Federal regulations

FTC consent order against TruHeight settles allegations of unfair or deceptive practices under federal law, with terms detailed for public comment.

Tornier HRS Max tuberosity body components (233 units) are subject to a Class II recall due to incorrect labeling causing incompatibility with the HRS Max system; affected products distributed nationwide across 32 US states.

FDA holds public meeting on expanding nonprescription drug access and requests stakeholder comments; no specific deadline or financial impact stated for small businesses.

Brahms GmbH recalls Class II diagnostic test catalog 859075N due to out-of-range quality control values that may produce falsely elevated results if not properly troubleshot per instructions.

Cboe Exchange amends rules to permit options on the Dow Jones Industrial Average Index to be settled in the afternoon instead of at market close.

Molded Products Inc. voluntarily recalls 26,900 units of MPC-130 See Luer Cap Set nationwide due to threaded sleeve detachment risk, classified as Class II medical device recall.

DoD publishes unclassified notification of an arms sale transaction.

Spacelabs Healthcare recalls 1,790 multi-parameter command modules (Model 91496) due to circuit board defects that may cause inaccurate cardiac output measurements and delayed patient care.

Beckman Coulter recalls 3 boxes of MicroScan Neg Multidrug Resistant MIC test panels distributed to Poland due to manufacturing defects that may cause incorrect in vitro diagnostic results.

Connecticut Crab Company LLC recalls approximately 175 pounds of crab cakes distributed to food service in New York and New Jersey due to potential temperature abuse and botulism risk.

Department of Defense publishes unclassified text of arms sales notification for public review.

Department of Defense publishes unclassified arms sales notification to Congress as required by law.

This IFR amendment updates minimum and maximum en route altitudes and changeover points on Federal airways and jet routes to reflect National Airspace System changes and ensure safe instrument flight operations.

FDA draft guidance recommends next-generation sequencing methods for nonclinical safety assessment of investigational human genome editing products in gene therapy.

Department of Justice Office on Violence Against Women requests OMB approval to extend an information collection under the Paperwork Reduction Act of 1995; public comments accepted electronically.