Natural Wellness is warning consumers not to purchase or consume the product known as MasXtreme, Lot# 911035. This product which is being marketed as a dietary supplement contains undeclared amounts of Aildenafil, as well as the drug Phentolamine which is an alpha-adrenergic blocker. Aildenafil is close in structure to Sildenafil and is expected to … [Read more...]
The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex That May Contain Particulate Matter
Teleflex Incorporated Announces Worldwide Voluntary Recall of Arrow Select IV Tubing Sets, Accessories, and Certain Embolectomy Catheters
LifeScan Recalls 8 Lots of OneTouch, SureStep Test Strips Due To Inaccurate
LifeScan, Inc. is recalling eight lots of OneTouch ® SureStep ® Test Strips, used by people with diabetes to measure their blood glucose levels at home. The test strips are being recalled because they may provide falsely low glucose results when the glucose level is higher than 400 mg/dL. The eight lots of consumer OneTouch SureStep Test Strips … [Read more...]
Acacia Recalls IV Extension Sets with BD Q-Syte Luer Access Device
Acacia, Inc. (formally known as MPS Acacia) has voluntarily executed a product recall of certain lots of IV Extension Sets with BD Q-Syte™ Luer Access Device. The BD Q-Syte™ Luer Access Device is a Needleless Valve manufactured by BD (Becton, Dickinson and Company). Use of the affected BD Q-Syte™ Luer Access Device may cause an air embolism or … [Read more...]
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