December, 2010American Honda Recalls Snowblowers Due to Fire Hazard

The fuel tank joint and o-ring located on the underside of the fuel tank can seep or drip fuel over time, posing a fire hazard.

Sodium Bicarbonate Injection, USP, 7.5% and 8.4%, 50 mL Single Dose Vials – Recall Due to Particulates in Some Vials

Audience: Hospital Risk Managers, Pharmacy, Emergency Medicine ISSUE: American Regent and FDA notified healthcare professionals of the nationwide recall of  specific lots of Sodium Bicarbonate Injection, USP, 7.5% and 8.4%, 50 mL Single Dose Vials…

Dexamethasone Sodium Phosphate Injection, 4 mg/mL, 30 mL Multiple Dose Vial: Recall due to Particulates in Product

Audience: Risk Managers, Pharmacists Issue: American Regent and FDA notified healthcare professionals of the nationwide recall of specific lots of Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL, 30 mL Multiple Dose Vial because some vials of…

BabyLegs Recalls Baby Socks and Leg Warmers with Heart Applique Due to Choking Hazard

The leg warmers and socks have a heart applique that can detach, posing a choking hazard to small children.

LexisNexis® Legal News Podcast for December 23, 2010

On this edition, a summary of the some of the legal news stories reported by the editors LexisNexis Mealeys during the fourth quarter of 2010. Hear these and other stories from LexisNexis® Mealey’s™ Publications. Copyright© 2010 LexisNexis, a divis…

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LexisNexis® Legal News Podcast for December 23, 2010

On this edition, a summary of the some of the legal news stories reported by the editors LexisNexis Mealeys during the fourth quarter of 2010. Hear these and other stories from LexisNexis® Mealey’s™ Publications. Copyright© 2010 LexisNexis, a division of Reed Elsevier Inc. For the latest litigation news headlines, visit www.lexisnexis.com/mealeys or www.lexisnexis.com/community.

RockHard Weekend, Pandora: Recall – Undeclared Drug Ingredient

Audience: Consumer ISSUE: FDA notified the public that testing determined that certain lots of these products contain an analogue of sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED). The active drug ingredient…

Lipitor (atorvastatin) 40 mg: Recall Specific Bottles

Audience: Family Practice, Patient, Pharmacy UPDATED 12/23/2010: Pfizer announced a recall of one lot — 19,000 bottles — of Lipitor 40 mg tablets (atorvastatin calcium) distributed in the U.S. There were three earlier recalls of Lipitor,…

Fruta Planta: Public Notification – Undeclared Drug Ingredient

Audience: Consumer, Family Practice, Cardiology ISSUE: FDA has received multiple reports of adverse events associated with the use of Fruta Planta, including several cardiac events and one death. FDA laboratory analysis confirmed that Fruta Planta…

LexisNexis® Legal News Podcast for December 22, 2010

On this edition, a summary of the some of the legal news stories reported by the editors LexisNexis Mealeys during the third quarter of 2010. Hear these and other stories from LexisNexis® Mealey’s™ Publications. Copyright© 2010 LexisNexis, a divisi…

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