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FDA Recalls

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466 American Regent Initiates Nationwide Voluntary Recall of Epinephrine Injection, USP, 1:1000, 1mL Ampules Lot #1395 Due to Discoloration and Small Visible Particles Wednesday, 25 April 2012
467 XROCK INDUSTRIES, LLC Issues a Voluntary Nationwide Recall of X-ROCK, a Product Marketed as a Dietary Supplement To Support Male Sexual Performance, Due to Unlisted, Potentially Hazardous Ingredient Saturday, 21 April 2012
468 Hong Lee Trading Inc. Issues An Alert On Undeclared Sulfites In Peacock Brand Preserved Apricots Wednesday, 18 April 2012
469 M.E. Thompson, Inc. Expands Recall of Sub Sandwiches Because of Possible Health Risk Wednesday, 18 April 2012
470 Hospira Announces a Nationwide Voluntary Recall of One Lot of Morphine Sulfate Injection, USP 4 MG/ML, (C-II) 1 ML Fill in 2.5 ML Carpuject, That May Contain More Than The Intended Fill Volume Tuesday, 17 April 2012

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