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Johnson & Johnson has recalled its laparoscopic power morcellators. These devices are used in hysterectomy procedures and other uterine surgical procedures. The Food and Drug Administration has discovered that the morcellators can spread malignant cancer cells. The device has been used by women to avoid invasive surgeries for removing fibroids from the uterus. Women who […]

At Terrell Hogan, we think recall information is worth repeating to keep your family informed and safe. Defective and dangerous products can cause personal injuries and deaths and need to be taken out of use or repaired. In December, 2013 we notified consumers about the dangers from old and new tires. Dangers from New Tires […]

Playtex is recalling AC/DC power adapters that are used with the Playtex Nurser Deluxe Double Electric Breast Pump. The casing on some adapters may become loose and separate, resulting in the possibility of electric shock. Women should immediately discontinue use if the adapter shows signs of separating. No injuries have been reported yet, but there […]

The OmniPod Insulin Management System has a built-in FreeStyle Blood Glucose Meter and the FreeStyle® blood glucose test strips may produce erroneously low blood glucose results. This is critical to Diabetics who as a result of inaccurate information may end up with high blood sugar and potentially coma. Symptoms of hyperglycemia, high blood sugar, may […]

The FDA has issued a Safety Communication headlined: “HeartStart Automated External Defibrillators (AED) From Philips Healthcare: Safety Communication – Failure Of An Electrical Component That Could Cause AEDs To Fail To Deliver Appropriate Shock.” There is a recall of 700,000 Philips Healthcare Automated External Defibrillators (AEDs) because there is a possibility of failure in life […]

A voluntary recall of certain lots of Nova Max Glucose Test Strips has occurred.  It has been determined that these strips may cause a false, abnormally high blood sugar level to be reported. A falsely high blood sugar level could result in an insulin dosing error (taking too much insulin) that could lead to a […]

Abbott Diabetes Care, the maker of the Freestyle Insulinx blood glucose meter, has initiated a voluntary Class I recall of this meter. A Class I is the most serious type of recall, involving a reasonable probability that use of this product will cause serious adverse health consequences. These meters display and store in memory an […]

At extremely high blood glucose levelsthe OneTouch Verio IQ Meter will turn off instead of displaying the message “EXTREME HIGH GLUCOSE above as intended.  Close to 2 million OneTouch Verio blood glucose meters are being recalled. FDA Warning

Pfizer has voluntarily recalled 14 lots of Lo/Ovral-28 tablets and 14 groups of the generic versions of the pill — one million total pill packs were recalled due to a packaging error. Many women have already been effected by birth control pill recalls in Jacksonville, FL. If you or someone you know has been effected, […]

The U.S. Food and Drug Administration has issued a recall warning for specific lots of Kotex tampons contaminated with a bacterium that could cause vaginal infections and other health risks. The recall is limited to two specific lots of Kotex Natural Balance Security Unscented Tampons Regular Absorbency manufactured by Kimberly-Clark. According to the FDA, both […]

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