-
Recent Posts
Categories
- Anesthesiology
- Avandia
- Cardiology
- Clinics
- Consumer Products
- Emergency Rooms
- Endocrinology
- Eye Care
- Family Practice
- FDA 2011
- FDA 2012
- FDA Label Change
- FDA Notice
- FDA Recall
- FDA Safety Communication
- FDA Warning
- Gastroenterology
- Healthcare Professionals
- Hematology
- Hospitals
- Infectious Disease
- Internal Medicine
- Laboratory
- multiple sclerosis (MS)
- Neurology
- OBGYN
- Oncology
- Ophthalmology
- Pain Management
- Patients
- Pediatrics
- Pharmacy
- Psychiatry
- Radiology
- Rheumatology
- Risk Manager
- Uncategorized
Tag Archives: FDA recall
Automated External Defibrillators AEDs Class I Recall
Cardiac Science Powerheart, CardioVive, CardioLife; GE Responder and Responder Pro; and Nihon-Kohden Automated External Defibrillators (AEDs): Class I Recall – Defective Component Affected Models include: Powerheart 9300A, 9300E, 9300P, 9390A, and 9390E CardioVive 92532, 92533 CardioLife 9200G and 9231 GE … Continue reading
Posted in Cardiology, Emergency Rooms, FDA 2012, FDA Recall, Risk Manager
Tagged AEDs, Automated External Defibrillators, Cardiac Science Powerheart, CardioLife, Cardiology, CardioVive, Class 1 Recall, Class I Recall, Defective Component, Emergency Medicine, FDA recall, GE Responder, Nihon-Kohden, Recall, Responder Pro
Comments Off
Flight Medical V240040029 Cable for Newport HT50 Ventilator Class I Recall
Flight Medical V24-00400-29 Cable for Newport HT50 Ventilator: Class I Recall – Cable May Cause an Electrical Shortage That can Cause Ventilators to Shutdown Unexpectedly ISSUE: The recalled cable may cause an electrical shortage that can cause Newport HT50 … Continue reading
Norgestimate and Ethinyl Estradiol Tablets Recall
Norgestimate and Ethinyl Estradiol Tablets: Recall – Packaging Error, Potential for Incorrect Dosing Regimen AUDIENCE: OB/GYN, Pharmacy, Patient ISSUE: Glenmark Generics Inc. issued a nationwide, consumer-level recall of seven (7) lots of Norgestimate and Ethinyl Estradiol Tablets USP (0.18 mg/0.035 … Continue reading
Posted in OBGYN, Pharmacy
Tagged Birth Control Pills, Dietary Supplements, drug risks, Ethinyl Estradiol Tablets, Family Practice, FDA recall, Norgestimate, Norgestimate and Ethinyl Estradiol Tablets Recall, OBGYN, Oral Contraceptives, Packaging Error, Patient, Pharmacy, Recall
Comments Off
Cytarabine for Injection 1 gm vial Bedford Labs Recall
Cytarabine for Injection, 1 gm/vial [Bedford Labs]: Recall: Risk of Lack of Sterility ISSUE: Bedford Laboratories announced a nationwide recall of three lots of cytarabine for injection—2066986, 2111675, and 2131148—because vials have a potential risk of a lack of sterility. The risk … Continue reading
Posted in Clinics, Emergency Rooms, Family Practice, FDA 2012, FDA Recall
Tagged 1 gm vial, Bedford Labs, Clinics, Cytarabine for Injection, Cytarabine for Injection 1 gm vial Bedford Labs Recall, drug risks, Emergency Rooms, Family Practice, FDA recall, Hospitals, Pharmacy, physician offices, Recall
Comments Off
Phenylephrine HCl Injection USP 1% 5 mL Vial Recall
UPDATED 02/23/2012] Phenylephrine HCl Injection, USP, 1% 5 mL Vial, (Lot# 0693) recalled. AUDIENCE: Pharmacy ISSUE: Recall initiated because some vials exhibit translucent visible particles consistent with glass delamination. Potential adverse events after intravenous administration include damage to blood vessels … Continue reading
Posted in Clinics, Emergency Rooms, FDA 2012, Hospitals, Pharmacy
Tagged (Lot# 0693), 1% 5 mL Vial, American Regent, Clinics, drug risks, Emergency Rooms, fda, FDA recall, Home Health Care Agencies, Hospitals, Infusion Centers, Pharmacy, Phenylephrine HCl Injection, Recall, USP)
Comments Off
Infants TYLENOL Oral Suspension 1 oz Grape Recall
Infants’ TYLENOL Oral Suspension, 1 oz. Grape: Recall – Dosing System Complaints AUDIENCE: Consumer, Pharmacy ISSUE: McNeil Consumer Healthcare notified the public of a recall of seven lots (approximately 574,000 bottles) of Infants’ TYLENOL Oral Suspension, 1 oz. Grape. There … Continue reading
Posted in Consumer Products, FDA 2012, FDA Recall, Pharmacy
Tagged 1 oz Grape, Consumer, Dosing System Complaints, drug risks, FDA recall, Infants TYLENOL, Infants TYLENOL Oral Suspension 1 oz Grape Recall, McNeil Consumer Healthcare, Oral Suspension, Pharmacy, Recall, SimpleMeasure dosing system
Comments Off
Wholistic Herbs Inc Koff and Kold Kold Sore Spray Recall
Wholistic Herbs, Inc. “Koff and Kold” and “Kold Sore” Spray: Recall – Non-Sterile Products AUDIENCE: Consumer ISSUE: Wholistic Herbs Inc. notified the public it is recalling all quantities of “Koff & Kold” spray with herbal extract and “Kold Sore” spray … Continue reading
Posted in Consumer Products, FDA 2012, FDA Recall
Tagged cold remedy, Dietary Supplements, drug, drug risks, FDA recall, Koff and Kold, Kold Sore Spray, Over the counter, Recall, Wholistic Herbs Inc, Wholistic Herbs Inc Koff and Kold Kold Sore Spray Recall
Comments Off