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.
National Fish & Seafood, Inc. is recalling Matlaws R/B Shrimp Panko Tail-Off 21-25 due to potential undeclared milk content.
ICU is recalling 7,848 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting patient therapy.
National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Whiting Fillets because the product may contain undeclared milk.
ICU is recalling 214 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.
National Fish & Seafood, Inc. is recalling Lil Fisherman Pre Cooked Pollock Sticks because the product may contain undeclared milk.
St. Jude Medical is recalling 8,780 Proclaim 5 Elite implantable pulse generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.
National Fish & Seafood, Inc. is recalling Siemer Pre-Cooked Styled Cod Tails because the product may contain undeclared milk.
National Fish & Seafood, Inc. is recalling Schooner P/C Tilapia Fillets because the product may contain undeclared milk.
Merge Healthcare is recalling 555 Schiller PB 1000 Patient Data Modules because the analog output may not accurately reflect the pressure waveform used for fractional flow reserve calculations.
Natus Neurology is recalling 2,335 Elite 2 MHz OB probes because excessive background noise may mask the user's ability to hear heart rate or blood flow.
3CS Organics LLC is recalling Holle goat milk infant formula products that are not FDA approved and lack English labeling.
ICU Medical is recalling 900 units of 10-inch smallbore extension sets because the connection between the Female Luer and the NanoClave manifold may develop a leak.
National Fish & Seafood, Inc. is recalling Lil Fisherman Pre Cooked Pollock Nuggets because they may contain undeclared milk.
National Fish & Seafood, Inc. is recalling Matlaws Buffalo Popcorn Shrimp because the product may contain undeclared milk.
National Fish & Seafood, Inc. is recalling P/C Fish Sticks because they may contain undeclared milk, a major food allergen.
National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Styled Cod Fillets because the product may contain undeclared milk.
Carry-On Trailer is recalling 2017 Utility, Dump, and Enclosed trailers because a faulty breakaway box light may cause the circuit board to fail, increasing crash risk.
ICU Medical is recalling 100 units of 10-inch smallbore extension sets because the connection between the Female Luer and the NanoClave manifold may develop a leak.
ICU Medical is recalling 304 units of 18 cm Smallbore Extension Sets because the connection between the Female Luer and NanoClave manifold may leak.
National Fish & Seafood, Inc. is recalling pre-cooked fresh haddock fillets that may contain undeclared milk. The product was distributed to 24 states.
Nova Biomedical is recalling Stat Profile Prime Analyzers because a software defect could cause scheduled quality control tests to overwrite pending patient results.
St. Jude Medical is recalling 443 Infinity 5 Implantable Pulse Generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.
National Fish & Seafood, Inc. is recalling 365 Everyday Value Precooked Breaded Fish Squares because the product may contain undeclared milk.
ICU is recalling 363,892 Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting patient therapy.
Toshiba is recalling 90 APLIO 300 diagnostic ultrasound systems because they may display incorrect velocity trace values when using the Continuous Trace method.