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| The United States: H&P Industries, Inc. issues a voluntary nationwide recall of all lots of Povidine Iodine Prep Pads due to potential microbial contamination(English Only) |
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H&P Industries, Inc. has initiated a voluntary product recall of all lots of Povidine Iodine Prep Pads manufactured by H&P Industries, Inc. but which are private labeled for many accounts. This recall has been initiated due to results of the FDA’s ongoing investigation and sampling efforts, and H&P Industries, Inc. internal investigation. The Povidine Iodine Prep Pads are non-sterile and contain some of the same raw material as the recalled Alcohol Prep pads, and were therefore investigated by FDA and by H&P Industries for potential contamination with objectionable organisms. However, analytical testing showed the presence of objectionable organisms, namely Elizabethkingia meningoseptica.
The affected Povidine Iodine Prep Pads can be identified by the names listed below in their packaging:
Cardinal Health
Medical Specialties
VHA
Triad
Triad Plus
North Safety
Total Resources
Please refer to the following website in FDA for details:
http://www.fda.gov/Safety/Recalls/ucm247658.htm
In Hong Kong, the above products manufactured by H&P Industries, Inc. are not registered pharmaceutical products.
Ends/ Monday, March 21, 2011
Issued at HKT 12:30
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