State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ethicon is recalling specific Proline suture products because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
Hitachi Medical Systems America Inc is recalling 264 Oasis MRI systems because an exposed stainless steel belt can cause finger cuts.
Avella of Deer Valley, Inc. is recalling 15 cassettes of fentanyl and bupivacaine due to potential bag leakage and lack of sterility assurance.
GE Medical Systems is recalling T2100 Microflex Drive Treadmills because unaddressed spare parts may cause uncontrolled walking belt motion during stress tests.
Ethicon is recalling 372 units of Proline Suture Blue 18" 7-0 because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
Ethicon is recalling specific Prolene suture products because a packaging design issue allows needles to perforate the package, posing risks of soft tissue injury or infection.
Ethicon is recalling specific Prolene suture units because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Wescam Inc is recalling 29 MX-10 surveillance laser systems because the ocular hazard distance is longer than specified, posing a risk of eye exposure.
Ethicon is recalling specific Proline suture products because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Siemens is recalling 197 units of Dimension Vista MULTI 1 SDIL diluent due to a potential defect in the vial cap septum that may cause inaccurate test results.
NewDeal SA is recalling TIBIAXYS devices because use may cause superficial or deep infections requiring antibiotic treatment or device removal.
T R Toppers, Inc. is recalling Chopped Chocolate Pretzel Pieces due to potential peanut contamination. Consumers should check for Lot 10481 and stop using the product.
Ethicon is recalling 300 units of Proline Suture 30" 6-0 Blue because a packaging design issue may allow the needle to perforate the package, posing injury or infection risks.
Opgen Inc is recalling AdvanDx QuickFISH Slides because they may show diminished performance before their expiration date.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.
Philips is recalling 32 Ingenuity Digital PET/CT Systems because a block connecting the patient pallet to the couch may be assembled incorrectly, potentially causing a misaligned screw.
Cardinal Health is recalling Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Stryker is recalling 180 reprocessed Harmonic Ace shears because they may display an error code preventing use.
Siemens Healthcare Diagnostics is recalling 1,446 units of Dimension Vista CTNI Sample Diluent because a defective cap septum may cause erroneously elevated test results.
Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.
Fx Solutions is recalling specific proton beam therapy heads due to a breach in the external blister packaging.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Fx Solutions is recalling specific lots of Humelock Offset Heads due to a breach in the external blister packaging.
Intel-GE Care Innovations LLC is recalling the Health Harmony Mobile application because patient data sometimes failed to sync with the backend database in a timely manner.