits Recalled for Incorrect Tubing Coating Labeling
Terumo is recalling 2,207 cardiovascular procedure kits because they are labeled as containing coated tubing but actually contain non-coated tubing.
Product
Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled containing Coated Tubing as follows: This product is intended for use only in the extracorporeal circuit for the cardiopulmonary bypass procedures for which the user designed it. This product is a…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1475-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47478-2, Shade 03 (MF-N)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1477-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48240-4, Shade 05 (D-G)
Category
Drug
Distribution
Distributed nationwide