State
73,741 recalls have nationwide distribution and so reach Massachusetts. 8,248 additional recalls listed Massachusetts specifically in their distribution scope.
Of the 8,248 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 2,356 (29%) are Severe.
Which agencies issued them
These figures cover only the 8,248 recalls whose distribution notice names Massachusetts specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Terumo Medical Corporation is recalling 81,000 30G needles due to a potential loss of package integrity that may compromise sterility.
Terumo Medical Corporation is recalling 729,000 Sur-vet Needles because a potential loss of package integrity may compromise the sterility of the product.
Deva Holding AS is recalling Temozolomide capsules because manufacturing deviations allowed possible cross-contamination with beta-lactam products.
Pharma-Natural Inc. is recalling Tusslin cough syrup because it was manufactured with current good manufacturing practice violations, including a lack of process validation.
Siemens is recalling one AXIOM Artis dBC X-ray system because a power supply defect may prevent X-ray generation during procedures.
Siemens Medical Solutions is recalling three Artis zee biplane MN units due to a power supply tolerance issue that may prevent X-ray generation during procedures.
Siemens is recalling four AXIOM Artis FA units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.
Pharma-Natural Inc. is recalling 998 bottles of Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief Cream due to current good manufacturing practice violations.
Pharma-Natural Inc. is recalling 1,000 jars of Dayma SUPER FORTE XL10 Pain Relieving Topical Analgesic Gel due to current good manufacturing practice violations.
Siemens is recalling seven AXIOM Artis BA X-ray systems because a power supply defect may cause the generator to fail, preventing X-ray imaging.
Abbott Laboratories is recalling 8,132 C3 in vitro diagnostic kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Abbott Laboratories is recalling 5,483 units of ARCHITECT BNP Calibrators worldwide due to a time-dependent stability drift that affects patient and control test results.
Pharma-Natural Inc. is recalling Army Health Pain Reliever Gel with Curcumin because it was manufactured with current good manufacturing practice violations.
Medela Inc is recalling 665,600 breast milk transfer lids because packaging breaches may compromise sterility, even if the packaging appears intact.
Merge Healthcare is recalling 73 units of Merge OrthoPACS software due to potential display errors in image ordering and scrolling.
Siemens is recalling five AXIOM Artis TA units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.
Siemens is recalling six AXIOM Artis BC units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.
Pharma-Natural Inc. is recalling Dermanak Skin Fade Cream because it was manufactured with current good manufacturing practice violations.
Siemens is recalling 53 AXIOM Artis dBC units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.
Siemens is recalling 98 AXIOM Artis dTC units because a power supply tolerance issue may cause generator failure, preventing X-ray imaging.
Abbott Laboratories is recalling ARCHITECT BNP Controls because of a time-dependent stability drift that affects test results.
Lupin Pharmaceuticals is recalling Nystatin and Triamcinolone Acetonide Cream due to a failed uniformity of containers test. The recall covers 33,939 tubes distributed nationwide.
Tristar Products is recalling magnetic trivets because magnets can detach and be swallowed by children, causing serious internal injuries.
Gulf Stream is recalling 2017 Serro Scotty S14 RBR travel trailers because the Federal Placard label displays an incorrect Gross Vehicle Weight Rating (GVWR).
Mazda is recalling 2019 Mazda3 vehicles with manual dimming mirrors because the mirror may detach, reducing rearward visibility and increasing crash risk.