State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Michaels is recalling Ashland artificial poinsettia stems and bushes because mold may be present, posing a risk of respiratory or other infections.
Keystone is recalling 2016 Sprinter recreational vehicles because a wall-mounted television may break off, posing an injury risk to occupants.
Fagron, Inc. is recalling SyrSpend SF Grape Flavor suspending base due to the presence of yeast. The recall affects 148 bottles distributed nationwide.
Michaels is recalling Ashland holiday paper boxes because mold may be present, posing a risk of respiratory or other infections for consumers with compromised immune systems or mold allergies.
Iowa Mold Tooling is recalling certain Series III cranes because a valve bank cover may crack and fall off, creating a road hazard.
Accuray is recalling CyberKnife Robotic systems because the gun box mounting bracket may fail, allowing the gun box to fall and contact a patient.
Del Medical is recalling VS200 radiographic cassette holders and wall stands because they can suddenly fall to the ground and contact patients.
GE Medical Systems is recalling 2,111 Mavig Monitor Suspension Systems because a reported incident involved a suspension arm falling to the floor.
Del Medical, Inc. is recalling VS300 radiographic cassette holders and wall stands because the unit can suddenly fall to the bottom of its travel and contact a patient.
Zimmer Dental Inc is recalling specific dental implants because the instructions for use omitted safety information regarding the 3.7 mmD and 4.1 mmD Trabecular Metal models.
Bearded Brothers LLC is recalling BOLD The Greek energy bars due to mold. The recall covers 150 cases distributed nationwide.
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Zimmer Dental Inc. is recalling specific Trabecular Metal implants because safety information was omitted from the instructions for use.
Toshiba is recalling four INFX-8000V Bi-Plane X-Ray Interventional Systems because a software error caused dose data to be lost during specific imaging procedures.
Bulletproof Digital Inc is recalling FATwater Lemon bottles due to microbial growth detection. No pathogens were found.
Fagron, Inc. is recalling SyrSpend SF Suspending Base because the product contains yeast. The recall covers 88 bottles distributed nationwide.
Zimmer Dental Inc. is recalling specific dental implants because the latest instructions omitted information for certain models.
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Pharmacaribe LLC is recalling PulmoSal 7% Sodium Chloride inhalation solution because vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+).
Bulletproof Digital Inc is recalling 12,583 bottles of Berry FATwater due to microbial growth detection. No pathogens were detected.
Bearded Brothers LLC is recalling 128 cases of BOLD Coconut Curry energy bars due to mold. The product was distributed nationwide.
Merge Healthcare is recalling RadSuite picture archive systems because they may display incorrect Standardized Uptake Values (SUV). The recall covers 164 units distributed nationwide.
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Sandoz Inc. is recalling Candesartan Cilexetil Tablets, 16 mg, because the product failed impurities and degradation specifications at a 9-month stability timepoint.