State
73,827 recalls have nationwide distribution and so reach Massachusetts. 8,252 additional recalls listed Massachusetts specifically in their distribution scope.
Of the 8,252 recalls naming Massachusetts we have scored against our rubric, 1,179 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,360 (29%) are Severe.
Which agencies issued them
These figures cover only the 8,252 recalls whose distribution notice names Massachusetts specifically. The 73,827 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 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.
Baxter Healthcare is recalling 295,200 bags of 0.9% Sodium Chloride Injection due to a lack of assurance of sterility and potential for leaking.
ICU is recalling 71 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.
ICU is recalling 21,703 Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting therapy.
ICU is recalling 10,609 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting patient therapy.
National Fish & Seafood, Inc. is recalling Matlaws flounder fillets because they may contain undeclared milk. The product was distributed in 24 states.
National Fish & Seafood, Inc. is recalling pre-cooked minced pollock portions because they may contain undeclared milk.
National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Styled Haddock Fillets because they may contain undeclared milk.
Arrow International is recalling Glide Thru Peel-Away Sheath/Dilator Introducers because hub tabs may detach prematurely during use.
GE Healthcare is recalling Carestation 620, 650, and 650c monitors due to potential for elevated FiCO2 readings and unexpected system malfunctions.
ICU is recalling 180 Plum A+ Infusion Systems because battery issues may cause an E321 error code and interrupt therapy.
Toshiba American Medical Systems is recalling XARIO 200 diagnostic ultrasound systems because the Continuous Trace method may display incorrect velocity trace values.