State
72,820 recalls have nationwide distribution and so reach Rhode Island. 3,042 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,042 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 569 (19%) are Severe.
Which agencies issued them
These figures cover only the 3,042 recalls whose distribution notice names Rhode Island specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
AVID Medical is recalling 45 Halyard DAVINCI TRUCUSTOM Foley catheter kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Medline Industries is recalling 2,262 medical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Medline Industries is recalling 94 surgical convenience kits nationwide because they contain a potentially contaminated component.
Midmark is recalling Digital ECG HD+12 and HD+15 units with specific IQecg plugin software versions due to a communication anomaly that may cause incorrect ECG waveforms and inaccurate heart rate calculations.
IMRIS Imaging Inc is recalling six ORT200 operating room tables because a mechanical failure could cause unintended movement and patient injury.
Medline Industries is recalling 106 C-section convenience kits distributed nationwide due to potentially contaminated components.
Midmark is recalling IQecg Digital ECG software due to a communication anomaly that may cause incorrect waveforms and inaccurate heart rate calculations.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 112 mcg tablets because they are subpotent. The recall covers nationwide distribution.
Medline Industries is recalling 419 surgical convenience kits because they contain a potentially contaminated component. The kits were distributed nationwide.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 150 mcg tablets because they may contain less active ingredient than labeled.
AVID Medical is recalling 120 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Apotex Corp. is recalling 6,972 bottles of Paxil CR 37.5mg tablets because the product failed dissolution specifications and 24-month stability testing.
ConMed is recalling specific suture anchors because they may contain incorrect patient implant cards, which could lead to incorrect device identification and traceability.
Henry Schein Inc. is recalling specific lots of Structur 2 SC Temporary Resin Cartridge Refills because they were distributed with incorrect packaging and Instructions for Use.
Henry Schein Inc. is recalling specific lots of Grandio Universal Nano-Hybrid Restorative Material capsules because they were distributed with incorrect packaging and Instructions for Use.
American Contract Systems Inc is recalling 30 units of Convenience Kits because the included Medline catheters did not meet performance specifications.
Hikma Pharmaceuticals is recalling specific lots of Ramipril 10 mg capsules because they failed impurity specifications for dicyclohexylurea.
Olympus is recalling 335 PowerSeal 5 mm Sealer & Divider devices because the outer shelf box is incorrectly labeled as a 37-cm device.
AVID Medical is recalling 78 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
American Contract Systems Inc is recalling 12 Convenience Kits containing Medline catheters because samples failed performance specifications.
AVID Medical is recalling 63 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Medline is recalling 45 Trach Tube Kits (SKU DYKM2330) due to a component labeling discrepancy. The recall covers units distributed in California.
AVID Medical is recalling 78 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
American Contract Systems Inc is recalling 30 units of Convenience Kits because Medline catheters failed performance specifications.
American Contract Systems Inc is recalling 30 units of Convenience Kits containing Medline catheters because samples failed performance specifications.