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Alertes médicamenteuses de la FDA
ALERTES AUX DROGUES DE LA FDA
APR
07
Nalpac Issues Voluntary Nationwide Recall of DTF Sexual Chocolate Due to the Presence of the Pharmaceutical Ingredients Sildenafil and Tadalafil
By:
on
APR
07
Audience: Consumer April 07, 2026 Ferndale, Michigan. Nalpac is voluntarily recalling DTF Sexual Chocolate it purchased and resold. The products have been found to contain sildenafil and tadalafil. Nalpac is not the manufacturer of this...
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MAR
31
FDA Identifies Cases of Serious Liver Injury in Patients Taking Tavneos (avacopan) for Severe Active Anti-Neutrophil Cytoplasmic Autoantibody Associated Vasculitis
By:
on
MAR
31
Audience: Health Care Professional March 31, 2026 - FDA Identifies Cases of Serious Liver Injury in Patients Taking Tavneos (avacopan) for Severe Active Anti-neutrophil Cytoplasmic Autoantibody (ANCA)-associated Vasculitis What Is FDA Doing? FDA...
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MAR
30
Aphreseller Issues Voluntary Recall of Kian Pee Wan Capsules Due the Presence of Undeclared Dexamethasone and Cyproheptadine
By:
on
MAR
30
Audience: Consumer March 30, 2026 - Flushing, New York, Aphreseller (Ebay seller ID), Buy-herbal.com is recalling all lots of Kian Pee Wan capsules to the consumer level. FDA analysis has found that the product contains the undeclared drug...
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MAR
24
Amneal Issues Recall of Magnesium Sulfate in Water for Injection, USP 4 g/100mL (NDC 70121-1720-3) Due to Product Mix-Up
By:
on
MAR
24
Audience: Health Care Professional, Pharmacy March 24, 2026 – Bridgewater, New Jersey, Amneal Pharmaceuticals LLC is voluntarily recalling one lot of Magnesium Sulfate in Water for Injection, USP, 4g/100mL, IV bag, to the hospital level. A...
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MAR
20
FDA Is Requiring Warning about Vitamin B6 Deficiency and Associated Seizures for Drug Products Containing Carbidopa/Levodopa
By:
on
MAR
20
Audience: Health Care Professionals March 20, 2026 -- FDA Is Requiring Warning about Vitamin B6 Deficiency and Associated Seizures for Drug Products Containing Carbidopa/Levodopa What Is FDA Doing? The U.S. Food and Drug Administration (FDA) has...
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MAR
19
Cardinal Health Issues Voluntary Nationwide Recall of Webcol™ Large Alcohol Prep Pad
By:
on
MAR
19
Audience: Consumer, Health Care Professionals DUBLIN, Ohio, March 19, 2026 – Cardinal Health has issued a voluntary recall for select lots of Webcol™ Large Alcohol Prep Pads (70% isopropyl alcohol) to the consumer level. The product is...
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MAR
14
Pure Vitamins and Natural Supplements, LLC Issues Voluntary Nationwide Recall of Honey Products Due to Undeclared Sildenafil and Tadalafil
By:
on
MAR
14
Audience: Consumer March 14, 2026- Pure Vitamins and Natural Supplements, LLC of Tampa, FL is voluntarily recalling Boner Bear Honey, Red Bull Extreme and Blue Bull Extreme. FDA laboratory analysis confirmed that Boner Bear Honey, contains...
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MAR
11
Primal Herbs Issues Voluntary Nationwide Recall of Primal Herbs Volume Due to Undeclared Sildenafil
By:
on
MAR
11
Audience: Consumer FDA Publish Date: March 11, 2026 -- FOR IMMEDIATE RELEASE - February 27 2026 — Albuquerque, New Mexico, Primal Supplements Group LLC is voluntarily recalling all orders of Primal Herbs Volume placed between July 2 and...
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MAR
06
Integra LifeSciences Removes Certain MediHoney and CVS Wound and Burn Products
By:
on
MAR
06
Audience: Consumer March 6, 2026The FDA has since determined that this device may cause temporary or reversible health problems, or—though unlikely—serious health problems. The affected products and recommendations for what to do with...
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FEB
27
USA LESS Co. is Recalling Rhino Choco VIP 10X Due to Undeclared Tadalafil
By:
on
FEB
27
Audience: Consumers BROOKLYN, N.Y., Feb. 27, 2026 /PRNewswire/ -- USALESS.COM is recalling its RHINO CHOCO VIP 10X, in 10 gr, 12 pc packages that come in a black cardboard box marked with UPC Code 724087947668 on the back and with an expiration date...
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