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11.07	N.C. Firm Recalls Heparin Flush Syringes BETHESDA, MD, 21 December 2007 — AM2PAT Inc. in North Carolina is recalling lot 070926H of the firm's heparin-containing flush-solution product because of contamination with Serratia marcescens, according to a press release dated December 20 and circulated today by FDA.
10.07	Defer Hib Vaccine Booster in Most Children, CDC Says BETHESDA, MD, 19 December 2007 — Issues related to a recall of Merck & Co.'s Haemophilus influenzae type b (Hib) conjugate vaccines will cause them to be in short supply, prompting federal officials today to recommend temporary changes to the childhood immunization schedule.
10.07	New Beta-Blocker Gets FDA Approval "BETHESDA, MD, 18 December 2007 — A new beta-blocker from Mylan and Forest Laboratories was approved Monday for marketing in the United States, FDA announced.

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