Recent federal regulations affecting small businesses

The Commerce Department rescinds the antidumping duty administrative review for cold-drawn mechanical tubing from Switzerland for June 1, 2024 through May 31, 2025 because three named firms had no reviewable entries during the period.

Commerce rescinded antidumping and countervailing duty administrative reviews effective February 13, 2026, with a corrected period of review for boltless steel shelving imports from Taiwan.

Foreign-Trade Zone 18 seeks approval for a new subzone in San Leandro, California to serve Energy Recovery, Inc. for duty-deferred manufacturing and trade activities.

NMFS approves nine companies to provide at-sea and electronic catch monitoring services for northeast multispecies fishing sectors in 2026.

Department proposes extending an approved information collection request under the Paperwork Reduction Act without substantive changes to existing reporting requirements.

The U.S. Department of Commerce initiates antidumping and countervailing duty investigations on steel reinforcing bar imports from Mexico and Turkey to assess unfair trade practices.

New Brunswick Energy Marketing Corporation Section 206 proceeding establishes refund effective date for utility rate adjustments affecting small business energy consumers.

The Federal Council on the Arts and Humanities will convene the Arts and Artifacts International Indemnity Panel advisory committee under Federal Advisory Committee Act authority.

National Human Genome Research Institute announces amended meeting notice for stakeholder discussion of genome research funding priorities and policy updates.

Abiomed recalls 33,107 Generation 1 purge cassettes distributed worldwide in Impella Pump Sets due to increased purge leak risk that may cause serious injury or death.

Baxter Healthcare issues Class I recall of Blue Ventilator Adapter Module (Product Code M07937) for Volara Respiratory Therapy system due to risk of undetected oxygen desaturation or barotrauma in home care settings.

Medline Industries recalls 9 kits (SKUs DYKM2720, ENFITDISCKIT, and one other) with ENFit G-tube connectors that may not seal properly due to dimensional specification failures, risking leakage and requiring clinical intervention.

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.

Pocas International Corp. recalls 148 cases of popping boba ready-to-drink beverages distributed across nine US states and Canada due to packaging integrity issues that may compromise product quality.

Philips Medical Systems recalls 461 units (198 in US) of ALLURA Xper FD20 biplane X-ray systems due to wired foot switch malfunction that may prevent or intermittently disable imaging initiation.