State
73,738 recalls have nationwide distribution and so reach Washington. 8,535 additional recalls listed Washington specifically in their distribution scope.
Of the 8,535 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 2,404 (28%) are Severe.
Which agencies issued them
These figures cover only the 8,535 recalls whose distribution notice names Washington specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Cardinal Health is recalling AAMI 3 Nonreinforced Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Cardinal Health is recalling AAMI 3 non-reinforced surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Centurion Medical Products Corporation is recalling 1,720 dental kits because incomplete seals on the sterile packaging may compromise sterility.
Cardinal Health is recalling AAMI 3 non-radiation-protective surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Centurion Medical Products is recalling specific tracheostomy care kits and trays because incomplete seals may compromise sterility.
Centurion Medical Products Corporation is recalling specific sterile medical packs and trays because incomplete seals may compromise sterility.
Centurion Medical Products is recalling 1,986 circumcision trays because incomplete seals on the sterile packaging may compromise sterility.
Cardinal Health is recalling AAMI 3 nonreinforced surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Centurion Medical Products Corporation is recalling specific lots of sterile surgery kits because incomplete seals may compromise sterility.
Centurion Medical Products is recalling specific surgical trays because incomplete seals on the sterile packages may compromise sterility.
Centurion Medical Products is recalling 1,820 sterile nasal speculums due to incomplete package seals that may compromise sterility.
Cardinal Health is recalling AAMI 3 ROYALSILK SURGGOWN BNS XL units worldwide due to unknown levels of bioburden, microbiological flora, and particulate contamination.
B. Braun Medical is recalling 2,736 Y-Type Blood Sets due to a potential for leakage at the joint between the blood filters and tubing.
Centurion Medical Products Corporation is recalling sterile uterine sounds because incomplete seals may compromise sterility. The products were distributed nationwide and in Ghana.
Centurion Medical Products is recalling 60 Biopsy Trays because incomplete seals on the sterile package may compromise sterility.
Centurion Medical Products is recalling 108 units of Skin Prep Kits due to incomplete seals that may compromise sterility.
Cardinal Health is recalling specific lots of AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Cook Inc. is recalling Universa Soft Ureteral Stents because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Cook Inc. is recalling 13,388 Percutaneous Malecot Nephrostomy Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Cardinal Health is recalling AAMI 3 Non-Reinf Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Roche Diabetes Care is recalling Accu-Chek Aviva Plus test strips because they may fail to dose, potentially delaying treatment decisions.
Cook Inc. is recalling Bentson PTFE Wire Guides because they may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Clinical Diagnostic Solutions is recalling Medonic M-Series Hematology Analyzers due to a risk of sample misidentification and operator injury from exposed needles.
Cook Inc. is recalling Sof-Flex Double Pigtail Ureteral Stent Sets because the wire guide may be incorrectly loaded, potentially introducing a stiff tip into the patient.
Cook Inc. is recalling Kwart Retro-Inject Ureteral Stent Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.