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<rss version="2.0"><channel><title>Recalls Latest Topics</title><link>https://bmetgalaxy.com/forums/index.php?/forum/23-recalls/</link><description>Recalls Latest Topics</description><language>en</language><item><title>Wound and Burn Dressing Recall: Integra LifeSciences Removes Certain MediHoney and CVS Wound and Burn Products</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1240-wound-and-burn-dressing-recall-integra-lifesciences-removes-certain-medihoney-and-cvs-wound-and-burn-products/</link><description><![CDATA[Integra is removing certain Wound and Burn Dressing products that may have breached sterile barriers.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/wound-and-burn-dressing-recall-integra-lifesciences-removes-certain-medihoney-and-cvs-wound-and-burn" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1240</guid><pubDate>Fri, 06 Mar 2026 05:00:00 +0000</pubDate></item><item><title>Catheter Recall Expansion: Medline Industries Removes Reprocessed Electrophysiology and Ultrasound Catheters</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1242-catheter-recall-expansion-medline-industries-removes-reprocessed-electrophysiology-and-ultrasound-catheters/</link><description><![CDATA[Certain reprocessed catheters may contain residual particulates that could cause infection, embolism, or thrombosis<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/catheter-recall-expansion-medline-industries-removes-reprocessed-electrophysiology-and-ultrasound" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1242</guid><pubDate>Thu, 05 Mar 2026 05:00:00 +0000</pubDate></item><item><title>Catheter Recall: Medline Industries Removes Reprocessed Electrophysiology and Ultrasound Catheters</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1241-catheter-recall-medline-industries-removes-reprocessed-electrophysiology-and-ultrasound-catheters/</link><description><![CDATA[Certain reprocessed catheters may contain residual particulates that could cause infection, embolism, or thrombosis.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/catheter-recall-medline-industries-removes-reprocessed-electrophysiology-and-ultrasound-catheters" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1241</guid><pubDate>Thu, 05 Mar 2026 05:00:00 +0000</pubDate></item><item><title>Stent Recall: Boston Scientific Removes Certain AXIOS Stents and Electrocautery-Enhanced Delivery Systems</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1219-stent-recall-boston-scientific-removes-certain-axios-stents-and-electrocautery-enhanced-delivery-systems/</link><description><![CDATA[Boston Scientific is removing certain stents and delivery systems due to issues with deployment and expansion.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/stent-recall-boston-scientific-removes-certain-axios-stents-and-electrocautery-enhanced-delivery" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1219</guid><pubDate>Wed, 25 Feb 2026 05:00:00 +0000</pubDate></item><item><title>Early Alert: Heart Pump Purge Cassette Issue from Abiomed</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1218-early-alert-heart-pump-purge-cassette-issue-from-abiomed/</link><description><![CDATA[Impella Generation 1 Purge Cassettes have an increased risk of purge leaks. Purge leaks can lead to low pump pressure and pump stops<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-heart-pump-purge-cassette-issue-abiomed" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1218</guid><pubDate>Wed, 25 Feb 2026 05:00:00 +0000</pubDate></item><item><title>Infusion Pump Software Correction: Fresenius Kabi Issues Correction for Ivenix Large Volume Pump Software</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1217-infusion-pump-software-correction-fresenius-kabi-issues-correction-for-ivenix-large-volume-pump-software/</link><description><![CDATA[Fresenius Kabi is correcting Ivenix LVP software due to anomalies that could cause serious patient harm or death<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/infusion-pump-software-correction-fresenius-kabi-issues-correction-ivenix-large-volume-pump-software" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1217</guid><pubDate>Wed, 25 Feb 2026 05:00:00 +0000</pubDate></item><item><title>Insufflation Unit Recall: Olympus Removes High Flow Insufflation Units</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1193-insufflation-unit-recall-olympus-removes-high-flow-insufflation-units/</link><description><![CDATA[ Olympus is removing certain High Flow Insufflation Unit models due to software issues that may lead to overpressure events.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/insufflation-unit-recall-olympus-removes-high-flow-insufflation-units" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1193</guid><pubDate>Mon, 23 Feb 2026 05:00:00 +0000</pubDate></item><item><title>Early Alert: Trividia Health Issues Correction for TRUE METRIX Blood Glucose Monitoring Systems  </title><link>https://bmetgalaxy.com/forums/index.php?/topic/1170-early-alert-trividia-health-issues-correction-for-true-metrix-blood-glucose-monitoring-systems/</link><description><![CDATA[Trividia recommends that device users who receive an E-5 error code and are experiencing symptoms of high glucose should seek medical care immediately   <p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-trividia-health-issues-correction-true-metrix-blood-glucose-monitoring-systems" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1170</guid><pubDate>Tue, 17 Feb 2026 05:00:00 +0000</pubDate></item><item><title>Electronic Homecare Bed Correction: Medline Updates Use Instructions for Homecare Beds</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1171-electronic-homecare-bed-correction-medline-updates-use-instructions-for-homecare-beds/</link><description><![CDATA[Medline updates use instructions for Electronic Homecare Beds due to risk of electrical fires and entrapment.