State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Baxter Healthcare is recalling 54,528 bags of 5% Dextrose Injection because the bags may leak, compromising sterility.
Oscor, Inc. is recalling ATAR Disposable Extension Cables because they may separate from the connector during use, posing a risk to patients.
Bristol-Myers Squibb is recalling 48,180 bottles of Eliquis 5mg tablets because one bottle was found to contain 2.5mg tablets instead.
Daimler Trucks is recalling specific 2017-2018 Freightliner and Western Star trucks because a fuel pump drive gear may slip, causing sudden engine stalls and increasing crash risk.
Advanced Pharma Inc. is recalling QUELICIN (Succinylcholine Chloride) Injection due to a lack of assurance of sterility. The recall affects 2,350 units distributed nationwide.
Advanced Pharma Inc. is recalling 72 units of Potassium Phosphate IV bags nationwide due to a lack of assurance of sterility.
Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride bags because the company cannot assure the product's sterility.
O-Two Medical Technologies is recalling Adult Ventilation Timers because the flash rate may be twice the labeled rate, potentially affecting ventilation guidance.
National Fish & Seafood, Inc. is recalling Lil Fisherman Pre-Cooked Pollock Portions because the product may contain undeclared milk.
Natus Neurology is recalling 2,335 Elite 5 MHz Vascular Probes because excessive background noise may mask heart rate and blood flow signals.
National Fish & Seafood, Inc. is recalling Falcon Baie brand precooked fish portions because they may contain undeclared milk.
National Fish & Seafood, Inc. is recalling Schooner Pre Cooked Crunchy Fish Portions because the product may contain undeclared milk.
St. Jude Medical is recalling 373 Infinity 7 Implantable Pulse Generators because exposure to monopolar electrosurgical devices may cause a loss of neuromodulation therapy.
National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Fish Portions because the product may contain undeclared milk.
ICU is recalling Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting therapy.
National Fish & Seafood, Inc. is recalling 365 Everyday Value precooked breaded fish sticks because the product may contain undeclared milk.
National Fish & Seafood, Inc. is recalling pre-cooked cod portions that may contain undeclared milk. The product was distributed to 24 states.
St. Jude Medical is recalling 54 Infinity 5 Implantable Pulse Generators due to a risk of therapy loss if exposed to monopolar electrosurgical devices.
National Fish & Seafood, Inc. is recalling precooked breaded whiting portions because the product may contain undeclared milk.
National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Flounder Fillets because they may contain undeclared milk.
O-Two Medical Technologies is voluntarily recalling specific lots of Burn Relief hydrogel dressings because there is a lack of evidence validating the sterilization dose, posing a potential contamination risk.
National Fish & Seafood, Inc. is recalling Americas Choice Beer Battered Shrimp because the product may contain undeclared milk.
National Fish & Seafood, Inc. is recalling 205 cases of P/C FISH PTNS 5/4 LB because the product may contain undeclared milk.
St. Jude Medical is recalling 40 Infinity 7 Implantable Pulse Generators because exposure to monopolar electrosurgical devices during medical procedures may cause a loss of neuromodulation therapy.
ICU Medical is recalling 120 units of smallbore extension sets because the connection between the Female Luer and NanoClave manifold may develop a leak.