State
73,809 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,054 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 708 (23%) are Severe.
Which agencies issued them
These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Toshiba is recalling 90 APLIO 300 diagnostic ultrasound systems because they may display incorrect velocity trace values when using the Continuous Trace method.
St. Jude Medical is recalling 9,529 Proclaim 7 Elite implantable pulse generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.
Toshiba is recalling 28 APLIO i-series diagnostic ultrasound systems because they may display incorrect velocity values when using the Continuous Trace method.
Arjo, Inc. is recalling 40,675 Flowtron ACS900 medical pumps worldwide because the device may fail to deflate the calf garment as intended without triggering an alarm.
Natus Neurology is recalling 2,335 Elite Obstetric probes because excessive background noise may mask fetal heart rate and blood flow monitoring.
NatureBox is recalling Mini Crispy Snickerdoodles because a cashew fragment was found during packing, posing a potential allergen risk.
3CS Organics LLC is recalling HIPP infant formula products because they are not FDA approved and lack full English labeling.
Toshiba American Medical Systems Inc. is recalling 307 APLIO 500 diagnostic ultrasound systems because they may display incorrect values when using the Continuous Trace method on Spectral Doppler.
Source Naturals Hydrogen Boost Capsules are being recalled because they contain low levels of undeclared boron. The recall covers 55,354 units distributed nationwide.
3CS Organics is recalling HIPP Organic infant milk products because they are not FDA approved and lack full English labeling.
3CS Organics LLC is recalling HIPP infant formula products because they are not FDA approved and lack complete English labeling.
Toshiba American Medical Systems is recalling seven XARIO 100 diagnostic ultrasound systems because they may display incorrect values when using the Continuous Trace method for velocity measurements.
3CS Organics LLC is recalling Topfer Lactana Bio infant and follow-up formula because the product is not FDA approved and lacks complete English labeling.
3CS Organics LLC is recalling HIPP Bio Combiotik infant formula products because they are not FDA approved and not all products are labeled in English.
3CS Organics LLC is recalling HOLLE organic infant formula products because they are not FDA approved and lack English labeling.
Beckman Coulter is recalling Synchron AQUA CAL Level 1 kits due to a sodium recovery shift that may affect system calibration.
Threshold Enterprises Ltd is recalling Source Naturals Renewal Antioxidant Tablets because they contain low levels of undeclared boron.
3CS ORGANICS LLC is recalling HIPP Anti-Reflux AR Bio-Spezialnahrung because the product is not FDA approved and lacks complete English labeling.
CryoLife, Inc. is recalling 52 On-X Prosthetic Heart Valves because the sewing ring type was mislabeled as Standard instead of Anatomic.
Natus Medical is recalling Olympic Pasteurmatic 3000 and 3500 systems because they do not fully meet current regulatory requirements due to design age and component obsolescence.
3CS Organics LLC is recalling specific Lebenswert infant and toddler milk formulas because the products are not FDA approved and lack full English labeling.
Lupin Pharmaceuticals is recalling Paroxetine Extended-Release Tablets because they failed dissolution testing during stability studies.
AMS Diagnostics is recalling 9 units of Medica ISE Module Calibrant A because the lot was not functioning properly and did not exhibit correct physical properties.
Mazda is recalling specific 2007-2012 CX-7, CX-9, and Mazda6 vehicles because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
TriMark is recalling specific door striker bolts used in ambulance door systems because they may fail during a crash, causing doors to open and increasing injury risk.