Posts Tagged ‘patient safety’

Recalls and Safety Alerts: Recall of Procrit and Epogen

Amgen is recalling certain lots of Procrit (epoetin alfa) and Epogen (epoetin alfa) because the vials may contain very thin flakes of glass. These glass flakes, which are barely visible, appear to come from the inner surface of the glass vials and ar…

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Recalls and Safety Alerts: Expanded Recall of Multi-Med Huber Needles/Sets

The medical products company Multi-Med is expanding an earlier recall of the company’s Huber needles. These products are being recalled because of the potential for the needles to core.

Huber needles are used to access implanted ports in patients…

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Recalls and Safety Alerts: BagEasy Resuscitation Devices Recalled

WestMed, Inc., is recalling certain lots of BagEasy manual resuscitation devices, because a disconnection could occur at the retention ring of the patient port manifold. This could cause the unit not to work, delaying resuscitation while the user fi…

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Recalls and Safety Alerts: More Patient Burns from Dental Handpieces

FDA is again alerting dental professionals about the possibility of serious patient burns from electric dental handpieces that overheat. Some patients have experienced third-degree burns that required reconstructive surgery. Although FDA issued a w…

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Preventing Medical Errors: Preventing Fires in the Operating Room

An estimated 600 surgical fires occur each year in the U.S. Although most are minor, some result in serious injury, disfigurement, or even death.
The Anesthesia Patient Safety Foundation (APSF) says the vast majority of these fires are preventable….

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Preventing Medical Errors: Sterility Issues with AVM Clips

Microneurosurgical clips are used to occlude small vessels during surgery for intracranial arteriovenous malformations (AVM). Some AVM clips are supplied sterile and some are not, and this can cause confusion. For example, FDA received a report abo…

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FDA Consumer Corner: Don?t Use Infant Sleep Positioners

FDA and the Consumer Product Safety Commission (CPSC) are warning people not to use sleep positioners for their babies, because there is a chance they could suffocate. In the last 13 years, at least 12 babies between the ages of one and four months …

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Recalls and Safety Alerts: Aseptic Meningitis with Lamictal

FDA is informing healthcare professionals and patients that the drug Lamictal (lamotrigine) can cause aseptic meningitis. Lamictal is approved to treat bipolar disorder in adults, and seizures in adults and children two years and older.

FDA’s r…

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Recalls and Safety Alerts: Preventing Bloodborne Infections When Using Fingerstick Devices

FDA and CDC are alerting healthcare professionals and patients about the risk of transmitting hepatitis B virus (HBV) and other infectious diseases when fingerstick lancing devices are used on more than one person. These devices puncture the skin to…

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Recalls and Safety Alerts: Recall of INOMAX DS Drug Delivery System

The manufacturer Ikaria is recalling its INOMAX DS drug delivery system because a pressure switch in the device may fail. INOMAX delivers nitric oxide, a vasodilator, to treat term and near-term neonates with hypoxic respiratory failure associated w…

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