State
72,940 recalls have nationwide distribution and so reach Massachusetts. 8,209 additional recalls listed Massachusetts specifically in their distribution scope.
Of the 8,209 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 2,013 (25%) are Severe.
Which agencies issued them
These figures cover only the 8,209 recalls whose distribution notice names Massachusetts specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ambriola is recalling 2,106 units of Boar's Head Grated Pecorino Romano in 6 oz cups after the product tested positive for Listeria monocytogenes.
Ambriola is recalling 184 units of Locatelli Grated Pecorino Romano 48/8oz shippers after the product tested positive for Listeria monocytogenes.
Ambriola is recalling 1,015 bags of Sam's Pecorino Romano grated, 1.5 lb, after the product tested positive for Listeria monocytogenes.
Ambriola is recalling 45 bags of Pinna Grated Pecorino Romano in 10-pound sizes after the product tested positive for Listeria monocytogenes.
South Asian Food is recalling 95 boxes of Bengal King Jhal Chanachur food treats because the product contains undeclared peanuts. The FDA has classified the action as Class I.
AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
Ambriola is recalling 964 bags of Locatelli Grated Pecorino Romano in 5 and 10-pound sizes after the product tested positive for Listeria monocytogenes.
MediNatura is recalling all lots within expiry of ClearLife Allergy Nasal Spray, Extra Strength, after the products were found to contain yeast, mold and Achromobacter.
CareFusion 303 is recalling 2,079 BD Pyxis ES Enterprise Server systems over a software issue that may result in equipment not receiving timely updates of patient or medication information.
Securitas Healthcare is recalling 5,627 Arial 900 MHz Call Stations, model CSK200-900, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.
Imprimis NJOF is recalling 596 boxes containing 11,920 pre-filled syringes of Dexamethasone, Moxifloxacin and Ketorolac intraocular injection over glass-like particles.
Imprimis NJOF is recalling 314 boxes containing 6,280 pre-filled syringes of Tri-Moxi triamcinolone and moxifloxacin intraocular injection over glass-like particles.
Direct Source Seafood is recalling 1,800 cases of waterfront BISTRO frozen raw shrimp, sold alongside Market 32 brand shrimp, because the shrimp may be contaminated with Cesium-137.
Town Food Service Equipment is recalling approximately 11,300 aluminum sauce pans in 1QT to 3QT sizes after the product was found to contain leachable lead levels.
Direct Source Seafood is recalling 3,290 cases of Market 32 by Price Chopper frozen raw shrimp because the shrimp may be contaminated with Cesium-137.
MAYEJ Comercializadora is recalling 1,288 boxes of Italian Parsley over the pathogen Cyclospora cayetanensis.
Imprimis NJOF is recalling 778 boxes containing 15,540 pre-filled syringes of Dexamethasone and Moxifloxacin intraocular injection over glass-like particles.
Remote Diagnostic Technologies is recalling 7,129 Philips Tempus Pro Patient Monitors because intracranial and bladder pressure measurements have not been tested or validated for accuracy.
Roche Diagnostics is recalling 1,300 Elecsys Anti-TSHR cassettes because results vary by instrument platform and calibrator lots vary, which may lead to incorrect diagnosis or treatment.
IMRIS Imaging is recalling 122 HFD100 Head Fixation Devices because a torque screw may crack or separate, which could lead to inadequate head stabilization and risk of patient injury.
Securitas Healthcare is recalling 1,898 Arial 900 MHz Call Stations, model CSK200-900MR, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.
Meridian Bioscience is recalling 211 units of the Revogene C. difficile assay because affected lots show a decline in performance over time, which may lead to false-negative results.
Philips North America is recalling 13,470 Smart-hopping 2.0 AP 1.4 GHz patient monitors because the MX40 could not reconnect to the PIC iX when signal strength changed quickly.
Medline is recalling 1,611,081 Hudson RCI medium concentration oxygen masks after multiple complaints of tubing disconnecting, which may lead to shortness of breath and hypoxia.
Rovira Biscuit is recalling 16,478 units of Great Value Vainilla Crackers over undeclared colours FD&C Yellow #6 and FD&C Red 40.