State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Whole Foods Market is recalling Black Bean Burritos because they contain undeclared peanut protein. Consumers should not eat the product.
Whole Foods Market is recalling Quesadilla Veggie products because they contain undeclared peanut protein. The recall covers units sold in 13 states and Washington, D.C.
Electrolux is recalling about 250 Kenmore Elite dual fuel ranges sold at Sears because the burner flame can go out while gas is on, posing fire and burn risks.
Whole Foods Market is recalling Pico De Gallo Salsa products due to undeclared peanut protein. Consumers with peanut allergies should not consume the affected items.
Whole Foods Market is recalling 193 pounds of Chili Firehouse HSH due to undeclared peanut protein. The product was sold in 13 states and Washington, D.C.
Whole Foods Market is recalling Tofu Grilled Lime Chipotle because it contains undeclared peanut protein. Consumers with peanut allergies should not eat the product.
Whole Foods Market is recalling shrimp burritos because they contain undeclared peanut protein, posing a risk to individuals with peanut allergies.
Whole Foods Market is recalling Adobo Enchiladas and Dirty Rice products due to undeclared peanut protein in cumin.
Gourmet Kitchen, Inc. is recalling Lobster & Shrimp Spring Rolls because they may contain peanut protein. The recall covers 120 boxes distributed nationwide.
Natural Foodworks Group is recalling Purely Elizabeth Cranberry Cashew Ancient Grain Muesli because it contains undeclared sulfur dioxide.
Alvogen, Inc. is recalling Nitrofurantoin Monohydrate/Macrocrystalline capsules because they failed a dissolution specification test.
Akorn, Inc. is recalling specific lots of Sulfamethoxazole and Trimethoprim Oral Suspension because the sulfamethoxazole failed to meet dissolution specifications.
Synthes, Inc. is recalling 8,175 TFNA Proximal Femoral Nails because the locking mechanism was assembled too close to the top, potentially causing surgical delays.
Akorn, Inc. is recalling specific lots of Sulfamethoxazole and Trimethoprim Oral Suspension because the sulfamethoxazole component failed to meet dissolution specifications.
BioHorizons is recalling 48 units of the Tapered HD Upgrade Set because they were packaged with a stainless steel drill instead of the correct titanium component.
Apotex Inc. is voluntarily recalling 6,467 units of Olanzapine 10 mg orally disintegrating tablets because the drug is subpotent.
Philips Medical Systems is recalling 975 nuclear gamma cameras because the collimator exchange carriage and storage cabinet were misaligned.
Akorn, Inc. is recalling 8,400 cups of Sulfamethoxazole and Trimethoprim oral suspension because the sulfamethoxazole failed to meet dissolution specifications.
Mission Pharmacal is recalling 1,992 kits of Sodium Sulfacetamide 9% and Sulfur 4.5% Wash due to microbial contamination.
Fujifilm Medical Systems is recalling Synapse Cardiovascular software versions v4.0.8 and v4.0.8 SR1 because patient demographics in exported reports may not match the clinical reports.
Stryker Howmedica Osteonics is recalling four 80 mm Kinemax Stem Extenders because they were shipped in boxes labeled for the 80 mm part but contained 40 mm extenders.
Cipla Limited is recalling 140,625 vials of Levalbuterol Inhalation Solution because the product failed impurity specifications. The affected lot is distributed nationwide.
Zimmer Surgical Inc is recalling 36 units of the 100 mL Hemovac Mini Evacuator because the shipper carton contained only one Instructions for Use (IFU) instead of one per sales unit.
Spinal Elements, Inc. is recalling 588 Mercury lordosed rods because some lack required product identification markings, interrupting device traceability.
Medtech Products, Inc. is recalling Monistat 1 Simple Cure because the distributed units lack the required topical cream.