State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Novel Laboratories is recalling Zolpidem Tartrate sublingual tablets because the packaging fails to meet child-resistant closure requirements, posing a risk of poisoning to children.
WalkMed Infusion, LLC is voluntarily recalling specific lots of 90-inch IV administration sets due to the potential presence of particulate matter in or on the devices.
WalkMed Infusion is voluntarily recalling T100-000F IV sets due to the potential presence of particulate matter in or on the devices.
WalkMed Infusion is voluntarily recalling specific lots of 90-inch IV administration sets due to the potential presence of particulate matter in or on the devices.
WalkMed Infusion is voluntarily recalling specific lots of 90-inch IV administration sets due to the potential presence of particulate matter in or on the devices.
WalkMed Infusion is voluntarily recalling specific lots of IV sets with 0.22 micron filters due to the potential presence of particulate matter in or on the devices.
WalkMed Infusion is voluntarily recalling Triton Administration Sets due to the potential presence of particulate matter in or on the devices.
Biomet, Inc. is recalling 5,458 units of the TSP Hip Fracture Plating System because screws may fracture during implantation, potentially leaving a foreign body in the patient.
WalkMed Infusion is voluntarily recalling specific lots of Triton IV administration sets due to the potential presence of particulate matter in or on the devices.
Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause them to appear lumpy and have an unpleasant taste and odor.
Bolthouse Farms is recalling eight varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
Bolthouse Farms is recalling 8 varieties of protein drinks because spoilage may cause them to appear lumpy and have an unpleasant taste and odor.
Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
Siemens Medical Solutions is recalling 50 units of Syngo.via PACS software due to incorrect volume calculation values. A software update is available to resolve the error.
Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur XPT system software versions V1.0.1 through V1.1 due to eight identified issues that may affect test results.
WalkMed Infusion is voluntarily recalling specific IV administration sets due to the potential presence of particulate matter in or on the devices.
WalkMed Infusion is recalling Triton and Triton FP infusion pumps due to unapproved changes to software, specifications, and intended use.
Bolthouse Farms is recalling eight varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.
DePuy Synthes is voluntarily recalling TFNA Blade/Screw Guide Sleeves because a manufacturing defect may prevent proper use, potentially causing surgical delays.
Sun Pharmaceutical Industries is recalling 16,085 bottles of Bupropion Hydrochloride Extended Release Tablets because they failed dissolution specifications.
Forest River is recalling 39 Glaval Titan II Low Floor buses due to frames that may crack, potentially reducing driver control and increasing crash risk.
Braun is recalling 2016 MXV vehicles because the passenger seat electrical harness may be crushed, potentially preventing airbag deployment in a crash.
Chrysler is recalling 2015 RAM 2500 and 3500 trucks because inadequate welds on front track bar brackets may separate, reducing steering response and increasing crash risk.