The Recall Desk

State

American Samoa product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33776–33800 of 73763

  • SevereNHTSA·19V395000·2019-05-24

    Starcraft All Star XL Diesel Fuel Heater Fire Risk Recall

    Forest River is recalling 2018-2019 Starcraft All Star XL diesel vehicles because the fuel heater may overheat, melt plastic, and cause a fire or engine stall.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V392000·2019-05-24

    Land Rover Recalls Range Rover Models for Door Latch Defect

    Jaguar Land Rover is recalling 2013-2016 Range Rover and 2014-2016 Range Rover Sport vehicles because doors may appear closed but are unlatched, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E036000·2019-05-23

    Meritor recalls steer axles due to insufficient lubrication risk

    Meritor is recalling specific steer axles because insufficient lubrication may damage wheel end bearings, potentially causing wheel separation and loss of vehicle control.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E035000·2019-05-23

    Transfer Flow Recalls Rear Brake Lines for Mobility Van Conversions

    Transfer Flow is recalling rear brake lines for mobility van conversions due to incorrect tube nut fittings that may cause a pressure drop in the braking system.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V386000·2019-05-23

    BMW Recalls 2019 X7 Vehicles Due to Head Air Bag Alignment Defect

    BMW is recalling 2019 X7 xDrive40i and xDrive50i vehicles because the driver and passenger head air bags may not be properly aligned, potentially impairing deployment and increasing injury risk.

    Product
    BMW — BMW X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V387000·2019-05-23

    GM Recalls 2016-2019 Chevrolet Express and GMC Savana for Window Glass Defect

    General Motors is recalling 2016-2019 Chevrolet Express and GMC Savana vehicles because rear-quarter windows may use tempered glass instead of laminated glass, increasing injury risk in crashes.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V390000·2019-05-23

    Land Rover Recalls 2016 Range Rovers for Door Latch Defect

    Jaguar Land Rover is recalling 28,671 2016 Range Rover and Range Rover Sport vehicles because a stuck spring may leave the left door unlatched, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19127·2019-05-23

    DICK'S Sporting Goods Recalls Ethos Pull-Up Assist Due To Laceration Hazard

    DICK'S Sporting Goods is recalling Ethos Pull-Up Assist equipment because a plastic clip can break, posing a laceration hazard. Seven reports of equipment breaking resulted in six lacerations.

    Product
    Ethos Pull-Up Assist
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19125·2019-05-23

    Far East Brokers Recalls Fabulous Home Pineapple Corer and Slicers

    Far East Brokers is recalling Fabulous Home Pineapple Corer & Slicers because the metal blade can detach, posing a laceration hazard.

    Product
    Fabulous Home Pineapple Corer & Slicers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1292-2019·2019-05-22

    Titanium 4000 capsules recalled for undeclared sildenafil and tadalafil

    D.B.P. Distribution is recalling Titanium 4000 capsules because they contain undeclared sildenafil and tadalafil and were marketed without an approved NDA or ANDA.

    Product
    Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1275-2019·2019-05-22

    Ethicon Intraluminal Staplers Recalled for Insufficient Firing Stroke

    Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH21A) because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Straight Intraluminal Staplers, 21 mm diameter, Model SDH21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1273-2019·2019-05-22

    Ethicon Endo-Surgery Recalls Endoscopic Curved Intraluminal Staplers

    Ethicon Endo-Surgery is recalling 434,614 endoscopic curved intraluminal staplers because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Endoscopic Curved Intraluminal Stapler, 29 mm diameter, Model ECS29A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1277-2019·2019-05-22

    Ethicon Endo-Surgery Recalls Straight Intraluminal Staplers Due to Firing Defect

    Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH29A) because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Straight Intraluminal Staplers, 29 mm diameter, Model SDH29A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1278-2019·2019-05-22

    Ethicon Endo-Surgery Recalls Straight Intraluminal Staplers Due to Firing Defect

    Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH33A) because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Straight Intraluminal Staplers, 33 mm diameter, Model SDH33A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·057-2019·2019-05-22

    Aurora Packing Recalls Raw Beef Products Due to E. coli O157:H7 Risk

    Aurora Packing Company is recalling approximately 62,112 pounds of raw beef products that may be contaminated with E. coli O157:H7. The products were shipped nationwide for further distribution and processing.

    Product
    Aurora Packing Company, Inc. — Aurora Packing Company, Inc. Recalls Beef Products Due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1385-2019·2019-05-22

    AmeriHerb Recalls Dried Dill Weed Potentially Contaminated with E. coli

    AmeriHerb International Inc is recalling 1 lb bags of dried dill weed potentially contaminated with E. coli. The product was distributed nationwide and to Canada.

    Product
    Dill weed c/s, Anethum graveolens, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1270-2019·2019-05-22

    Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke

    Ethicon Endo-Surgery is recalling 434,614 Curved Intraluminal Staplers (Model CDH33A) because they may have an insufficient firing stroke to break the washer and form staples.

    Product
    Curved Intraluminal Staplers, 33 mm diameter, Model CDH33A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1271-2019·2019-05-22

    Ethicon Endo-Surgery Recalls Endoscopic Curved Intraluminal Staplers

    Ethicon Endo-Surgery is recalling 434,614 Endoscopic Curved Intraluminal Staplers because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Endoscopic Curved Intraluminal Stapler, 21 mm diameter, Model ECS21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1268-2019·2019-05-22

    Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke

    Ethicon Endo-Surgery is recalling Curved Intraluminal Staplers, Model CDH25A, because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Curved Intraluminal Staplers, 25 mm diameter, Model CDH25A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1267-2019·2019-05-22

    Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke

    Ethicon Endo-Surgery Inc is recalling Curved Intraluminal Staplers, Model CDH21A, because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Curved Intraluminal Staplers, 21 mm diameter, Model CDH21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide