State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GE Healthcare is recalling 526 Discovery NM 530c systems because outdated software caused a patient finger injury during an automatic unload process.
Baxter Healthcare is recalling 4,065 Gambro Cartridge Low Weight-Low Volume Blood Transport Systems due to a potential tubing disconnection hazard.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.
Cook Inc. is recalling 1,899 Pressure Monitoring Trays because excess coating material on the needle component could cause occlusion.
Island Wear is recalling about 940 umbrella strollers sold in Ocean City, Md., because they violate federal safety standards, posing fall and choking risks to children.
Cook Inc. is recalling 6,792 Pressure Monitoring Sets because excess coating material on the needle component could cause occlusion.
Agfa N.V. is recalling 13 DR 800 digital radiography systems because a software error may cause incorrect dose calculations during specific fluoroscopic exams.
Baxter Healthcare is recalling Gambro Cartridge Blood Sets due to a potential tubing disconnection hazard during hemodialysis treatment.
American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered by the FDA.
Philips is recalling 91 ProxiDiagnost N90 units because defective thermo switches may fail to power down the system, causing the transformer to overheat and generate smoke.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out post-operatively.
Hill-Rom is recalling 4,381 Centrella Smart+ Beds because the Bed Exit System may fail to send remote alerts to the nurse call system under specific conditions.
American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered with the FDA.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out after surgery.
Inpeco S.A. is recalling 71 FlexLab Augomation Systems because a firmware error may dilute primary sample tubes with distilled water, potentially causing discrepant patient results.
Osteomed, LLC is recalling 153 units of Osteovationex 3cc ImpactFormula bone void filler because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.
Osteomed, LLC is recalling 651 units of Osteovation RMX 10 CC Injectable bone void filler kits because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.
American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered by the FDA.
Olympus is recalling 18 ShockPulse-SE Lithotripsy System transducers because a component was made with non-conforming material that could allow water ingress during sterilization.
Inpeco is recalling 97 Accelerator a3600 Automation Systems because a firmware error may dilute primary samples with distilled water during clot detection.
American Contract Systems is recalling 2,868 sterile surgical packs because they were manufactured in a facility not registered with the FDA.
Teva Pharmaceuticals USA is recalling specific bottles of mixed amphetamine salts tablets because some may contain mixed strengths.
American Contract Systems is recalling sterile custom surgical packs because they were manufactured in a facility not registered by the FDA.
Philips is recalling Chest Pneumograph accessories because the labeling does not state that the product contains natural rubber latex.
Torrent Pharma Inc. is recalling 6,228 bottles of Carbamazepine 200 mg tablets because they failed to meet dissolution specifications.