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.
BioMerieux SA is recalling ETEST OXACILLIN OX 256 WW F100 in vitro diagnostic strips due to quality control failures that may cause false resistant results.
Zimmer Dental Inc. is recalling 356 GemLock RHD2.5 Hex Drivers because a manufacturing defect may prevent the tool from properly engaging dental fixtures.
HealthPostures is recalling IntimateRider chairs and RiderMate benches because loose stitching on the cloth covers can cause falls and injuries.
Medacta is recalling 12,768 GMK knee system inserts nationwide due to a reported 0.1% occurrence rate of post-operative screw back-out.
Rocky Mountain Bicycles is recalling 2018 Altitude, Instinct, and Pipeline models because improperly secured brake cable housing can cause brake failure and crashes.
Zimmer Dental Inc. is recalling 30 surgical kits because a manufacturing defect may prevent the driver from properly engaging dental implants.
Zimmer Dental Inc. is recalling 891 Tapered Screw-Vent Implant System surgical kits because a manufacturing defect in the driver's hex feature may prevent proper engagement with dental implants.
Advanced Pharma Inc. is recalling NitroGlycerin 1 mg/10 mL syringes because stability data does not support the expiry dates. The recall affects 4,800 syringes distributed nationwide to hospitals.
B. Braun Medical Inc. is recalling 2,576 containers of 0.25% Acetic Acid Irrigation USP due to the presence of polyethylene particulate matter.
Philips is recalling 157 medical imaging systems because a software option prevents correct export of measurement data to external destinations.
Claris Lifesciences Inc. is recalling Ciprofloxacin in Dextrose Injection because the product is superpotent. The recall is voluntary and nationwide.
Invivo Corporation is recalling 4,535 Xper Flex Cardio Physiomonitoring systems because of intermittent communication between the host system and the device.
Osmotica Pharmaceutical Corp is voluntarily recalling 9,919 bottles of subpotent Methylphenidate Hydrochloride Extended-Release Tablets distributed nationwide.
Teva Pharmaceuticals is recalling Amethyst oral contraceptive tablets because the packaging incorrectly states that Week 4 tablets are inactive, when all tablets are active.
Advanced Pharma Inc. is recalling 680 syringes of NitroGlycerin injection because stability data does not support the product's expiry dates.
Advanced Pharma Inc. is recalling NitroGlycerin injection syringes because stability data does not support the product's expiry date.
Implant Direct is recalling 560 Spectra System/Legacy Guided Surgery Handle Kits because some guide inserts do not meet specifications, preventing proper drill passage.
Advanced Pharma Inc. is recalling NitroGlycerin 100 mcg/mL syringes because stability data does not support the product's expiry date.
Zimmer Dental Inc. is recalling 166 surgical kits because a manufacturing defect may prevent the driver from properly engaging dental implants.
Renaissance Lakewood, LLC is voluntarily recalling 24,569 bags of Fluconazole Injection, USP, 2 mg/mL, due to superpotency. The FDA classified this as Class III.
Osmotica Pharmaceutical Corp is voluntarily recalling 10,064 bottles of subpotent Methylphenidate Hydrochloride Extended-Release Tablets nationwide.
Newmar is recalling 2017 Bay Star, Bay Star Sport, and Canyon Star motorhomes because missing plugs in the brake system may cause fluid leaks or air ingestion, increasing stopping distance.
MV Agusta is recalling 2015-2017 F4 RC and F4 RR motorcycles because the front brake master cylinder may fail, increasing crash risk.
Tiffin is recalling 2009-2018 motorhomes because Kidde fire extinguishers may clog or detach, potentially failing to work during a fire.
Vilo Home is recalling Marseille dining benches because the foam seat cushion and base can crack, causing the bench to collapse and posing a fall hazard.