The Recall Desk

State

American Samoa product recalls

73,478 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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23001–23025 of 73503

  • ModerateFDA (Drugs)·D-0026-2022·2021-10-27

    Omeprazole Magnesium Acid Reducer Capsules Recalled for Staple Contamination

    Dr. Reddy's Laboratories is recalling Acid Reducer (Omeprazole Magnesium) 20 mg capsules nationwide because staples have been found co-mingled with capsules in bottles.

    Product
    ACID REDUCER — ACID REDUCER (OMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0024-2022·2021-10-27

    AirDuo Digihaler inhalation powder subpotent drug recall

    Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some batches do not deliver the labeled amount of salmeterol, a critical active ingredient for asthma and COPD control.

    Product
    AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd. by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-129-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0151-2022·2021-10-27

    HemosIL Liquid Anti-Xa Assay On-Board Stability Issue Recall

    Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa, a coagulation assay measuring heparin activity, due to reduced on-board instrument stability from 7 days to 5 days.

    Product
    HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACLTOP¿ Family, ACL TOP Family 50 Seriest and ACL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0149-2022·2021-10-27

    Heparin Activity Assay Labeling Correction: Reduced On-Board Stability

    Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa kits due to a labeling correction. The on-board stability window has been reduced from 7 to 5 days.

    Product
    HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACL TOP¿ Family, ACL TOP Family 50 Seriest and ACL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0126-2022·2021-10-27

    Plastic Tenaculum Surgical Instruments Recalled for Unconfirmed Manufacturing Standards

    Stradis Medical is recalling plastic tenaculum surgical instruments because the manufacturer cannot confirm they were produced in accordance with required design and manufacturing standards. Approximately 2,483 kits were distributed nationwide and to Canada.

    Product
    Tenaculum, Plastic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0021-2022·2021-10-27

    AirDuo Digihaler 113/14 Inhalation Powder Subpotent Drug Recall

    Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some units contain less salmeterol than the labeled dose. The affected sample batch was distributed nationwide.

    Product
    AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC , Frazer, PA 19355, Manufactured in Ireland, NDC 59310-520-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0027-2022·2021-10-27

    Lupin Imipramine Pamoate Capsules Recalled for Failed Dissolution Test

    Lupin Pharmaceuticals is recalling approximately 1,902 bottles of Imipramine Pamoate Capsules 125 mg due to out-of-specification results in dissolution testing at the 9-month stability checkpoint.

    Product
    IMIPRAMINE PAMOATE — IMIPRAMINE PAMOATE (IMIPRAMINE PAMOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0016-2022·2021-10-27

    Coppertone Pure & Simple Kids 50 Sunscreen Spray Recalled for cGMP Deviations

    Beiersdorf Inc. is voluntarily recalling Coppertone Pure & Simple kids 50 Sunscreen Spray due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 70,320 cans distributed nationwide.

    Product
    Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02882 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateCPSC·22008·2021-10-27

    5.11 Tactec Plate Carriers Recalled Due to Injury Hazard

    5.11 Inc. is recalling about 45,170 Tactec Plate Carriers (style 56100) because the cable in the quick release system can separate from the handle, preventing swift removal in an emergency. No injuries have been reported.

    Product
    56100 Tactec™ Plate Carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0020-2022·2021-10-27

    GlipiZIDE Extended-Release Tablets 2.5 mg Nationwide Recall

    American Health Packaging is recalling GlipiZIDE Extended-Release Tablets 2.5 mg (Lot #194141) nationwide because dissolution test results exceeded specification, which may affect the drug's effectiveness.

    Product
    GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx only, Manufactured by: Patheon Pharmaceuticals Inc., Cincinnati, OH 45237; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054. Carton NDC#…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E090000·2021-10-26

    WABCO Trailer ABS Systems Recalled for Brake Pressure Loss Risk

    WABCO is recalling certain Trailer ABS Systems because improperly tightened screws may loosen, causing pressure loss and potential brake failure.

