Shoulderflex massager recall
Splet18. nov. 2011 · At that time, the U.S. Food & Drug Administration (FDA) announced that the ShoulderFlex Massager was associated with at least one death and one near-strangulation. Now, the FDA has deemed the recall that was initiated on August 30, 2011 as a Class I recall, its most serious. Class 1 recalls involve situations in which there is a reasonable ... Splet17. nov. 2011 · ShoulderFlex personal massager recall upgraded to Class I. November 17, 2011 By MassDevice staff. The FDA upgraded personal massage device maker King …
Shoulderflex massager recall
Did you know?
http://healthnewsdigest.com/2011/12/21/do-not-use-shoulderflex-massagers/ Splet19. dec. 2011 · Recall Class: Class I Date Recall Initiated: August 30, 2011 Product: ShoulderFlex Deep-kneading Shiatsu Massager, Model # SH61 This product was manufactured from June 1, 2003 through January 27, 2011 and distributed from October 18, 2003 through April 19, 2011. See related Safety Communication and Firm Press Release …
Splet02. sep. 2011 · On Wednesday, King International recalled about 12,000 ShoulderFlex massagers that had been sold nationwide over the past eight years. The FDA said there … Splet15. sep. 2011 · The FDA is also requesting that consumers separate the parts of the massager by removing the massage fingers and the power supply and discard them separately to prevent it from being reassembled. On August 31, 2011, King International announced a recall of its ShoulderFlex Massager.
Splet26. avg. 2011 · BACKGROUND: The ShoulderFlex Massager is a personal massage device sold in retail stores, catalogs and over the Internet. It is intended to provide users with a deep tissue massage to the neck, shoulders and back area while lying down. ... King International has not followed through with recall procedures; the 800 number … Splet21. dec. 2011 · Consumers are being warned again about possible strangulation from using the ShoulderFlex Massager after the now defunct importer failed to follow through on its recall, the U.S. Food and Drug ...
Splet02. sep. 2011 · The Shoulderflex massager recall was announced on August 31 by the manufacturer, King International LLC, after the FDA urged consumers last week not to …
Splet#ShoulderFlex Massager linked to serious injury risk, strangulation or death by FDA http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm269721.htm reservation registers and roster registersSplet26. avg. 2011 · The ShoulderFlex Massager, say federal regulators, can be lethal. ... Exclusive Deals for Members Best Time to Buy Products Recall & Safety Alerts TV Screen … reservation rennesSplet21. dec. 2011 · (Reuters) - Consumers are being warned again about possible strangulation from using the ShoulderFlex Massager after the now defunct importer failed to follow … prostate shave surgerySplet28. avg. 2011 · The FDA is currently evaluating manufacturer King International's plan for a recall of the ShoulderFlex Massager. The personal massage unit is made up of a rotating bar that a patient places on a ... prostate severity scoreSplet28. dec. 2011 · According to news sources, The Food and Drug Administration is reminding consumers not to use the ShoulderFlex Massager that was recalled Aug. 31, 2011 due to strangulation hazards. The manufacturing company, King International, has been out of business since the recall of its ShoulderFlex Massager product went into place. The … reservation remote jobsSplet30. avg. 2011 · To date, some 12,000 ShoulderFlex massagers have been sold. The FDA now warns that owners should dispose of their machines. The manufacturer is also being … reservation repas kermesseSplet19. sep. 2011 · The federal government’s Food and Drug Administration announced recently that Beaverton-based King International has agreed to recall its ShoulderFlex Massager. The Oregon product recall was ordered after evidence emerged that ShoulderFlex use can lead to serious injuries or even a product liability-related Oregon wrongful death. reservation request form sgip