State
73,584 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.
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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Newmar is recalling specific 2018-2019 motorhomes because the instrument panel brightness cannot be adjusted, creating glare that may increase crash risk.
Amazon is recalling Calmer Solutions Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Chrysler is recalling Mopar All-Weather Floor Mat Kits for 2019-2020 Ram 1500 vehicles because the mats may interfere with the accelerator pedal, increasing crash risk.
Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because incorrect tire pressure settings may prevent warning lights from illuminating, increasing crash risk.
ZF North America is recalling specific curtain air bag inflators where improperly crimped diffusers may separate during deployment, potentially preventing proper air bag inflation.
Chrysler is recalling 2019-2020 Ram 1500 trucks with adjustable pedals because floormats may prevent the accelerator from returning to the idle position, increasing crash risk.
BMW is recalling 2021 X7 models for tire information labels with incorrect specifications. The labels may not match the actually installed tires, potentially causing drivers to select wrong tires.
Ferring Pharmaceuticals is recalling 184,325 vials of Desmopressin Acetate Nasal Spray because the drug is superpotent. The recall is voluntary and nationwide.
Ferring Pharmaceuticals is recalling 29,371 vials of STIMATE nasal spray because the drug is superpotent. The recall is voluntary and nationwide.
Ferring Pharmaceuticals is recalling 15,175 bottles of DDAVP Nasal Spray because the drug may be superpotent. The recall is voluntary and nationwide.
Arjo Huntleigh is recalling 145 Citadel Plus Bariatric Bed Frame Systems because Modular Junction Box cables can melt, potentially affecting bed functionality.
Volkswagen is recalling 2020 and 2021 Atlas vehicles due to driver's side headlights that may have been aimed too low during production. This misalignment fails to meet federal safety standards and reduces driver visibility.
PACCAR is recalling approximately 1,097 certain 2020-2021 Kenworth and Peterbilt heavy trucks with Watson and Chalin steerable lift axle suspension systems. The pivot bolts may be too short to properly engage the locking nuts, risking separation from the suspension and potential vehicle crashes.
CMP Group is recalling aluminum dock ladders because sharp edges on the steps can cut consumers. About 750 units were sold online from 2017 to 2020.
Nobel Biocare is recalling 188 NobelReplace dental implants because the cap label incorrectly lists measurements as 5.0x8mm instead of the actual 4.3x10mm.
Precision Valve & Automation is recalling three PVA PREVENT emergency ventilators due to a software error that may cause false alarms or incomplete air delivery cycles.
Certain 2020 Audi SQ5 and Q5 vehicles and 2020-2021 Volkswagen models have improperly welded front seat frames. In a rear-end crash, the defective welds could fail and reduce occupant restraint, increasing the risk of injury.
Synthes (USA) Products LLC is recalling 191 units of DePuy Synthes Trauma LCP One-Third Tubular Plates because dimensional features may be out of tolerance, potentially reducing locking strength.
Chembio Diagnostics is recalling 7,674 kits of the DPP COVID-19 IgM/IgG System because the FDA revoked its Emergency Use Authorization due to performance issues.
Communicorp is recalling 6-inch plush Aflac Doctor Duck promotional items because the buttons on the lab coat contain lead levels exceeding federal standards.
Lannett Company, Inc. is recalling specific batches of Prednisone Tablets due to a labeling error where 2.5 mg bottles contained 10 mg tablets.
Argon Medical Devices is recalling 1,000 units of ClosureFast Micro Introducer Sheath Sets because the sterile products were manufactured under one lot with different expiration dates.
Calvin Scott & Company is recalling specific lots of Phentermine HCL capsules because light-sensitive products were repackaged in transparent pouches.
Calvin Scott & Company is recalling Topiramate 25mg tablets because light-sensitive drugs were repackaged in transparent pouches, violating CGMP standards.
CareFusion 303, Inc. is recalling Alaris EtCO2 Module Model 8300 units because LED display segments may appear dim, potentially affecting the visibility of infusion or patient monitoring values.