Skip Navigation Skip to Sitemap

Patient Safety Program Banner

Alerts

***ISMP issues a NEW NAN ALERT***

FDA MedWatch Safety Alerts Archive

 MMQC Alerts

MMQC-12-1306
Endo Pharmaceuticals Inc. / Endocet (Oxycodone/Acetaminophen, Usp) / Urgent Drug Recall / DLA 12-160 / Recall To Retail Level


Manufacturer has issued a recall on the FOL MATL on 07 MAY 2012. Reason: One bottle from lot was found to contain some Endocet 10/325mg tablets. DISP: Comply with manufacturer distribution instructions if received. Examine stock immediately. Stop dispensing, distributing and quarantine inventory.

MMQC-12-1240
Immediate Message/Ben Vue Laboratories Inc./Polymyxin B for Injection Sterile/Vecuronium Bromide for Injection/FDA Class 1 Recall/DLA 12-130


FDA Class 1 Recall on FOL MATL. Reason: Presence of particulate matter: The potential for glass particulates in these lots of product cannot be eliminated.



MMQC-12-1239
Immediate Message/Glenmark Generics Inc./Norgestimate and Ethinyl Estradiol Tablets USP/FDA Class 1 Recall/DLA 12-061A


FDA Class 1 Recall on FOL MATL. Reason: Implemented because of a packaging error, where select blisters were rotated 180 degrees within the card, reversing the weekly tablet orientation and making the lot number and expiry date visible only on the outer pouch.



MMQC-12-1209
Immediate Message/Boehringer Ingelheim, Roxane Laboratories/Ben Venue Laboratories (BVL)/Acetylcysteine Solution/FDA Class 1 Recall/DLA 11-460


SUSPENSE: 4/11/2012
FDA Class 1 Recall on FOL MATL. Reason: Due to the presence of a single glass particle. DISP: Comply with manufacturer distribution instructions if received. Contact any patients that may have received dispensed product and request patients affected lot.



MMQC Alerts Archive