Archive for July, 2009

Riegel At 1 1/2 : What Do We Know Now About Parallel Violation Claims?

Thursday, July 30th, 2009

Our last preemption-related post was more than three weeks ago, on July 2. Can you believe it? What ever happened to “all preemption, all the time,” as we used to be called?

The Supreme Court decided all of its pending cases, that’s what. Device preemption is pretty much settled, unless Congress upsets the applecart. Drug preemption is in a bit of a hiatus as appellate courts digest Levine and have yet to rule (more…)

Compounding, Repackaging, or Manufacturing?

Thursday, July 30th, 2009

We don’t deal with FDA regulatory matters that often, and with the criminal side even less, but the recent decision out of Colorado in U.S. v. Bader, slip opinion here, was too juicy to ignore.

It points out a serious flaw in the FDA’s regulatory scheme that we think needs a formal regulatory fix – and soon.

The issue in Bader is the limits on pharmacy compounding.

In Bader a pharmacist (more…)

Does Neurontin Make You Scratch Your Head?

Wednesday, July 29th, 2009

Plaintiffs say that Pfizer’s anti-epileptic drug, Neurontin, causes people to commit suicide.

We say that it makes you scratch your head.

The first Neurontin-suicide case went to trial earlier this week. It sounded like a tough case for plaintiff: The decedent, who had taken Neurontin and then committed suicide, had a history of mental health disorders and abusing drugs, including cocaine. (Here’s a link to a Bloomberg story (more…)

Removal Based On Misjoinder Of A Treating Physician

Sunday, July 26th, 2009

We’ve published a couple of posts recently (here and here) about removal in the tough context — where the medical malpractice and product liability claims arise out of the same medical treatment. In that situation, the removing product manufacturer must convince the federal court to sever (and remand) the malpractice claims, and to retain jurisdiction over the product liability claims, even though evidence introduced at the malpractice and products (more…)

Going Our Way? Class Actions, Punitive Damages & Due Process

Tuesday, July 21st, 2009

Since the Supreme Court handed down Philip Morris USA v. Williams, 549 U.S. 346 (2007), we’ve posted twice – here and here – that we think Williams’ reaffirmation, in the specific context of punitive damages, of defendants’ rights to maintain all available legal defenses sounds the death knell for punitive damages class actions.

And not just in the blogosphere. One of us took this constitutional (more…)

A Trot Through Some Recent Scholarship

Tuesday, July 21st, 2009

We’re kicking back today and letting others do the work for us.

Generally, practitioners don’t read the law reviews. So we’re skimming the tables of contents for you.

Today’s post simply describes four recent scholarly articles — two on preemption, one on post-sale duties to warn, and one theorizing about how tort law should be coordinated with non-tort regulatory standards — that may tickle your fancy.

If none (more…)

Dr. Strangelove Redux

Monday, July 20th, 2009

Remember “Dr. Strangelove”?

“Ripper: Have you ever heard of a thing called fluoridation. Fluoridation of water?

Mandrake: Uh? Yes, I-I have heard of that, Jack, yes. Yes.

Ripper: Well, do you know what it is?

Mandrake: No, no I don’t know what it is, no.

Ripper: Do you realize that fluoridation is the most monstrously conceived and dangerous Communist plot we have ever had to face?”

(more…)

Taking Stock

Friday, July 10th, 2009

The two of us have been practicing law now for a little over 25 years. Bexis graduated law school in 1982 and Herrmann a year later (see our bios – links at the top – for the gory details). At big firms it takes a few years – five at least – before we could start to have any real strategic impact on the cases we were working on. And it took a few years for us to get around to being product liability defense lawyers in the first place.
(more…)

ADE Reports: Redaction Required

Thursday, July 9th, 2009

Yes, Virginia, the FDA’s regulations requiring redaction of physician identifying information from Adverse Drug Event (”ADE”) reports are mandatory – even if plaintiffs obtain them … well … irregularly.

That’s the lesson of a brand new discovery decision in In Re Mentor Corp. Obtape Transobturator Sling Products Liability Litigation, 4:08-MD-2004, slip op. (M.D. Ga. July 10, 2009), decided earlier today.

Here’s (more…)

Daubert Gives Plaintiffs A Pain In The Pump

Tuesday, July 7th, 2009

Last year, the MDL Panel denied an attempt to centralize all of the federal “shoulder pain pump – chondrolysis” cases. See In re Shoulder Pain Pump – Chondrolysis Products Liability Litigation, MDL No. 1966 (JPML Aug. 11, 2008) (link here). So the cases have moved ahead individually in federal courts across America.

A couple of weeks ago, a defendant got good news in one of those cases. In Kilpatrick v. Breg,Inc., No. 08-10052-CIV-MOORE/SIMONTON, (more…)