State
73,806 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.
Of the 8,536 recalls naming Washington we have scored against our rubric, 865 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,405 (28%) are Severe.
Which agencies issued them
These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Integra LifeSciences Corp. is recalling Tibial Total Ankle Prosthesis Trays because the labels and instructions for use list an incorrect metallic coating material symbol.
Wholesome Treats, Inc. is recalling Breads from Anna Classic Herb Bread Mix because the product contains undeclared flaxseed.
Integra LifeSciences is recalling 2,029 Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.
Ethicon, Inc. is recalling VICRYL, VICRYL Plus, and PDS sutures because the product inside may not match the sales unit carton and foil label.
Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels incorrectly identify the metallic coating material.
Integra LifeSciences is recalling Salto Talaris and Integra XT Revision ankle prostheses because the labels list an incorrect metallic coating material symbol.
Integra LifeSciences is recalling Salto Talaris and Integra XT Revision ankle prostheses because the labels incorrectly identify the metallic coating material.
Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels list an incorrect metallic coating material symbol.
Ethicon, Inc. is recalling VICRYL, VICRYL Plus, and PDS sutures because the product may not match the sales unit carton and foil label.
ConAgra Foods is recalling 145,380 cans of Hunts Tomato Paste No Salt Added due to potential mold caused by can damage.
Philips Medical Systems is recalling 7,209 foot switches used with specific imaging systems because bent pedals may prevent live fluoroscopy images or exposures.
Integra LifeSciences Corp. is recalling Talar Dome Total Ankle Prostheses because the labels list an incorrect metallic coating material symbol.
Siemens Healthcare Diagnostics is recalling 449 syngo Lab Data Manager systems due to software issues. The recall covers systems distributed in the US and nine other countries.
Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.
Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.
Roche Diagnostics is recalling 774 units of Albumin BCP reagent due to calibration failures and QC imprecision caused by elevated pH levels.
InvaGen Pharmaceuticals is recalling specific lots of Testosterone Cypionate Injection because of the presence of particulate matter. The affected vials were distributed nationwide.
Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.
Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.
Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels list an incorrect metallic coating material symbol.
Johnson Matthey Inc. is recalling Remifentanil HCl active pharmaceutical ingredient (API) because an unknown impurity exceeded specification limits.
Cordis Corporation is recalling Vista Brite Tip and Androit guiding catheters because frayed pieces of the mounting card were found inside the primary packaging.
Estee Lauder Inc is recalling 14,490 jars of Repairwear Laser Focus Line Smoothing Cream SPF 15 because the seal between the cap and jar is ineffective.
Toyota is recalling 2015-2017 Yaris vehicles because wire harnesses for side air bag sensors may crack and corrode, potentially causing air bags to fail to deploy or deploy improperly.
Toyota is recalling 2019 Sienna vehicles because incorrect welds in the passenger front door may affect air bag sensor readings, potentially causing unintended deployment or failure to deploy.