State
72,919 recalls have nationwide distribution and so reach Massachusetts. 8,208 additional recalls listed Massachusetts specifically in their distribution scope.
Of the 8,208 recalls naming Massachusetts we have scored against our rubric, 1,171 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,012 (25%) are Severe.
Which agencies issued them
These figures cover only the 8,208 recalls whose distribution notice names Massachusetts specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Windstone Medical Packaging is recalling Custom Convenience Kits Pre Op Kits (Part Number AMS14994A) due to a potential for backflow of medication from secondary IV containers into primary IV containers. The recall affects 520 units distributed nationwide.
FDA has rescinded 510(k) regulatory clearances for certain Control Syringes, Guidewires, and High-Pressure Tubing components in two Medline medical device kits distributed nationwide.
B. Braun Medical Inc. is recalling Lactated Ringers Irrigation 3000 mL bags due to lack of assurance of sterility and potential leakage from the diaphragm port after foil removal.
Medline is recalling convenience kits containing select 10 mL polycarbonate colored syringes because of unapproved design changes made outside the 510(k) clearance. 270,311 units are affected.
XTANT Medical Holdings is recalling nanOss 3D Advanced Bone Graft Substitute products due to incorrect labeling showing a 5-year shelf life when the approved shelf life is four years.
The Harvard Drug Group LLC is recalling Omega-3-Acid Ethyl Esters capsules (1 gram, 50-count cartons) due to failed capsule specifications discovered during routine stability testing.
Medline Industries is recalling Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance.
Olympus is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2113) because the Version 2 reprocessor connecting tube lock levers may fail prematurely. The defect could affect proper connection during endoscope reprocessing.
Magellan Diagnostics is recalling the LeadCare Ultra Blood Lead Test Kit (Catalog Number 70-8098) because use with certain third-party micro-collection devices may produce unexpectedly elevated and false positive results, potentially causing delayed diagnosis and unnecessary additional testing.
Angiodynamics is recalling Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided devices due to a manufacturing defect that may prevent guidewires from passing through the catheter hub.
SurgiSmoke Solutions is recalling certain lots of the Flamingo Funnel Large (Model SQ20012-03) surgical device due to a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.
Premier Dental Products is recalling Monsel's Solution (ferric subsulfate) 8 mL vials because the expiration date on the vial itself is printed with an extra digit (2709114 instead of 270914). The carton expiration date is correct.
Ford is recalling certain 2024-2026 Ranger and Bronco vehicles because the front seat frame height-adjust pivot bolt may be loose or dislodged. 179,698 vehicles are affected.
Lode-King is recalling 2019-2026 trailers because missing welds on the rear impact guard reduce structural strength, increasing injury risk in rear-end crashes.
Harley-Davidson is recalling certain 2024–2026 motorcycles with a potentially blocked airbox breather port that may cause crankcase pressure to build up, risking oil ejection and injury when the dipstick is removed.
Jayco is recalling 2026 Entegra Condor and Granite Ridge motorhomes because a tempering mixing valve may be missing from the water heater, creating a scalding risk.
American Battery Solutions is recalling Proliance High Voltage Batteries because a contactor may fail to close, causing a loss of drive power and increasing crash risk.
Audi is recalling certain 2025 Q5, Q5 Sportback, SQ5 and SQ5 Sportback vehicles because the driver and front passenger seat belts may have been manufactured incorrectly.
Shyft Group is recalling 2022 Utilimaster Aeromaster vehicles because the Gross Vehicle Weight Rating on the certification label may be incorrect, potentially leading to overloading.
AMZCMJ DGD is recalling its children's tower stools because they can tip over or collapse, posing risks of serious injury or death from falls and entrapment.
FitRx SmartBell Quick-Select adjustable dumbbells are recalled after more than 115 reports of weight plates dislodging during use, with at least six injuries including broken toes.
Mack Trucks is recalling 2,772 Pioneer and Anthem vehicles because unprotected electrical connectors may cause a loss of anti-lock brakes and stability control.
REV is recalling 2026 Fleetwood and Holiday Rambler motorhomes because a furnace defect may turn on the generator unexpectedly, posing a carbon monoxide risk.
32 Degrees heated socks sold at Costco are recalled after 14 heat-related incidents, 13 of them involving first- or second-degree burns. About 207,806 units are affected.
BlissfulDestiny is recalling its Magnetic Stick Figure Sets because they contain loose magnets that pose a serious injury or death risk if swallowed.