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Abbott Laboratories Has Recalled Erythromycin

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

PRODUCT
Erythromycin, USP Base, Dihydrate, Code No. 79147, bulk drug (drum), Caution: For Manufacturing, Processing or Repacking, Rx Only. Recall # D-250-3.

CODE
Lot 72332CD00, Exp.12/13/05.

RECALLING FIRM/MANUFACTURER
Abbott Laboratories, North Chicago, IL, by letter on April 25, 2003. Firm initiated recall is ongoing.

REASON
Failure of x-ray identification limit for monohydrate form.

VOLUME OF PRODUCT IN COMMERCE
Portion of one lot to a single manufacturer

DISTRIBUTION
NY.