Federal regulations

U.S. Department of Commerce preliminarily finds Malaysian mattress manufacturers sold below normal value during May 1, 2024–April 30, 2025, and rescinds review for companies with no subject merchandise entries.

GE Healthcare Ireland Limited recalls 306,810 vials of Omnipaque (iohexol) injection nationwide due to particulate matter that may cause temporary or reversible health problems.

Cipla USA recalls Lanreotide Injection 120 mg/0.5 mL nationwide due to sterility assurance deficiencies at the contract manufacturer's visual inspection procedure.

Viatris recalls Xanax XR 3 mg alprazolam extended-release tablets nationwide due to failed dissolution specifications that may cause temporary or reversible health problems.

Preferred Pharmaceuticals recalls 720 nationwide bottles of Geri-Care artificial tears lubricant eye drops due to lack of sterility assurance, classified as a Class II recall posing temporary or reversible health risks.

XTANT Medical recalls 2 units of Xpress Pedicle Screw System (Part X073-6555-DL) in Oregon due to mislabeling that misidentifies screw length, a Class II issue causing potential temporary health complications.

The U.S. Department of Commerce preliminarily determines countervailable subsidies were provided to certain Chinese aluminum extrusion producers and exporters during January 1–December 31, 2024, and invites interested party comments on the findings.

Department seeks public comment on revisions to foreign gifts and contracts disclosure information collection requirements under the Paperwork Reduction Act of 1995.

Teva Pharmaceuticals USA recalls 62,136 cartons of Clonidine Transdermal System and two other products due to unapproved raw material use; Class II recall distributed within the U.S.

Fagron Compounding Services recalls 16,130 bags of vancomycin HCI and four other sterile products nationwide due to failed sterility assurance and potential port detachment risks.

Stryker Sustainability Solutions recalls 56,740 tourniquet cuffs nationwide due to potential detachment at welding connections that could compromise pressure maintenance.

Siemens Medical Solutions ARTIS pheno and ARTIS Icono biplane X-ray systems (models 10849000, 11327600, 11328100, 11327700) are subject to a Class II recall due to sporadic display errors showing incorrectly elevated dose readings during patient exa…

Teva Pharmaceuticals recalls 8,376 packages of Isotretinoin Capsules due to superpotent and subpotent batches in Florida, Ohio, Puerto Rico, and Mississippi.

U.S. Commerce Department maintains countervailing duty order on citric acid and citrate salts from China, finding that revocation would likely result in continuation or recurrence of countervailable subsidies.

Beckman Coulter recalls 688 boxes of MicroScan Neg MIC 3J panels distributed in Japan due to manufacturing defects causing incorrect antibiotic concentrations in well 4/4.