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Consumers are advised by the FDA not to use Bullet Proof because it contains undeclared tadalafil which, when interacting with nitrates, may lower blood pressure to dangerous levels. Background of Bullet Proof Bullet Proof is promoted for sexual enhancement. FDA Alert on Bullet Proof Laboratory analysis by the FDA confirmed that Bullet Proof contains tadalafil, [...]

The FDA informs consumers that Lightning Rod capsules are recalled because it contains an analogue of Sildenafil, active ingredient of an FDA-approved drug, making Lightning Rod an unapproved new drug. Background of Lightning Rod Capsules Lightning Rod, by Chang Kwung, is marketed as a dietary supplement for male sexual enhancement. It is sold in capsules [...]

Anesthesiology, biomedical engineering, nursing personnel and risk managers are informed by the FDA that Maquet Servo-I Ventilator Battery Module is recalled because the battery has a shorter runtime than expected and may cause serious adverse events and/or death. Background of Maquet Servo-I Ventilator Battery Module The Servo-I system, by Maquet, is used for the treatment [...]

The FDA warns neurology, nursing, risk managers and surgery personnel that Medtronic Deep Brain Stimulation Lead Kit and Activa Dystonia HDE Kit are recalled due to potential for damage that may cause lead replacement. Background of Deep Brain Stimulation Lead Kit & Activa Dystonia HDE Kit Deep Brain Stimulation systems provide electrical stimulation to selected [...]