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.
Advanced Pharma Inc. is recalling 180 bags of fentanyl injectable solution nationwide due to a lack of assurance of sterility.
Advanced Pharma Inc. is recalling 1,575 syringes of Phenylephrine HCl injectable solution because the company cannot guarantee the product is sterile.
Advanced Pharma Inc. is recalling 1,540 syringes of 2% Lidocaine HCl Injectable Solution because the company cannot assure the product's sterility.
Shimadzu is recalling 93 MobileDaRt Evolution mobile X-ray systems because the brakes may fail to engage when the operator releases the drive handle.
Heritage Pharmaceuticals is recalling 11,888 vials of Etomidate Injection because the drug was found to be subpotent. The recall is voluntary and nationwide.
Fujifilm is recalling 56 mobile X-ray systems because the braking mechanism may fail to engage when the handle is released.
Thor Motor Coach is recalling 110 motorhomes because the backup camera image may reverse, increasing crash risk. Dealers will install a harness to fix the issue.
ConvaTec is recalling specific lots of Feeding Tube Metric devices because an internal assessment found a potential breach in the sterile barrier.
AAP Implantate AG is recalling 25 units of the 20 mm Lambotte chisel due to a potential risk of breaking at the welded piece parts of the chisel body and knocking plate.
Advanced Pharma Inc. is recalling 2,580 syringes of Glycopyrrolate Injectable Solution nationwide due to a lack of assurance of sterility.
Osco Tank & Truck Sales is recalling 16,342 emergency vehicles built on 2012 Kenworth T440 and 2018 Peterbilt 348 chassis because brake lights may illuminate without the pedal being pressed.
Toyota is recalling specific 2019 models because the load capacity label text may become illegible, potentially leading to vehicle overload and increased crash risk.
Volkswagen is recalling 2019 Tiguan LWB vehicles because the tire information label contains inaccurate dimension and pressure specifications, which may increase crash risk.
Friendly Fruit Market is recalling Jansal Valley Cocoa Dusted Chocolate Covered Almonds because the product contains undeclared sesame seeds.
ConvaTec is recalling Nelaton Urinary Catheters because an internal assessment found a potential breach in the sterile barrier, which could compromise the device's sterility.
Cambridge Elevating is recalling approximately 680 home elevators because the landing door can unlock without the elevator present, posing a fall hazard.
CP Medical Inc is recalling Plain and Chromic Gut Absorbable Surgical Sutures because routine endotoxin testing showed an out-of-limit result, potentially compromising sterility.
The FDA is recalling 850 units of the Covidien Force TriVerse electrosurgical device due to potential sterile packaging compromise.
Siemens is recalling 5,373 Dimension Vista 1500 analyzers because specific water purification modules may cause falsely elevated triglyceride results.
ACell, Inc. is recalling one lot of Gentrix Surgical Matrix Thick because a sample failed to meet tensile strength specifications.
Siemens is recalling 5,373 Dimension Vista 500 analyzers because specific Millipore water purification modules may cause falsely elevated triglyceride results.
Akorn Inc is recalling Hydrocortisone and Acetic Acid Otic Solution because routine stability testing revealed the drug was sub-potent.
ConvaTec is recalling 124,000 FilterFlow Suction Handles because an internal assessment found a potential breach in the sterile barrier.
ConvaTec, Inc. is recalling Forceps Blue, disposable sterile forceps, because an internal assessment confirmed the potential for a breach in the sterile barrier.
ACell, Inc. is recalling one lot of Gentrix Surgical Matrix Thick devices because a sample failed to meet tensile strength specifications.