[Granville-Hough] 4 Apr 2009 - Blue Language And the Jakewalk Blues, 3rd part
Trustees for Granville W. Hough
gwhough-trust at oakapple.net
Tue Apr 4 05:56:04 PDT 2017
Date: Sat, 04 Apr 2009 05:35:18 -0800
From: Granville W Hough <gwhough at oakapple.net>
Subject: Blue Language And the Jakewalk Blues, 3rd part - 4 April 2009.
In considering the way the judges and lawyers in Boston handled this
case, one must conclude that the judge was a victim of astounding
ignorance, and/or mistrust of government agencies from Washington, DC,
or susceptible to bribery or other coercion. There is little doubt
that, today, US firms trading in arms, chemical stocks, and raw drugs
are so influential that they make a mockery of any effort to suppress
illegal drug trafficking. The question before us is this: Would
legalizing drugs improve the situation? If we say YES, then how would
we go about it?
Another form of paralysis was associated with moonshine, and I
will talk about it tomorrow.
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(Harold Hopkins, continued)
FDA's chief of drug control, J. J. Durrett, made an investigative
swing through the South where some of the lagrest outbreaks of Jakeleg
had occurred. Upon returning, Durrett wrote to the chief of FDA's
Eastern District about watching an experiment in New Orleans in which a
pig was paralyzed when given some of the poisoned jake. And he
addedddd: "We cannot escape the impression that somewhere around the Hub
Products Co. and its products the answer (to the cause of the poisoning)
is to be found."
It was. While Durrett was urging the prompt collection of samples
of the poisoned jake to build a case against Hub, the chief of FDA's New
York Station, Joseph Callaway Jr., reported to Washington that his
laboratories had extracted from a jake sample "an oily residue
resembling phenol." Before 1930 was out that "oily residue" had been
identified by other Government chemists as the poisonous substance
triorthocresyl phosphate.
By mid-summer Federal grand juries in several cities had returned
indictments against Hub's principals -- Harry Gross, President, and Max
Reisman, his brother-in-law and part owner. When FDA investigators went
to the Hub plant at 65 Fulton Street, Boston, Gross refused permission
for them to inspect it and told them to return the next day. They did,
but samples given them contained no unusual substances. Hub Products
closed down its operations immediately. Investigators of the
Prohibition Agency and FDA made seizures in a number of cities, but too
often in tracing shipments from Hub to distributors they found that the
evidence had already been drunk. Enough of the poisoned product were
intercepted in various cities, however, to weave together a strong web
of evidence implicating Hub Products.
In February 1931, the several cases pending against Gross and
Reisman were consolidated for trial in Boston, and the two men were
charged with conspiracy to violate, and with violations of the National
Prohibition Act's prohibition against selling jake as an alcoholic
beverage and of the adulteration and misbranding provisions of the Food
and Drugs Act of 1906. Both men pleaded guilty. The two men were
sentenced to 2 years imprisonment and fined $1,000 each. However, the
jail sentence was suspended and both were placed on probation for 2
years. FDA men, who had worked so hard to bring the cases to court,
were stunned. The light sentences were later said to have been given in
a plea bargaining arrangement under which the defendants were to present
evidence that would convict the "real" culprits, the New York
bootleggers from whom Gross claimed he got all his products..
As a result of this arrangement, Gross and Reisman and their lawyers
met and conferred in Mid-May of 1931 with Haven Parker, assistant U. S.
Attorney in Boston, but the information they offered was nebulous and
insubstantial. The New York culprits had evaporated.
FDA was particularly miffed becaused it representatives were not
asked to this conference. On May 31, 1931, George H. Adams, chief of
FDA's Boston Station reported evidence to headquarters that traced the
sale of 135 gallons of triothoocresyl phosphate to Hub Products Co.
Under the trade name Lyndol -- a plasticizer manufactured by the
Celluloid Co., Newark, N. J. and used as an ingredient in lacquers and
othe chemical products -- this chemical had been sold to Hub by a
chemical products broker, Raffi and Swanson, Boston. This was enough
triorthocresy phosphate to adulterate 200 barrels of jake or 640,000
2-oz. bottles.
The failure of the conference with Gross and Reisman to provide
solid evidence against the New York bootleggers they claimed were
responsible for the poisoned jake strengthened the FDA's determination
to find the source of the contamination. Trials had been held in New
York and elsewhere and a number of people convicted of selling the
poisoned product, but evidence of who performed the original
adulteration was not established.
After conducting its own investigation in New York, FDA concluded
that both Gross and Reisman were lying about the origins of the
poisoning and thus had violated the terms of their probation. The
Agency decided to probe further in Boston.
George White, a former employee at Hub, told investigators that he
had received the barrels of Lydol, left them on the third floor of the
Hub premises, where they were removed to the fourth floor by Gross and
the empty containers returned afterward. White said he had no access to
the fourth floor, which was kept locked at all times, and that Hub's
goods apparently were shipped out at night because he would see them
near the elevator on the third floor when he left for the day and they
would be gone when he returned in the morning. Adams presented this
information to the U.S. Attorney.
On April 1 1932, Gross was charged with violating probation and
ordered to serve his 2-year prison term. Later Judge James A. Lowell
refused to hear the Government's case asking revocation of Reisman's
probation.
Other charges of selling poisoned jake had been brought against
Gross and Hub Products in December 1931 and had been tried January 25
1932. The defendants pleaded guilty and the only sentence was a fine of
$1, Judge Lowell explaining that these cases should be considered a part
of the earlier ones, for which the defendants had already been punished.
The jake poisoning events of 1930 showed plainly that legislation
was needed to require premarket testing to assure the safety of drugs
sold in the United States. The strongest charges that could be brought
against the men responsible for so many deaths and permanent cripplings
were that they conspired to ship and had shipped large quantities of
adulterated and misbranded drugs "consisting of approximately 1,000
gallons of a product called 'fluid extract of ginger,' and sometimes
called 'Liquid Medicine in Bulk,' which differed from the standard of
strength, quality, and purity as determined by the tests laid down by
the United States Pharmacopoeia for fluid extract of ginger."
Some observers of the widespread Jakeleg epidemic of 1930 considered
it more joke than jake, and in a way it was, a grim and lasting
reminder of the country's noble, adventurous, and sometimes hilarious
dozen years with legally imposed temperance. When the Nation was voting
to go dry in 1818, my father was in France and had no say in the
matter. But the notion didn't set well with him and he had no intention
whatever of letting the agents respoonsible for enforcing Prohibition
deter him from taking a drink, if he could find one. Just 3 years shy
of Repeal, when happy days were just ahead, he and 35,000 other revelers
found one drink too many.
Harold Hopkins is editorial director of _FDA Consumer.
/From _FDA Consumer, _June 1980.
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