State
72,940 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 5 (20%) are Severe.
Which agencies issued them
These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 1,320 HEZI brand power strips are being recalled because they have an ungrounded metal enclosure that poses an electrocution hazard if energized.
Gulf Stream is recalling 2026 Trail Boss and Ameri-Lite trailers because reversed taillight wires may cause turn signals to activate in the wrong direction.
About 4,100 Energizer Large Power Indicator Lanterns are being recalled because the lithium-ion batteries installed in them can overheat, posing a burn hazard.
AVID Medical is recalling 132 Halyard Organ Recovery OR Packs, kit code LLOG1000-15, because the devices are not suitable for organ transplant.
AVID Medical is recalling 52 Halyard Organ Recovery OR Packs because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
MediNatura is recalling all lots within expiry of ClearLife Allergy Nasal Spray, Extra Strength, after the products were found to contain yeast, mold and Achromobacter.
AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
MediNatura is recalling all lots within expiry of ReBoost Nasal Spray after the products were found to contain yeast, mold and microbial contamination identified as Achromobacter.
Securitas Healthcare is recalling 5,627 Arial 900 MHz Call Stations, model CSK200-900, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.
Medline is recalling 1,611,081 Hudson RCI medium concentration oxygen masks after multiple complaints of tubing disconnecting, which may lead to shortness of breath and hypoxia.
Imprimis NJOF is recalling 778 boxes containing 15,540 pre-filled syringes of Dexamethasone and Moxifloxacin intraocular injection over glass-like particles.
CareFusion 303 is recalling 2,079 BD Pyxis ES Enterprise Server systems over a software issue that may result in equipment not receiving timely updates of patient or medication information.
Imprimis NJOF is recalling 596 boxes containing 11,920 pre-filled syringes of Dexamethasone, Moxifloxacin and Ketorolac intraocular injection over glass-like particles.
IMRIS Imaging is recalling 122 HFD100 Head Fixation Devices because a torque screw may crack or separate, which could lead to inadequate head stabilization and risk of patient injury.
MAYEJ Comercializadora is recalling 1,288 boxes of Italian Parsley over the pathogen Cyclospora cayetanensis.
Securitas Healthcare is recalling 1,898 Arial 900 MHz Call Stations, model CSK200-900MR, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.
Imprimis NJOF is recalling 314 boxes containing 6,280 pre-filled syringes of Tri-Moxi triamcinolone and moxifloxacin intraocular injection over glass-like particles.
Roche Diagnostics is recalling 1,300 Elecsys Anti-TSHR cassettes because results vary by instrument platform and calibrator lots vary, which may lead to incorrect diagnosis or treatment.
Philips North America is recalling 13,470 Smart-hopping 2.0 AP 1.4 GHz patient monitors because the MX40 could not reconnect to the PIC iX when signal strength changed quickly.
Meridian Bioscience is recalling 211 units of the Revogene C. difficile assay because affected lots show a decline in performance over time, which may lead to false-negative results.
Remote Diagnostic Technologies is recalling 7,129 Philips Tempus Pro Patient Monitors because intracranial and bladder pressure measurements have not been tested or validated for accuracy.
Sophysa is recalling 105 Pressio 2 ICP Monitoring Systems following customer complaints of the Pressio monitor rebooting.
Integra LifeSciences is recalling 5,116 Codman CereLink ICP Sensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.
SpecGx is recalling 74,544 bottles of Oxycodone and Acetaminophen CII Tablets, 7.5 mg/325 mg, because of the potential for the imprint to be missing on tablets.
SpecGx is recalling 287,988 bottles of Oxycodone and Acetaminophen CII Tablets, 10 mg/325 mg, because of the potential for the imprint to be missing on tablets.