The Recall Desk

State

American Samoa product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38276–38300 of 73766

  • ModerateFDA (Drugs)·D-0826-2018·2018-05-30

    Exela Pharma Recalls Diclofenac and Misoprostol Tablets Due to Labeling Error

    Exela Pharma Sciences LLC is recalling 5,256 bottles of Diclofenac Sodium and Misoprostol tablets because some bottles were mislabeled with the wrong dosage.

    Product
    Diclofenac Sodium and Misoprostol Delayed Release Tablets 75 mg/0.2 mg, 60-count bottle, Rx Only, Manufactured by: Cipla Ltd., India; For: EAGLE PHARMACEUTICALS, INC., Woodcliff Lake, NJ 07677 USA, NDC 42367-111-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0837-2018·2018-05-30

    Lupin Recalls My Way Emergency Contraception Tablets for Lack of Approval

    Lupin Pharmaceuticals is recalling My Way emergency contraception tablets because the 2-pack configuration was marketed without the required regulatory approval.

    Product
    My Way (Levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5mg Levonorgestrel Tablets) per carton, GAVIS Pharmaceuticals, A Lupin Group Company; Mfg. for Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, UPC 3 43386-622-31 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0838-2018·2018-05-30

    Lupin Recalls My Way Levonorgestrel Tablets for Lack of Approved NDA

    Lupin Pharmaceuticals is recalling My Way (levonorgestrel) emergency contraception tablets because the 2-pack configuration was marketed without an approved New Drug Application.

    Product
    My Way (levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5mg Levonorgestrel Tablets) per carton, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202; Manufactured by: Lupin Limited, Pithampur (M.P.) - 454 775, INDIA, UPC 3 68180…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V351000·2018-05-29

    Western Star 4900 Trucks Recalled for Brake Hose Chafing Risk

    Daimler Trucks North America is recalling 2012-2019 Western Star 4900 trucks because front brake hoses may chafe against the hood, potentially reducing braking effectiveness.

    Product
    WESTERN STAR — WESTERN STAR 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V353000·2018-05-29

    Daimler Trucks Recalls 2017-2019 Models for Brake Caliper Bolt Issue

    Daimler Trucks North America is recalling 8,741 trucks because brake caliper mounting bolts may be insufficiently tightened, potentially reducing braking performance and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER, FCCC 5700, 4900, 4700, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V352000·2018-05-29

    Thomas Built Buses Recalling School Buses for Brake Bolt Issue

    Daimler Trucks North America is recalling 2,767 Thomas Built Buses Saf-T-Liner models from 2017-2019 because brake caliper mounting bolts may be insufficiently tightened.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER C2, SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V348000·2018-05-29

    Altec Recalls Aerial Devices Missing Towing Limit Placards

    Altec is recalling 2012-2018 aerial devices missing a placard stating maximum towing limits, which could lead to an overloaded receiver tube and increased crash risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V342000·2018-05-27

    GM Recalls 2018 Chevrolet Sonic for Driver Seat-Back Welding Defect

    General Motors is recalling 2018 Chevrolet Sonic vehicles because a joint in the driver's seat-back frame may not be properly welded, which could reduce strength in a crash.

    Product
    CHEVROLET — CHEVROLET SONIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V344000·2018-05-25

    Chrysler Recalls 2019 Jeep Cherokee for Engine Component Defects

    Chrysler is recalling 2019 Jeep Cherokee vehicles with 2.0L engines due to missing valve stem keepers or reversed camshaft caps that may cause engine failure and stalling.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V343000·2018-05-25

    2018 Jeep Wrangler Recall for Steering Shaft Weld Defect

    Chrysler is recalling 2018 Jeep Wrangler vehicles because a steering shaft weld may split, potentially causing loss of steering responsiveness and increasing crash risk.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V347000·2018-05-25

    Maserati Recalls 2018 Models Due to Front Sub Frame Weld Defects

    Maserati is recalling 2018 Levante, Ghibli, and Quattroporte vehicles because incomplete front sub frame welds may break, potentially causing loss of vehicle control.

    Product
    MASERATI — MASERATI LEVANTE, GHIBLI, QUATTROPORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V340000·2018-05-24

    GMC Recalls 2018 Terrain Models Due to Air Bag Module Software Defect

    General Motors is recalling 2018 GMC Terrain vehicles because the air bag control module may fail to power down, potentially preventing air bag deployment in a crash.

    Product
    GMC — GMC TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18166·2018-05-24

    IKEA Recalls SLADDA Bicycles Due to Belt Breakage and Fall Hazard

    IKEA is recalling approximately 4,900 SLADDA bicycles sold in the U.S. because the belt can break, posing a fall hazard. No injuries have been reported in the U.S.

    Product
    SLADDA bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18164·2018-05-24

    Bluefin Recalls Wireless Phone Chargers Due to Burn Hazard

    Bluefin International is recalling about 3,000 wireless phone chargers because they can overheat and cause burns. Consumers should stop using them and contact the company for a refund.

    Product
    Wireless phone chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0926-2018·2018-05-23

    AuroMedics Recalls Piperacillin and Tazobactam Injection Due to Glass Particulates

    AuroMedics Pharma LLC is recalling 77,400 vials of Piperacillin and Tazobactam for Injection due to confirmed visible glass particulate matter.

    Product
    PIPERACILLIN AND TAZOBACTAM — PIPERACILLIN AND TAZOBACTAM (PIPERACILLIN SODIUM AND TAZOBACTAM SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0839-2018·2018-05-23

    Apotex Recalls Subpotent Piperacillin and Tazobactam Injection Vials

    Apotex Inc. is recalling 121,693 vials of Piperacillin and Tazobactam for Injection due to high impurity levels that decreased the drug's potency.

    Product
    Piperacillin and Tazobactam for Injection, USP 3.375 gram/vial* 10-count Single Use Vials per carton, Rx Only, Mfg. by: Hospira Healthcare India Pvt. Ltd. Irungattukottai-602 105, India Mfg. for: Apotex Corp. Weston, FL 33326. NDC 60505-0687-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1842-2018·2018-05-23

    Medtronic Endo GIA Stapler Kits Recalled for Missing Sled Component

    Medtronic is recalling 171,271 Endo GIA stapler kits worldwide because a missing sled component may prevent staple formation, leading to bleeding or leakage.

    Product
    (1)BOX KITDE0183 APPENDIX LIPPE DETMOLD (KITDE0183) (2) KIT-DE-0083 APPENEKTOMIE KIT NAUENX1 (Item Number: KIT-DE-0083,KIT-DE-0083 APPENEKTOMIE KIT NAUENX1 Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of…
    Category
    Medical Device
    Distribution
    Distributed nationwide