Federal regulations

Reflexion Medical RefleXion X1 Radiotherapy System Model RXM1000 Class II recall affects 12 units in California and Texas due to software defect causing potential 5mm treatment displacement and 10-20% underdose during repeat localization procedures.

Philips Respironics issues Class I recall of 113,717 Trilogy Evo O2 ventilators and related devices nationwide due to obstruction alarm delay that may take up to four breaths to trigger.

The Maros Group recalls Prickly Pear Jelly (9 oz bottles) distributed in Arizona due to undeclared milk allergen; 24 bottles affected in Class II recall.

Lone Star Dairy Products LLC recalls 1,791,543.94 lbs of spray-dried dairy powder nationwide due to salmonella contamination identified in finished product testing.

Summa Therapeutics recalls 22 units of Finesse BTK Multicath injectable angioplasty balloon catheters nationwide due to potential balloon burst specification failures posing temporary health risks.

Medline Industries recalls 420 units of sterile radiology procedure kits (model DYNDH1491B) nationwide in Minnesota due to potential sterile pouch packaging breach that may compromise product sterility.

Stryker CHROMOPHARE Softlit Ring Surgical Light System recall affects 6,170 units worldwide due to ceiling cover support deficiency posing temporary health risks.

Olympus recalls 408 SOLTIVE Premium laser systems worldwide due to a defective 24V power supply module that may render units inoperable or produce smoke and burning smells within the enclosed console.