State
72,820 recalls have nationwide distribution and so reach DC. 2,795 additional recalls listed District of Columbia specifically in their distribution scope.
Of the 2,795 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 946 (34%) are Severe.
Which agencies issued them
These figures cover only the 2,795 recalls whose distribution notice names District of Columbia specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Siemens Healthcare Diagnostics is recalling specific lots of the Emit 2000 Quinidine Assay because unacceptable precision may cause falsely high results, risking improper patient treatment.
American Regent, Inc. is recalling Selenious Acid Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling Acetylcysteine Solution USP due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling specific lots of Acetylcysteine Solution, USP, 10% due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Philips is recalling 1,810 Cardiac Workstation 7000 units because they may intermittently provide inaccurate native heart rate data.
Boston Scientific is recalling ENROUTE Transcarotid Neuroprotection Systems due to a potential for arterial sheath tip separation or partial tip separation during use.
Arrowhead DE LLC is recalling 4,171 Arrow-LOK Implants because they did not undergo a required gamma radiation dose audit, which could reduce sterility assurance and lead to patient infection.
Boston Scientific is recalling ENROUTE Transcarotid Neuroprotection System Plus catheters due to a potential for arterial sheath tip separation during use.
Lidl US is recalling Vitasia Asian Style Wok Spice Mix because a positive test result detected Salmonella in the product.
Intersurgical Inc is recalling 21,269 One-Piece Guedel Airway devices because they may be occluded or partially occluded. The devices were distributed in six US states.
Siemens Healthineers is recalling 24 units of the Immulite 2000 Syphilis Screen assay due to a potential negative patient bias that may report low reactive results as nonreactive.
Boston Scientific is recalling Suture Cinch Long endoscopic tissue approximation devices because they may fail to deploy the implant or cut the suture.
Beckman Coulter is recalling DxC 500i Clinical Analyzer Modules due to a software defect that may cause erroneous patient test results.
Fort Defiance Industries is recalling Automated Field Steam Sterilizers because a water recovery system connector may lose ground continuity, creating an unreliable fault current return path.
Philips is recalling 796 Cardiac Workstation 5000 units worldwide because they may intermittently provide inaccurate native heart rate data.
Intersurgical Inc is recalling 1,575 One-Piece Guedel Airway devices because they could potentially be occluded or partially occluded.
Maquet Critical Care AB is recalling nine Y Sensor Modules for the SERVO-U/-N ventilator systems because they did not undergo required electrical safety and functional tests during production.
restor3d Inc. is recalling 59 Veritas Standard Glenoid Baseplates because incorrect machining of peripheral screw holes may cause improper screw engagement.
Sun Pharmaceutical Industries is recalling 1,968 bottles of Carbamazepine 200mg tablets due to CGMP deviations and black spots found on tablets.
Beckman Coulter is recalling DxC 500 AU Clinical Analyzer Modules due to a software defect that may cause erroneous patient test results.
ConvaTec is recalling Esteem Body Soft Convex Urostomy Pouches because they may leak from the cap during use.
Boston Scientific is recalling OverStitch Suture Cinch devices because they may fail to deploy the implant or cut the suture as intended.
Gentherm Medical is recalling 46 Innercool Coolblue Console units because overheating of the 115V CPU board may cause the device to shut down.
Siemens Healthineers is recalling Immulite 2000 Syphilis Screen assays because a negative patient bias may cause low reactive results to be reported as nonreactive.
Bell Sports is recalling specific Pit Boss helmets that may lack proper impact protection, increasing injury risk in crashes.