State
73,106 recalls have nationwide distribution and so reach Massachusetts. 8,239 additional recalls listed Massachusetts specifically in their distribution scope.
Of the 8,239 recalls naming Massachusetts we have scored against our rubric, 1,181 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,025 (25%) are Severe.
Which agencies issued them
These figures cover only the 8,239 recalls whose distribution notice names Massachusetts specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GM is recalling certain 2023-2025 Cadillac XT5 and XT6 vehicles because the instrument panel may not illuminate when hazard warning lights, high beams or turn signals are activated.
Rivian is recalling certain 2022-2023 R1S and R1T vehicles because the maximum vehicle capacity weight value on the tire placard label is incorrect, failing FMVSS 110.
U.B.C. Food Distributors is recalling Baraka brand ground black pepper due to potential Salmonella contamination. The product is packaged in 7oz retail containers with UPC 8 22514 26626 6.
Grande Cheese Company is recalling Grande Bravo 600 Functional Whey Protein for possible Salmonella contamination. The affected product was distributed to 24 US states and to Canada, Ecuador, and Japan.
Grande Grande Primo Y45 cultured dairy product is being recalled due to possible Salmonella contamination. The product was distributed across multiple U.S. states and internationally to Canada, Ecuador, and Japan.
Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper contaminating the drug. The recall affects 2,806 vials distributed nationwide.
Grande Ultra 9150 Whey Protein Isolate (Product Code 32324) is being recalled due to possible Salmonella contamination. The affected product was distributed to 24 US states and internationally to Canada, Ecuador, and Japan.
Grande Cheese Company is recalling Grande Bravo 300 Functional Whey Protein (SKU 32102) due to possible Salmonella contamination. The affected product was distributed across multiple US states and internationally.
Grande Cheese Company is recalling Grande Ultra 8000 Nutritional Whey Protein Isolate due to possible Salmonella contamination. The affected batches include AOE813-1 through AOE813-4 and AOF840-1 through AOF840-4.
Grande Cheese Company is recalling Grande Bravo 250 Functional Whey Protein (SKU 32101) for possible Salmonella contamination. The recall affects 1,726,910 pounds distributed across 24 U.S. states and exported to Canada, Ecuador, and Japan.
The Thoratec HeartMate System Monitor is being recalled due to display malfunctions affecting 4,842 devices worldwide. These issues may prevent proper monitoring and device control.
Grande Bravo 500 Functional Whey Protein is recalled due to possible Salmonella contamination. The product was distributed across 24 US states and internationally to Canada, Ecuador, and Japan.
Mt. Capra Goat Milk Formula Recipe Kit recalled for marketing as infant formula without FDA premarket notification.
Grande Lactose (SKU 30601) is being recalled due to possible Salmonella contamination. The affected product was distributed across multiple US states and internationally.
GRANDE CHEESE COMPANY is recalling Grande Ultra 9100 Functional Whey Protein Isolate (SKU 32131) due to possible Salmonella contamination. The recall affects 1.7 million pounds distributed to 24 U.S. states and international markets.
Grande Bravo 550 Functional Whey Protein is being recalled due to possible Salmonella contamination. Affected batches ANV508-1 and ANV508-3 were distributed across 24 U.S. states and internationally.
Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper. Lot F1040001 was distributed nationwide.
Aesculap Inc is recalling Aeos Robotic Digital Microscope models with Product Code PV010 due to failure of the integrated safety mechanism. The robotic arm may drop more than 10 cm from its original position after the emergency stop button is pressed.
Rygel Advanced Machines recalls OMTech Desktop Laser Engravers due to missing safety interlocks and labeling. The devices lack required redundant interlocks and certification labels that prevent accidental laser exposure.
Porsche is recalling certain 2020–2025 Taycan vehicles because the front brake hoses can develop cracks and leak brake fluid, reducing braking performance. Dealers will replace the hoses for free.
Covidien is recalling EsoFLIP 30mm balloon dilation catheters due to saline conductivity issues that may cause inaccurate esophageal measurements, potentially leading to patient harm.
Integra LifeSciences is recalling CODMAN BACTISEAL EVD catheters due to external packaging seal defects that may compromise sterility. The recall affects 59 units distributed internationally.
Winder Laboratories is recalling Phenazopyridine HCl tablets (Lot #1142404) due to a product mix-up where some bottles contain Phenobarbital tablets instead. No illnesses or injuries have been reported.
B Braun Medical Inc is recalling over 1.1 million Stimuplex A nerve block needles labeled as DEHP-free, but the adhesive contains traces of DEHP. The mislabeling poses a risk to users who selected the product specifically to avoid DEHP exposure.
Ortho-Clinical Diagnostics is recalling VITROS Anti HBs Calibrators due to potential for positively biased results caused by signal reduction over shelf life. Approximately 481 units were distributed worldwide.