FDA Recall Terminated

Vibe Technologies, VIBE machine, Vibrational Integrated Biophotonic Energizer.

Recall: Z-0201-2009 · Initiated October 1, 2008

Recall

Recall Number
Z-0201-2009
Event Number
49590
Firm
VIBE Technologies
FEI Number
3004494240
Status
Terminated
Root Cause
PMA
Initiated
October 1, 2008
Posted
November 3, 2008
Terminated
May 21, 2012
Address
2329 W 10th St, Greeley, CO, 80634-3527

Description

Vibe Technologies, VIBE machine, Vibrational Integrated Biophotonic Energizer.

Reason

Medical device marketed without marketing approval for claims that include cures cancer, infections, depression.

Action

Vibe Technologies notified their customers by letter on October 1, 2008 and were told to discontinue use as a medical device. This letter notification included: 1. A warning label to be placed on the Vibe machine stating that it is not a medical device and should not be used as such. 2. An updated operation manual/users guide containing no medical conditions or human body claims. 3. A certification to be signed by the user and returned acknowledging that they: received the letter; affixed the warning label to the Vibe machine; understand that the Vibe machine does not affect the structure/function of the human or animal body; will not promote the Vibe machine as a medical device; will remove any medical claims from their website; destroy any Vibe literature making medical claims. Approximately three weeks after the certified mailing, the firm will begin performing recall effectiveness checks.

Distribution

Worldwide

Quantity

851 units