Teleflex Recalls Iso-Gard Filter S for Risk of Splitting or Detaching That May Cause Leakage and Insufficient Air Supply to Patients Test words
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The Danger of Infant Head Shaping Pillows
Do Not Use Infant Head Shaping Pillows to Prevent or Treat Any Medical Condition- FDA Safety Communication Today, the U.S. Food and Drug Administration (FDA) is warning parents, caregivers, and health care providers not to use infant head shaping pillows intended to change an infant’s head shape and/or symmetry or claim to prevent or treat any medical condition. …
Do Not Use Ultraviolet (UV) Wands That Give Off Unsafe Levels of Radiation
The U.S. Food and Drug Administration (FDA) continues to warn consumers about the potential risk of injury associated with the use of certain brands of ultraviolet (UV) wands. Do not use these UV wands because they may expose you or any nearby person to unsafe levels of ultraviolet-C (UV-C) radiation and may cause injury to the skin, eyes, or both …
CereLink ICP Monitor by Integra: Class I Recall – Due to Risk of Incorrect Intracranial Pressure Readings
Integra is recalling the CereLink ICP Monitor, Model #826820/826820P, after reports that the device may display incorrect values for a patient’s intracranial pressure and display out-of-range pressure readings. If the device is not working properly, the patient may have to undergo additional brain surgeries to replace it, which involves the risks of infection, bleeding, and damage to tissue. Additionally, because …
Medtronic Recalls HeartWare HVAD System Batteries for Electrical Faults That Cause Battery Failure
Medtronic, Inc. is recalling HeartWare HVAD System batteries because the batteries may experience electrical faults that cause them to unexpectedly fail. When this occurs, batteries with an electrical fault may be unable to power the controller, unable to accept charge from the battery charger, or appear to remain charged when in use. The U.S. Food and Drug Administration (FDA) has …
SIGMA Spectrum Infusion Pump Recall
On December 29, 2021, Baxter Healthcare issued an Urgent Safety Communication regarding the SIGMA Spectrum Infusion Pumps with Master Drug Library (Version 8) and Spectrum IQ Infusion Systems with Dose IQ Safety Software (Version 9) due to the risk of not alarming for repeated upstream occlusion events. After an upstream occlusion alarm, failure to fully resolve any upstream occlusion before …
Button Battery from Target Mini X-Mas Tree Injures Toddler
A toddler in Lincoln, Nebraska was seriously injured from a button battery that came from a mini Christmas tree decoration that his mother purchased at Target. The Meyerson Law Firm investigation has determined the lighting tester button contains a button battery that can be easily accessed by tugging on the wire. This makes the device non-compliant with UL safety standard …
Button Battery From Midea Remote Injures Child
The Meyerson Law Firm is representing the mother of a child in New York City who was injured swallowing a button battery that came from a Midea Air Conditioner remote control. The housing for the battery in the remote at issue opens without the need of a coin or tool. The Consumer Products Safety Commission has been notified.
Medical Malpractice
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Construction Accidents
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