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The creator of the Labradoodle cross-breed has said he inadvertently unleashed a "Frankenstein('s) monster."Wally Conron, 90, who worked for Guide Dogs Victoria in Australia when he bred the first Labrador-Poodle cross in 1989, spoke of his regrets at having begun a trend for designer breeds on an ABC podcast."I opened a Pandora's box and released a Frankenstein('s) monster," he said.His "big regret" is that his invention paved the way for "unethical, ruthless people" to breed the dogs without thinking of the health of their offspring.According to Conron, the majority of Labradoodles are "either crazy or have a hereditary problem," with healthy examples of the breed "few and far between."He believes that people have now gone too far with cross-breeding, which can increase a dog's risk of congenital disease, particularly down the generations. On the podcast, he laid particular scorn on the new Rottweiler-Poodle hybrid, known as a Rottle or a Rottie-Poo.Conron's original purpose in crossing a Labrador with a standard Poodle (which has a non-shedding coat) had been to provide a guide dog for a blind woman in Hawaii whose husband was allergic to dogs.The resulting litter of three was small, but one of the puppies did not trigger the husband's allergies and was sent to Hawaii to be her guide dog.As no one wanted the two remaining puppies, Conron asked the PR department at his work to spread the message of this new breed. Labradoodles quickly became popular in Australia and further afield.Now, designer breeds have become widespread -- but so has criticism of the consequences. Labradoodles, for example, can develop health problems common to Labrador Retrievers and Poodles such as hip dysplasia and eye disease.Colin Tennant, a British expert on dog behaviour with 45 years of experience in the industry, told CNN: "In essence, you are blindly breeding and altering genetics of the line without foreknowledge."Although Tennant said he doesn't have a problem with cross-breeding in general, he noted that breeders should pay more attention to dog's health.One example, he said, was the Bichon Frise, whose eyes water. "It must be in agony all the time," he explained. "They breed the face flat so they look humanoid because we find that attractive, with no consideration for the permutations we are producing with regards the dog's welfare or health." 2383

The American Academy of Pediatrics is calling on the U.S. Consumer Product Safety Commission to immediately recall the Fisher-Price Rock 'n Play after it has been tied to at least 32 sleep-related infant deaths. A new analysis by Consumer Reports, published on April 8, has tied 32 infant deaths to the rocker. This comes after it was tied to AAP says the previous warning did not go far enough to ensure safety and protect infants. That warning asked parents to stop using the product when the infant reaches 3 months of age or is capable of rolling over. The new Consumer Reports analysis concluded that the 32 deaths, which took place between 2011 and 2018, included babies that were less than 3-months old. The cause of death listed for some of the babies was asphyxia, or the inability to breathe caused by the babies’ position. “This product is deadly and should be recalled immediately,” said Kyle Yasuda, MD, FAAP, president of the American Academy of Pediatrics. “When parents purchase a product for their baby or child, many assume that if it’s being sold in a store, it must be safe to use. Tragically, that is not the case. There is convincing evidence that the Rock ‘n Play inclined sleeper puts infants’ lives at risk, and CPSC must step up and take immediate action to remove it from stores and prevent further tragedies.” AAP is urging parents of children of all ages to stop using the product immediately. They say stores should remove the rocker from their shelves. “We cannot put any more children’s lives at risk by keeping these dangerous products on the shelves,” said Rachel Moon, MD, FAAP, chair of the AAP Task Force on SIDS. “The Rock ‘n Play inclined sleeper should be removed from the market immediately. It does not meet the AAP’s recommendations for a safe sleep environment for any baby. Infants should always sleep on their back, on a separate, flat and firm sleep surface without any bumpers or bedding.” 1949

The CDC announced on Thursday that cigarette smoking rates in the United States have reached recorded lows with just 13.7 percent of the adult population smoking cigarettes in 2018. The percentage of smokers is just one-third from the number of smokers from 50 years ago. The CDC said that 19.7 percent of American adults used tobacco products in 2018. Cigars are used by 3.9 percent of adults; e-cigarettes by 3.2 percent of adults; smokeless tobacco by 2.4 percent of adults; and pipes, water pipes, or hookahs by 1 percent. The CDC said nearly 18.8 percent of tobacco users use two or more products. “This marked decline in cigarette smoking is the achievement of a consistent and coordinated effort by the public health community and our many partners,” said CDC Director Robert R. Redfield, M.D. “Yet, our work is far from over. The health benefits of quitting smoking are significant, and we are committed to educating Americans about the steps they can take to become tobacco-free.”While overall tobacco use has declined, e-cigarette use is on the rise, especially among young adults. More than 7 percent of young adults (ages 18-24) use e-cigarettes. According to the CDC, cigarette smoking is responsible for more than 480,000 deaths per year including more than 41,000 deaths resulting from secondhand smoke exposure. 1339

The Food and Drug Administration has announced a recall of Drospirenone and Ethinyl Estradiol tablets that may have missing or incorrect tablet arrangement.That's birth control, and the announcement says the patient taking these pills might not get the correct dosage if consumed according to the packaging."To date, no case has been reported for pregnancy and adverse event to Apotex," the recall says."Patients who have received impacted lots of Drospirenone and Ethinyl Estradiol Tablets, USP 3MG/0.03MG. or have questions regarding this recall please contact your pharmacy. Individuals should not interrupt their therapy, use a non-hormonal method of birth control, contact their health care provider for medical advice and may return the impacted packages to their pharmacist."Drospirenone and Ethinyl Estradiol Tablets, USP are an estrogen/progestin COC indicated for use by women to prevent pregnancy. Drospirenone and ethinyl estradiol tablets (inner carton) consists of 28 film-coated, biconvex tablets in the following order: 21 yellow color tablets, each containing 3 mg drospirenone (DRSP) and 0.03 mg ethinyl estradiol (EE), and 7 placebo white color tablets."These birth control pills were distributed nationwide to wholesalers and distributors. Patients should consult their doctors. Distributors are asked to return affected products to the place of purchase.Customers who purchased the impacted product directly from Apotex may call GENCO at 1(877) 674-2082 to arrange for their return.Consumers with questions regarding this recall can contact Apotex corp. by phone-number (800) 706-5575or email 1626

The New York attorney general's office issued subpoenas on Monday to two banks for records relating to the funding of several Trump Organization projects, 167

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