|
MMQC-07-1142 |
FDA ADVISES MANUFACTURERS TO
TEST GLYCERIN FOR POSSIBLE CONTAMINATION / FDA
MEDWATCH |
|
MMQC-07-1141 |
PARKEDALE PHARMACEUTICALS /
BREVITAL C-IV (METHOHEXITAL SODIUM FOR
INJECTION) / URGENT DRUG RECALL / DSCP 07-084 |
|
MMQC-07-1139 |
ABBOTT LABORATORIES / VARIOUS
ARCHITECT ESTRADIOL REAGENT TEST KITS / PRODUCT
CORRECTION / DSCP 07-067 |
|
MMQC-07-1138 |
ABBOTT LABORATORIES / VARIOUS
ARCHITECT STAT TROPONIN-I REAGENT TEST KITS /
PRODUCT CORRECTION / DSCP 07-079 |
|
MMQC-07-1135 |
FDA PROPOSES NEW WARNINGS ABOUT
SUICIDAL THINKING, BEHAVIOR IN YOUNG ADULTS WHO
TAKE ANTIDEPRESSANT MEDICATIONS / MEDWATCH |
|
MMQC-07-1134 |
2007 SAFETY ALERT: COLCHICINE
COMPOUNDED INJECTABLE PRODUCTS / MEDWATCH |
| April
2007 |
|
|
MMQC-07-1130 |
ANTHRAX VACCINE EXPIRATION
90-DAY NOTICE LOT FAV103 |
|
MMQC-07-1127 |
BIOMET INC / VARIOUS KITS /
URGENT PRODUCT RECALL / DSCP 07-053 |
|
MMQC-07-1126 |
BOSTON SCIENTIFIC / VAXCEL
IMPLANTABLE CHEST PORTS WITH PASV VALVE
TECHNOLOGY / URGENT MEDICAL DEVICE RECALL / DSCP
07-048 |
|
MMQC-07-1125 |
MAJOR MANUFACTURER OF UNAPPROVED
AND ADULTERATED DRUGS AGREES TO STOP ILLEGAL
PRACTICES / FDA MEDWATCH |
|
MMQC-07-1124 |
GENENTECH / AVASTIN (BEVACIZUMAB)
/ IMPORTANT DRUG WARNING / FDA MEDWATCH SAFETY
INFORMATION |
|
MMQC-07-1122 |
QUADRIVALENT HUMAN
PAPILLOMAVIRUS VACCINE: RECOMMENDATIONS OF THE
ADVISORY COMMITTEE ON IMMUNIZATION PRACTICES |
|
MMQC-07-1117 |
FDA SEIZES ALL MEDICAL PRODUCTS
FROM N.J. DEVICE MANUFACTURER FOR SIGNIFICANT
MANUFACTURING VIOLATIONS / FDA NEWS |
|
MMQC-07-1116 |
ORTHO-MCNEIL PHARMACEUTICALS /
GRISEOFULVIN ORAL SUSPENSION / VOLUNTARY RECALL
/ DSCP 07-075 |
|
MMQC-07-1115 |
GLAXOSMITHKLINE / THIRD-PARTY
TAMPERING (COUNTERFEIT) OF ZIAGEN (ABACAVIR
SULFATE) TABLETS AS COMBIVIR(LAMIVUDINE AND
ZIDOVUDINE) TABLETS / MEDWATCH |
|
MMQC-07-1110 |
ACORDA THERAPEUTICS / CHANGES TO
THE CONTRAINDICATIONS AND WARNING SECTIONS OF
ZANAFLEX (TIZANIDINE HYDROCHLORIDE) / FDA
MEDWATCH |
|
MMQC-07-1109 |
UNAPPROVED SUPPOSITORY DRUG
PRODUCTS CONTAINING TRIMETHOBENZAMIDE
HYDROCHLORIDE / FDA MEDWATCH SAFETY INFORMATION |
|
MMQC-07-1105 |
PERMAX (PERGOLIDE) AND GENERIC
EQUIVALENTS / FDA MEDWATCH NOTICE DRUG
WITHDRAWAL |
|
MMQC-07-1104 |
WARNING ABOUT BUYING ACCUTANE (ISOTRETINOIN)
ONLINE / FDA MEDWATCH |
|
MMQC-07-1103 |
NOVARTIS / ZELNORM (TEGASEROD
MALEATE) / FDA MEDWATCH SAFETY NOTICE |
| March
2007 |
|
|
MMQC-07-1099 |
SANOFI-AVENTIS / KETEK (TELITHROMYCIN)
/ LABEL CHANGE / FDA MEDWATCH |
|
MMQC-07-1091 |
ANTHRAX VACCINE EXPIRATION
90-DAY NOTICE LOT FAV102 |
|
MMQC-07-1090 |
COSMOS TRADING INC. ISSUES
VOLUNTARY NATIONWIDE RECALL OF RHINO MAX (RHINO
V MAX), A PRODUCT MARKETED AS A DIETARY
SUPPLEMENT / FDA MEDWATCH |
|
MMQC-07-1089 |
SAFETY CONCERNS / ZYVOX (LINEZOLID)
/ FDA MEDWATCH |
|
MMQC-07-1088 |
IMMEDIATE MESSAGE / HOMEDICS /
HEATING PADS / UPGRADED FDA CLASS I / DSCP
07-035 |
|
MMQC-07-1087 |
MERCK & CO INC / PNEUMOVAX 23 /
VOLUNTARY RECALL / DSCP 07-059 |
|
MMQC-07-1086 |
MERCK & CO INC / VARIOUS
VACCINES (RECOMBIVAX HB, COMVAX, VAQTA, &
PEDVAXHIB) / VOLUNTARY RECALL / DSCP 07-052 |
|
MMQC-07-1084 |
REQUEST FOR LABELING CHANGE FOR
SEDATIVE-HYPNOTIC DRUGS / FDA MEDWATCH |
|
MMQC-07-1082 |
TAKEDA / ACTOS (PIOGLITAZONE)
TABLETS / FDA MEDWATCH SAFETY NOTICE |
|
MMQC-07-1081 |
FDA STRENGTHENS SAFETY
INFORMATION FOR ERYTHROPOIESIS-STIMULATING
AGENTS (ESAS) / FDA MEDWATCH |
|
MMQC-07-1080 |
TERMINATION OF THE INSPIRE
CLINICAL STUDY OF ACTIMMUNE / FDA MEDWATCH
HEALTH ADVISORY |
|
MMQC-07-1077 |
GEBAUER / SALIVART ORAL
MOISTURIZER / PRODUCT RECALL / DSCP 07-046 |
|
MMQC-07-1074 |
REMEL / MACCONKEY AGAR WITH
SORBITOL / IMPORTANT MEDICAL DEVICE CUSTOMER
ADVISORY NOTICE / DSCP 07-044 |
|
MMQC-07-1073 |
UPDATED ANTHRAX AND SMALLPOX
VACCINE MONTHLY INVENTORY |
|
MMQC-07-1071 |
BAXTER / VENTED PACLITAXEL
ADMINISTRATION SETS / URGENT PRODUCT RECALL /
DSCP 07-043 |
|
MMQC-07-1070 |
WARNING OF POSSIBLE ADVERSE
EVENTS BECAUSE OF NEW DAYLIGHT SAVINGS TIME /
FDA MEDWATCH |
|
MMQC-07-1067 |
UNAPPROVED DRUGS CONTAINING
ERGOTAMINE TARTRATE FOR TREATMENT OF VASCULAR
HEADACHES / FDA MEDWATCH SAFETY INFORMATION |
|
MMQC-07-1064 |
EKOS / ENDOWAVE AND LYSUS
INFUSION SYSTEMS - DRUG DELIVERY CATHETERS /
URGENT DEVICE RECALL / DSCP 07-039 |
|
February 2007 |
|
|
MMQC-07-1058 |
OHM LABS / LORATADINE SYRUP /
URGENT DRUG RECALL / DSCP 07-010 |
|
MMQC-07-1052 |
BRISTOL-MYERS SQUIBB / BARACLUDE
(ENTECAVIR) TABLETS AND ORAL SOLUTION / FDA
MEDWATCH NOTICE |
|
MMQC-07-1051 |
ROCHE / STUDY TERMINATED / FDA
MEDWATCH SAFETY INFORMATION |
|
MMQC-07-1050 |
PATIENT MEDICATION GUIDES FOR
ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD)
/ FDA MEDWATCH SAFETY INFORMATION |
|
MMQC-07-1049 |
ALBUTEROL INHALATION AEROSOL /
AVAILABILITY OF PRODUCT |
|
MMQC-07-1048 |
GENENTECH / XOLAIR (OMALIZUMAB)
/ FDA MEDWATCH SAFETY NOTICE |
|
MMQC-07-1047 |
GLAXOSMITHKLINE (GSK) / AVANDIA
(ROSIGLITAZONE MALEATE) / FDA MEDWATCH SAFETY
INFORMATION
 |
|
MMQC-07-1046 |
ARANESP (DARBEPOETIN ALFA),
EPOGEN (EPOETIN ALFA), PROCRIT (EPOETIN ALFA) /
INFORMATION FOR HEALTHCARE PROFESSIONALS / FDA
MEDWATCH |
|
MMQC-07-1045 |
MERCK AND CO. INC / ROTATEQ
(ROTAVIRUS VACCINE) / FDA MEDWATCH PUBLIC HEALTH
NOTIFICATION |
|
MMQC-07-1044 |
BECTON DICKINSON / INTEGRA 1ML
INSULIN SYRINGE / URGENT PRODUCT RECALL / DSCP
07-031
 |
|
MMQC-07-1039 |
SANOFI-AVENTIS / LABEL AND
INDICATION CHANGES FOR KETEK (TELITHROMYCIN) /
FDA MEDWATCH |
|
MMQC-07-1038 |
BAXTER / MEDICATION ERROR
INVOLVING TWO HEPARIN PRODUCTS / FDA MEDWATCH
 |
|
MMQC-07-1037 |
PUBLIC HEALTH ALERT TOPICAL
ANESTHETICS / FDA MEDWATCH |
|
MMQC-07-1031 |
PRECAUTIONS IN USING THE
REINTRODUCED VAPOTHERM / FDA MEDWATCH SAFETY
INFORMATION |
|
MMQC-07-1029 |
GENENTECH / LUCENTIS (RANIBIZUMAB
INJECTION) / FDA MEDWATCH SAFETY INFORMATION
|
|
MMQC-07-1028 |
COUNTERFEIT LIVIRO3 DISCOVERED
AFTER VOLUNTARY RECALL ANNOUNCEMENT / MEDWATCH
 |
|
MMQC-06-1396 |
ALCON INC / SYSTANE FREE LIQUID
GEL LUBRICANT EYE DROPS / VOLUNTARY RECALL /
DSCP 06-260 |
|
MMQC-06-1392 |
ABBOTT LABORATORIES / CLINICAL
CHEMISTRY PHENOBARBITAL / PRODUCT RECALL / DSCP
06--256 |
|
MMQC-06-1389 |
RITUXAN (RITUXIMAB) / FDA
MEDWATCH PUBLIC HEALTH ADVISORY |
|
MMQC-06-1388 |
BAYER PHARMACEUTICALS REVISIONS
TO PRESCRIBING INFORMATION FOR TRASYLOL (APROTININ)
/ FDA MEDWATCH |
|
MMQC-06-1387 |
SANOFI PASTEUR RESUMES ORDERING
OF ADACEL VACCINE / INFORMATION BULLETIN |
|
MMQC-06-1386 |
NOTICE OF CHANGE TO WARNING
SECTION OF LABEL FOR HEPARIN SODIUM INJECTION /
FDA MEDWATCH |
|
MMQC-06-1385 |
COMPOUNDED TOPICAL ANESTHETIC
CREAMS / FDA MEDWATCH PUBLIC HEALTH NOTICE |
|
MMQC-06-1384 |
WARNING AGAINST MANUFACTURING
UNAPPROVED DRUG PRODUCTS CONTAINING QUININE /
FDA MEDWATCH |
|
MMQC-06-1379 |
KAVO AMERICA CORP / QUATTROCARE
SPRAY / URGENT MEDICAL DEVICE RECALL / DSCP
06-250 |
|
MMQC-06-1374 |
THE UNITED STATES ARMY MEDICAL
MATERIEL AGENCY (USAMMA) MEDICAL LOGISTICS
MANAGEMENT INTERNSHIP PROGRAM (MLMIP) /
INFORMATION BULLETIN |
|
MMQC-06-1373 |
DOLOPHINE (METHADONE
HYDROCHLORIDE) / REPORTS OF DEATH, NARCOTIC
OVERDOSE, AND SERIOUS CARDIAC ARRHYTHMIAS /
MEDWATCH |
|
MMQC-06-1347 |
WYETH
EFFEXOR XR® (VENLAFAXINE HCL) EXTENDED-RELEASE
CAPSULES AND EFFEXOR® (VENLAFAXINE HCL) TABLETS
/ FDA MEDWATCH SAFETY NOTICE |
|
MMQC-06-1346 |
HEARTLAND
REPACK SERVICES / URGENT DRUG RECALL / MEDWATCH
|
|
MMQC-06-1344 |
FDA
UPDATES ITS NATIONWIDE ALERT ON COUNTERFEIT
BLOOD GLUCOSE TEST STRIPS / FDA NEWS
|
|
MMQC-06-1342 |
NOVARTIS
GLEEVEC® (IMATINIB MESYLATE) / FDA SAFETY
INFORMATION / MEDWATCH |
|
MMQC-06-1336 |
IMMEDIATE
MESSAGE / ROCHE DIAGNOSTICS COAGUCHEK® BRAND PT
TEST STRIPS / RECOMMENDED FDA CLASS I /
ADDITIONAL INFORMATION |
|
MMQC-06-1335 |
IMMEDIATE
MESSAGE / ROCHE DIAGNOSTICS COAGUCHEK BRAND PT
TEST STRIPS / RECOMMENDED FDA CLASS I / DSCP
06-219 |
|
MMQC-06-1329 |
COUNTERFEIT ONCE TOUCH TEST STRIPS / FDA
MEDWATCH |
|
MMQC-06-1328 |
EXUBERA
(INSULIN HUMAN [RDNA ORIGIN]) RISK OF DOSING
ERRORS / ALERT |
|
MMQC-06-1325 |
BAXTER
CONTINU-FLO SOLUTION SETS WITH NYPRO CHECK
VALVES / SAFETY ALERT / DSCP 06-207 |
|
MMQC-06-1323 |
HOSPIRA
PRECEDEX® (DEXMEDETOMIDINE HCL INJECTION) /
IMPORTANT DRUG RECALL / DSCP 06-204 |
|
MMQC-06-1322 |
ABBOTT
LABORATORIES VARIOUS SIMILAC LIQUID READY-TO-EAT
INFANT FORMULA IN 32-OUNCE PLASTIC BOTTLES AND
HOSPITAL DISCARGE KITS / NATIONWIDE RECALL/ DSCP
06-211
 |
|
MMQC-06-1321 |
MISADMINSTRATION OF MENINGOCOCCAL CONJUGATE
VACCINE / DEPARTMENT OF DEFENSE PATIENT SAFETY
CENTER ADVISORY |
|
MMQC-06-1320 |
PFIZER
SOLU-MEDROL® (METHYLPREDNISOLONE SODIUM
SUCCINATE) / IMPORTANT CORRECTION OF DRUG
INFORMATION |
|
MMQC-06-1319 |
SMALLPOX
VACCINE EXTENSION OF DATING FOR LOT 4030013
|
|
MMQC-06-1310 |
PRELIMINARY INFORMATION ON LAMICTAL® (LAMOTRIGINE)
/ FDA MEDWATCH |
|
MMQC-06-1309 |
TRASYLOL®
(APROTININ INJECTION) / FDA MEDWATCH SAFETY
ADVISORY |
|
MMQC-06-1308 |
GENENTECH
AVASTIN® (BEVACIZUMAB) / FDA MEDWATCH DRUG
WARNING |
|
MMQC-06-1307 |
RESULTS OF
STUDY USING ORTHO EVRA / FDA MEDWATCH
|
|
MMQC-06-1295 |
BD
MEDICAL 1ML SAFETYGLIDE? ALLERGY AND
TUBERCULIN SYRINGES / URGENT PRODUCT
RECALL / DSCP 06-181 |
|
MMQC-06-1289 |
SANOFI PASTEUR TEMPORARY SHORTAGE OF
ADACEL® VACCINE / UPDATED INFORMATION
BULLETIN |
|
MMQC-06-1288 |
DIETARY SUPPLEMENTS CONTAINING EPHEDRINE
ALKALOIDS / FDA MEDWATCH SAFETY
INFORMATION |
|
MMQC-06-1283 |
SANOFI PASTEUR TEMPORARY SHORTAGE OF
ADACEL® VACCINE / INFORMATION BULLETIN
|
|
August 2006 |
|
|
MMQC-06-1281 |
BAXTER / CHANGE IN RETURNED GOODS POLICY
/ INFORMATION ONLY |
|
MMQC-06-1276 |
HARDY DIAGNOSTICS / BHI AGAR WITH
VANCOMYCIN / QUALITY ASSURANCE RECALL /
DSCP 06-169 |
|
MMQC-06-1269 |
GLAXOSMITHKLINE / DEXEDRINE® (DEXTROAMPHETAMINE
SULFATE) / LABEL CHANGE / MEDWATCH
|
|
MMQC-06-1268 |
FDA WARNS THREE PHARMACIES TO STOP
MASS-PRODUCING UNAPPROVED INHALATION
DRUGS / FDA MEDWATCH NOTIFICATION
|
|
MMQC-06-1267 |
ABRAXIS PHARMACEUTICAL PRODUCTS /
FLUMAZENIL INJECTION / VOLUNTARY RECALL
/ DSCP 06-161 |
|
MMQC-06-1266 |
AMERICAN® REGENT NOVAPLUS® (HYDRALAZINE
HCL INJECTION) / VOLUNTARY RECALL / DSCP
06-173 |
|
MMQC-06-1260 |
KING PHARMACEUTICALS® / LEVOXYL® (LEVOTHYROXINE
SODIUM) / VOLUNTARY RECALL / DSCP 06-170
|
|
MMQC-06-1259 |
IVAX PHARMACEUTICALS HYDROXYZINE PAMOATE
/ URGENT DRUG RECALL / DSCP 06-171
|
|
MMQC-06-1258 |
IVAX PHARMACEUTICALS CILOSTAZOL TABLETS
/ URGENT DRUG RECALL / DSCP 06-172
|
|
July 2006 |
|
MMQC-06-1235 |
SANOFI PASTEUR /
DECAVAC® VACCINE (TETANUS & DIPHTHERIA TOXOID) /
AMERISOURCE BERGEN VOLUNTARY RECALL |
|
MMQC-06-1224 |
DESTRUCTION OF
EXPIRED ANTHRAX VACCINE LOT FAV104 |
|
MMQC-06-1223 |
SOLVAY
PHARMACEUTICALS MARINOL® (DRONABINOL) CAPSULES /
DRUG PRODUCT RECALL / DSCP 06-136 |
|
MMQC-06-1219 |
SANOFI PASTEUR
DECAVAC (DIPHTHERIA TOXOID, ADSORBED / TETANUS
TOXOID) / VOLUNTARY RECALL / DSCP 06-124
|
|
MMQC-06-1217 |
POINTE SCIENTIFIC
LIQUID GLUCOSE HEX REAGENT SETS / URGENT MEDICAL
DEVICE RECALL / DSCP 06-120 |
|
MMQC-06-1215 |
FDA WARNS
CONSUMERS AND HEALTHCARE PROVIDERS NOT TO USE
BISMACINE, ALSO KNOWN AS CHROMACINE / MEDWATCH
|
|
MMQC-06-1203 |
RISK IN TAKING
MEDICATIONS TOGETHER / MEDWATCH |
|
MMQC-06-1201 |
SELECTIVE
SEROTONIN REUPTAKE INHIBITORS (SSRIS) AND
TREATMENT CHALLENGES OF DEPRESSION IN PREGNANCY
/ MEDWATCH |
|
MMQC-06-1200 |
PROCAINAMIDE HCL
CAPSULES / VOLUNTARY RECALL / DSCP 06-109
|
|
MMQC-06-1199 |
DO NOT PURCHASE
OR CONSUME ZIMAXX, LIBIDUS, NEOPHASE, NASUTRA,
VIGOR-25, ACTRA-RX, OR 4EVERON, ILLEGAL DRUGS /
FDA MEDWATCH NOTICE WARNING: |
|
MMQC-06-1198 |
APTIVUS® (TIPRANAVIR)
/ IMPORTANT SAFETY INFORMATION / MEDWATCH
|
|
MMQC-06-1197 |
KETEK® (TELITHROMYCIN)
/ PRODUCT LABEL UPDATE / MEDWATCH |
|
MMQC-06-1192 |
SMALLPOX VACCINE
INFORMATION BULLETIN FOR LOT 4020071
|
|
MMQC-06-1191 |
EXUBERA /
MEDICATION SAFETY ALERT |
|
MMQC-06-1190 |
AZATHIOPRINE /
ROXANE LABS / VOLUNTARY RECALL / DSCP 06-137
|
|
MMQC-06-1186 |
IMMEDIATE MESSAGE
/ NOVARTIS TRIAMINIC® VAPOR PATCH / FDA CLASS I
RECALL / DSCP 06-119 |
|
June 2006 |
|
|
MMQC-06-1185 |
SMALLPOX VACCINE
EXTENSION OF DATING FOR LOT 4030013 |
|
MMQC-06-1184 |
SMALLPOX VACCINE
EXTENSION OF DATING FOR VARIOUS LOTS
|
|
MMQC-06-1180 |
2005/2006
INFLUENZA VIRUS VACCINE / DISPOSITION
INSTRUCTIONS / DESTROY |
|
MMQC-06-1179 |
ANTHRAX VACCINE
EXPIRATION 90-DAY NOTICE LOT FAV107 |
|
MMQC-06-1178 |
WESTCORT®
(HYDROCORTISONE VALERATE) AND APOTHECON®
(HYDROCORTISONE VALERATE GENERIC) /
BRISTOL-MYERS SQUIBB / QUALITY ASSURANCE RECALL
/ DSCP 06-100 |
|
MMQC-06-1177 |
ABBOTT FREESTYLE
FLASH® BLOOD GLUCOSE METER AND FREESTYLE® BLOOD
GLUCOSE METER / URGENT MEDICAL DEVICE CORRECTION
/ DSCP 06-096
 |
|
MMQC-06-1174 |
BOCA INSULIN
SYRINGE / VOLUNTARY RECALL / DSCP 06-091
|
|
MMQC-06-1172 |
MOBIC®
(MELOXICAM) / BOEHR INGELHEIM PHARMACEUTICALS /
QUALITY ASSURANCE RECALL / DSCP 06-094
|
|
MMQC-06-1167 |
BAUSCH & LOMB /
RENU® WITH MOISTURELOC® CONTACT LENS SOLUTION /
QUALITY ASSURANCE RECALL / DSCP 06-060 (UPDATE)
|
|
MMQC-06-1166 |
DESTRUCTION OF
EXPIRED ANTHRAX VACCINE LOT FAV101 |
|
MMQC-06-1164 |
MERCK & CO. /
GARDASIL FDA LICENSES / FDA NEWS |