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SafetyAlerts
November 6, 2002

International Specialty Products Has Recalled Plasdone K-29/32

(SafetyAlerts) - The Food and Drug Administration (FDA) released the following information.

PRODUCT
Plasdone K-29/32 (Povidone, USP/Ph.Eur. K-30), 110 lb drums. Recall # D-
045-3.

CODE
Lot 0500035188 and 0500035268.

RECALLING FIRM/MANUFACTURER
Recalling Firm: International Specialty Products, Wayne, NJ, by letters
dated November 27, 2000.
Manufacturer: ISP Technologies, Texas City, TX.
Firm initiated recall is ongoing.

REASON
Product contains metal particles

VOLUME OF PRODUCT IN COMMERCE
Lot 05000035188: 24,200 lbs; Lot 05000035268, 13,310 lbs.

DISTRIBUTION
OH, DE, IL,
MI, PA, VA, NY, ME and Internationally.

 
Selected Recent Recalls


Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.