Approximately 4 million packages of Children's Benadryl Allergy Fastmelt
Tablets (grape and cherry flavors) and 800,000 bottles of Motrin
Junior-Strength have been recalled by Johnson & Johnson (J&J).
Consumers can continue using their products because the recall refers to
the wholesale and retail part of the distribution process only.
The recalled Benadryl was distributed to the USA, Canada, Barbados, Belize, St. Martin, St. Thomas and Puerto Rico, while the Motrin was only distributed inside the USA.
According to J&J, there were issues at the Fort Washington, Pennsylvania plant which has since closed. The packaging of said products appears to be fine, however, an internal review detected "insufficiencies in the development of the manufacturing process."
2010 has been a bad year for J&J recalls. In late April, over 135 million bottles of OTC medicines were recalled due to manufacturing deficiencies, included in the recall were Tylenol, Motrin, Zyrtec and Benadryl.
J&J recalls eventually triggered an FDA (Food and Drug Administration) investigation. The FDA wrote an extremely critical report about manufacturing practices at the J&J's McNeil Consumer Healthcare Unit (plant) at Fort Washington. There were two Senate investigations. An Oversight Committee hearing revealed some unusual cover-ups.
McNeil Consumer Healthcare spokesperson, Bonnie Jacobs, said:
The recalled Benadryl was distributed to the USA, Canada, Barbados, Belize, St. Martin, St. Thomas and Puerto Rico, while the Motrin was only distributed inside the USA.
According to J&J, there were issues at the Fort Washington, Pennsylvania plant which has since closed. The packaging of said products appears to be fine, however, an internal review detected "insufficiencies in the development of the manufacturing process."
2010 has been a bad year for J&J recalls. In late April, over 135 million bottles of OTC medicines were recalled due to manufacturing deficiencies, included in the recall were Tylenol, Motrin, Zyrtec and Benadryl.
J&J recalls eventually triggered an FDA (Food and Drug Administration) investigation. The FDA wrote an extremely critical report about manufacturing practices at the J&J's McNeil Consumer Healthcare Unit (plant) at Fort Washington. There were two Senate investigations. An Oversight Committee hearing revealed some unusual cover-ups.
McNeil Consumer Healthcare spokesperson, Bonnie Jacobs, said:
- "There's no safety issue, and consumers don't have to take any
action. There's no indication the products don't meet quality standards,
and it's not being undertaken on the basis of adverse events."
1 comment:
oZzy moved away a few months ago, I miss his cock, that i'm always hungry for sexual intercourse.
FUCK MY PUSSY!
My page; hcg injections
Also see my web page > hcg injections
Post a Comment