Last Friday, the U.S. Court of Appeals for the Federal Circuit affirmed the second of the three defense verdicts in the test cases alleging that the measles-mumps-rubella vaccine causes autism. Cedillo v. Secretary, HHS, No. 2010-5004, slip op. (Fed. Cir. Aug. 27, 2010). Although the Cedillo decision turns on the specific facts of

Almost from the day this blog was founded, we’ve been arguing that class actions have no place in prescription medical product liability litigation. We’ve put up several posts containing lists of cases to that effect – but none of them were complete (or purported to be).
One of the things that we’ve often thought about

It happened in a car case, but the same thing could just as easily have occurred in litigation involving drugs or devices.
The plaintiff filed a snap motion under a peculiar Florida statute (§69.081) to have a product declared a “public hazard” and not incidentally to avoid a federal court protective order. In a kangaroo-court

We asked this morning why (1) it seemed ethical to offer into evidence an inadmissible document on the hope that opposing counsel wouldn’t object and the document would be admitted, but (2) it seemed less ethical to effect a late removal to federal court on the hope that opposing counsel wouldn’t object and the case

Many plaintiffs’ counsel prefer to litigate cases in state court.
(Film at 11!)
Thus, to avoid having product liability cases removed to federal court on the basis of diversity jurisdiction, plaintiffs sometimes include in their complaints medical malpractice claims against treating physicians. The plaintiffs and their treaters are often from the same state, which means

Sometimes it’s funny how an issue that we all know is out there sits for a long time and then, all of a sudden, it comes back at us from several different directions at once. The recent flurry of interest in the question of whether “FDA experts” – usually former FDA employees – can offer