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5 Percent Dextrose Injection USP in PAB Container by B. Braun Medical: Recall
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OxySure Portable Emergency Oxygen System, Model 615 by OxySure Therapeutics, Inc: FDA Safety Communication
[Posted 03/29/2016] AUDIENCE: Consumer, Health Care Providers ISSUE: The FDA is recommending consumers, businesses, schools, and health care providers stop using OxySure Portable Emergency Oxygen System, Model 615 because of several device malfunctions, including ineffective oxygen delivery, and chemical reactions in the canisters that could cause them to explode. Due to adverse event reports to…
Compounded Products by Reliable Drug Pharmacy: Recall
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Best Bentonite Clay by Best Bentonite: FDA Alert
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NOW Health Group Dietary Supplements: Recall
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Opioid Pain Medicines: Drug Safety Communication
[Posted 03/22/2016] AUDIENCE: Family Practice, Psychiatry, Pain Management, Nursing, Endocrinology ISSUE: FDA is warning about several safety issues with the entire class of opioid pain medicines. See the FDA Drug Safety Communication for a complete listing. These safety risks are potentially harmful interactions with numerous other medications, problems with the adrenal glands, and decreased sex hormone levels….
Sodium Bicarbonate Injection, USP by Hospira: Recall
[Posted 03/21/2016] AUDIENCE: Pharmacy, Nursing ISSUE: Hospira, Inc. is recalling one lot of 8.4% Sodium Bicarbonate Injection, USP (NDC: 0409-6625-02, Lot 56-148-EV, Expiry 1AUG2017) at the hospital/retail level due to the presence of a particulate within a single–dose glass fliptop vial. The issue was identified through a confirmed complaint. The product is packaged 50 mEq…
GlideScope Titanium Single-Use Video Laryngoscope by Verathon: Class I Recall
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Eye Drops: FDA Statement
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