    Product
    SERVICE BRAKES, AIR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V837000·2021-10-25

    2020-2023 IC Bus School Buses Recalled for Engine Shut Down Risk

    Navistar is recalling 2020-2023 IC Bus CESB school buses due to an engine control module defect that may cause unexpected engine shutdown while driving, increasing the risk of crashes and emergency evacuation situations.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V835000·2021-10-25

    Tesla Model 3 and Model Y suspension fasteners recalled for loosening

    Tesla is recalling 2019-2021 Model 3 and 2020-2021 Model Y vehicles where front suspension lateral link fasteners may loosen, potentially causing wheel misalignment and increasing crash risk.

    Product
    TESLA — TESLA MODEL 3, MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V834000·2021-10-25

    2020-2023 Tesla Model 3 Curtain Airbag Deployment Safety Defect

    Tesla is recalling certain 2020-2023 Model 3 vehicles because the side curtain airbag may be improperly secured to the roof rail and could twist, deploying incorrectly during a crash and increasing risk of injury or ejection.

    Product
    TESLA — TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·21V836000·2021-10-25

    Yamaha Recalls 2021 Tracer 9 GT for Incorrect VIN Label

    Yamaha is recalling 2021 Tracer 9 GT motorcycles because the VIN on the certification label may not match the vehicle's stamped VIN, potentially preventing owners from receiving safety recall remedies.

    Product
    YAMAHA — YAMAHA TRACER 9 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V833000·2021-10-23

    Ferrari Recalls 458 and 488 Models for Brake Fluid Leak Risk

    Ferrari is recalling specific 458 and 488 models because the brake system may leak fluid, potentially causing a loss of braking ability.

    Product
    FERRARI — FERRARI 488 GTB, 458 ITALIA, 488 SPIDER, 458 SPECIALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22007·2021-10-22

    Walmart Better Homes and Gardens Room Spray Recalled for Dangerous Bacteria

    Walmart is recalling Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones due to contamination with Burkholderia pseudomallei bacteria. CDC testing identified the hazard and is investigating a cluster of four melioidosis cases, including two deaths.

    Product
    Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V830000·2021-10-22

    2021-2022 Forest River XLR Toy Hauler Recalled for Missing Furnace Protective Panel

    Forest River is recalling certain 2021-2022 XLR Toy Hauler recreational vehicles with a missing protective panel between the furnace and cargo area. The missing panel could allow cargo to contact furnace wiring, creating a fire hazard.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V828000·2021-10-22

    2022 Coachmen Catalina Travel Trailer Recall for Unsealed Furnace Panel

    Forest River is recalling 2022 Coachmen Catalina travel trailers because an unsealed panel between the furnace and cooktop could cause an inverted flame, increasing fire risk.

    Product
    COACHMEN — COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V829000·2021-10-22

    2022 Forest River XLR Toy Hauler Recalled for Electrical Fire Risk

    2022 Forest River XLR Toy Hauler RVs are recalled due to incorrect wiring lacking required over-current protection. The defect can cause electrical shorts and fire; dealers will replace the wiring and breaker at no cost.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V832000·2021-10-22

    Mercedes-Benz Recalls 2021 Models for Rear Window Bonding Defect

    Mercedes-Benz is recalling certain 2021 GLE and GLS models because the rear window may be insufficiently bonded, posing a road hazard risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 580, AMG GLE53, GLS580, GLS450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·21V831000·2021-10-22

    2022 BMW X4 Rear License Plate Lamp Illumination Defect

    BMW is recalling certain 2022 X4 vehicles because the rear license plate may not be properly illuminated, violating federal safety standards and potentially creating visibility issues for other drivers.

    Product
    BMW — BMW X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V827000·2021-10-21

    Orange EV Recalls T-Series Trucks Due to Steering Bolt Issue

    Orange EV is recalling 2019-2021 T-Series electric trucks because a steering bolt may loosen, potentially causing loss of steering.

    Product
    ORANGE EV — ORANGE EV T-SERIES ELECTRIC TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide