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This page shows you the most recent publications within this specialty of the MedWorm directory.

Quasar Bio-Tech, Inc. dba Silver Bay LLC - Quasar Power Pack - Class 2 Recall
Quasar Power Pack contains a Baby Quasar and a Baby Blue. The Baby Quasar is an infrared LED lamp. The Baby Blue uses blue LED light to be used in combination with the Baby Quasar to treat acne. The Quasar Power Pack is labeled in part: "***BABY QUASAR & BABY BLUE***QUASAR POWERPACK***FOR YOUTHFUL, RADIANT, CLEAR SKIN***SKIN REJUVENATING SYSTEM WITH SEQUEPULSE PLUS ADVANCED ACNE CLARIFYING SYSTEM***Manufactured by: Quasar Biotech, Inc., BPP101 LAB-003-E, ***Made in the USA with highest quality components and durable aluminum. Five Year Warranty.***" (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 12, 2012 Category: Medical Equipment Source Type: alerts

Clark Laboratories, Inc. (dba,Trinity Biotech USA) - Captia VZV IgG - Class 3 Recall
Trinity Biotech, Captia VZV IgG. Product code 2325600: 96 Tests; product code: 2325601: 480 tests. For in vitro diagnostic use. Intended for the detection and quantitative determination of IgG antibody to VZV in human sera. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 24, 2012 Category: Medical Equipment Source Type: alerts

Tcoag Us, Incorporated - Minutex DDimer - Class 2 Recall
Minutex D-Dimer ; Trinity Biotech plc, Bray, Co. Wicklow, Ireland. Tel: (353) 1 276 9800, Fax: (353) 1 276 9888, Web: www.trinitybiotech.com Minutex D-Dimer is a latex agglutination test for semiquantitative determination of fibrin D-Dimer. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 7, 2011 Category: Medical Equipment Source Type: alerts

Stryker Biotech - Class 2 Recall
Stryker Biotech OP-1 Putty (OP-1, BMP-7, bone morphogenetic protein) "Catalog numbers: 300-50, 300-55 OP-1 Putty is authorized by Federal law for use as an alternative to autograft in compromised patients requiring revision posterolateral (intertransverse) lumbar spinal fusion, for whom autologous bone and bone marrow harvest are not feasible or are not expected to promote fusion. Examples of compromising factors include osteoporosis, smoking and diabetes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 18, 2011 Category: Medical Equipment Source Type: alerts

Bio-Rad Laboratories Inc - Autoimmune EIA ANA Screening Kit - Class 2 Recall
Bio Rad brand Autoimmune EIA ANA Screening Kit, 96 Tests, Catalog No. 96AN-BPU-TRINITY. Manufactured by: Bio-Rad Laboratories, Inc. Hercules, CA and distributed by Trinity Biotech, USA. Intended to screen for the presence of antinuclear antibodies (ANAs) in human serum as an aid in the diagnosis of certain rheumatic diseases. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 2, 2011 Category: Medical Equipment Source Type: alerts

Stryker Charged with Marketing Fraud
Stryker Corp.'s biotech division and four current and former executives have been indicted on federal fraud charges related to their marketing of two bone-growth products. (Source: MedPage Today Product Alert)
Source: MedPage Today Product Alert - October 29, 2009 Category: Drugs & Pharmacology Source Type: alerts

First Swine Flu Vaccine Trials Begin in Australia
LITTLE FALLS, N.J. (MedPage Today) -- Two biotechnology companies in Australia have begun the first human trials of a vaccine for the 2009 H1N1 (swine flu) virus, according to media reports. (Source: MedPage Today Product Alert)
Source: MedPage Today Product Alert - July 22, 2009 Category: Drugs & Pharmacology Source Type: alerts

Stryker Biotech - Class 3 Recall
Stryker Biotech OP- 1 Implant is indicated for use as an alternative to autograft in recalcitrant long bone nonunions where use of autograft is unfeasible and alternative treatments have failed. Catalog Number: 100-25 (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - September 20, 2008 Category: Medical Equipment Source Type: alerts

Applied Biotech Inc - Clearview hCG Combo - Class 2 Recall
Clearview hCG Combo Waived for urine & Moderate for serum, Wampole Laboratories, ABI List No/Product No. 6026KCV; Contents 30 Individually pouched test cassettes with disposable pipettes, 1 Directional Insert; Inverness Medical Professional Diagnostics Group; Marketed by Wampole Laboratories, 2 Research Way, Princeton NJ 08540 USA (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - November 21, 2007 Category: Medical Equipment Source Type: alerts

Applied Biotech Inc - Clearview hCG Combo with Reference Line - Class 2 Recall
Clearview hCG Combo with Reference Line, Wampole Laboratories, ABI List No/Product No. 6028KCV; 30 Individually pouched test cassettes with disposable pipettes, 1 Directional Insert; Inverness Medical Professional Diagnostics Group; Marketed by Wampole Laboratories, 2 Research Way, Princeton NJ 08540 USA (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - November 21, 2007 Category: Medical Equipment Source Type: alerts

Integra Biotechnical LLC - ProWick Shoulder Postoperative Dressing and Cold Therapy System - Class 2 Recall
ProWick Shoulder Postoperative Dressing and Cold Therapy System, Model number AR-1625 (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - April 4, 2007 Category: Medical Equipment Source Type: alerts

Stryker Biotech - Calstrux¿ - Class 2 Recall
Calstrux¿ (Previously known as TCP Putty)- Absorbable Bone Void Filler, packaged in: Catalog Number: 400-05: quantity-5cc Catalog Number: 400-10: quantity 10cc Catalog Number: 400-15: quantity 15cc (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - December 14, 2006 Category: Medical Equipment Source Type: alerts

Applied Biotech Inc - Medplus ER Drug Screen Test - Class 2 Recall
Medplus ER Drug Screen Test Model #5800KAB packaged as 25 individually pouched devices in a labeled kit box. (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - August 7, 2006 Category: Medical Equipment Source Type: alerts

Applied Biotech Inc - Signify hCG Serum/Urine 30 Test Kit - Class 2 Recall
Signify hCG Serum/Urine 30 Test Kit, Abbott List No. 07K09-30, ABI List No. 6026KSI, Lot# 84936, Exp 02/10/2007 (Source: Medical Device Recalls since July 07, 2006)
Source: Medical Device Recalls since July 07, 2006 - June 9, 2006 Category: Medical Equipment Source Type: alerts