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/electronic-homecare-bed-correction-medline-updates-use-instructions-homecare-beds" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1171</guid><pubDate>Fri, 13 Feb 2026 05:00:00 +0000</pubDate></item><item><title>Emergency Response Safety Kit Recall: Airlife Removes Certain Broselow Pediatric Emergency Rainbow Tapes and Broselow ALS Organizers</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1152-emergency-response-safety-kit-recall-airlife-removes-certain-broselow-pediatric-emergency-rainbow-tapes-and-broselow-als-organizers/</link><description><![CDATA[AirLife is removing Broselow Rainbow Tapes due to incorrectly printed medication dosing information. <p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/emergency-response-safety-kit-recall-airlife-removes-certain-broselow-pediatric-emergency-rainbow" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1152</guid><pubDate>Wed, 11 Feb 2026 05:00:00 +0000</pubDate></item><item><title>Trividia Health, Inc. Initiates Labeling Correction for all TRUE METRIX&#xAE; Blood Glucose Monitoring Systems </title><link>https://bmetgalaxy.com/forums/index.php?/topic/1147-trividia-health-inc-initiates-labeling-correction-for-all-true-metrix%C2%AE-blood-glucose-monitoring-systems/</link><description><![CDATA[FT. LAUDERDALE, FL) – February 6, 2026 – Trividia Health, Inc., announced today that it is initiating a labeling correction which requires a modification of the Owner’s Booklets/System Instructions for Use for all TRUE METRIX, TRUE METRIX AIR, TRUE METRIX GO, and TRUE METRIX PRO Blood Glucose Monit<p><a href="http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/trividia-health-inc-initiates-labeling-correction-all-true-metrixr-blood-glucose-monitoring-systems" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1147</guid><pubDate>Fri, 06 Feb 2026 05:00:00 +0000</pubDate></item><item><title><![CDATA[Detachable Coil System Recall: J&J MedTech/CERENOVUS Inc. Remove CEREPAK Detachable Coil System]]></title><link>https://bmetgalaxy.com/forums/index.php?/topic/1148-detachable-coil-system-recall-jj-medtechcerenovus-inc-remove-cerepak-detachable-coil-system/</link><description><![CDATA[MedTech/CERENOVUS is removing CEREPAK Detachable Coil Systems due to a higher than expected failure to detach rate<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/detachable-coil-system-recall-jj-medtechcerenovus-inc-remove-cerepak-detachable-coil-system" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1148</guid><pubDate>Thu, 05 Feb 2026 05:00:00 +0000</pubDate></item><item><title>Glucose Monitor Sensor Recall: Abbott Diabetes Care Removes Certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus Sensors</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1114-glucose-monitor-sensor-recall-abbott-diabetes-care-removes-certain-freestyle-libre-3-and-freestyle-libre-3-plus-sensors/</link><description><![CDATA[Certain Abbott Diabetes Care Continuous Glucose Monitor sensors may incorrect or lower than actual glucose readings<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/glucose-monitor-sensor-recall-abbott-diabetes-care-removes-certain-freestyle-libre-3-and-freestyle" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1114</guid><pubDate>Thu, 05 Feb 2026 05:00:00 +0000</pubDate></item><item><title>Early Alert: Heart Pump Issue from Abiomed</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1115-early-alert-heart-pump-issue-from-abiomed/</link><description><![CDATA[The differential pressure sensor in certain Impella devices may malfunction and cause sensor values to drift. <p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-heart-pump-issue-abiomed" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1115</guid><pubDate>Tue, 03 Feb 2026 05:00:00 +0000</pubDate></item><item><title>casino vavada &#x440;&#x430;&#x431;&#x43E;&#x447;&#x435;&#x435; &#x437;&#x435;&#x440;&#x43A;&#x430;&#x43B;&#x43E;</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1093-casino-vavada-%D1%80%D0%B0%D0%B1%D0%BE%D1%87%D0%B5%D0%B5-%D0%B7%D0%B5%D1%80%D0%BA%D0%B0%D0%BB%D0%BE/</link><description><![CDATA[Для бесперебойного доступа к casino vavada (вавада), просто перейдите по ссылке [url=https://ladykrasotka.com/]casino vavada зеркало[/url] и начните игру! <br />
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Оно открывает двери к миру развлечений Vavada .]]></description><guid isPermaLink="false">1093</guid><pubDate>Sat, 31 Jan 2026 08:43:21 +0000</pubDate></item><item><title>Early Alert: Insufflation Unit Issue from Olympus</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1063-early-alert-insufflation-unit-issue-from-olympus/</link><description><![CDATA[Olympus is removing certain High Flow Insufflation Unit models due to software issues that may lead to overpressure events.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-insufflation-unit-issue-olympus" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1063</guid><pubDate>Thu, 22 Jan 2026 05:00:00 +0000</pubDate></item><item><title>Early Alert: Wound and Burn Dressing Issue from Integra LifeSciences</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1062-early-alert-wound-and-burn-dressing-issue-from-integra-lifesciences/</link><description><![CDATA[Integra is removing all MediHoney Wound and Burn products and certain lots of CVS Wound Gel that may have breached sterile barriers<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-wound-and-burn-dressing-issue-integra-lifesciences" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1062</guid><pubDate>Thu, 22 Jan 2026 05:00:00 +0000</pubDate></item><item><title>Anesthetic Vaporizer Recall: Draeger Removes Vapor 2000 and Vapor 3000 Vaporizers </title><link>https://bmetgalaxy.com/forums/index.php?/topic/1017-anesthetic-vaporizer-recall-draeger-removes-vapor-2000-and-vapor-3000-vaporizers/</link><description><![CDATA[Draeger is removing certain Vapor 2000 and Vapor 3000 Vaporizers due to impurities found within a component.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/anesthetic-vaporizer-recall-draeger-removes-vapor-2000-and-vapor-3000-vaporizers" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1017</guid><pubDate>Fri, 16 Jan 2026 05:00:00 +0000</pubDate></item><item><title>Early Alert: Broselow Rainbow Tape Issue from AirLife</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1016-early-alert-broselow-rainbow-tape-issue-from-airlife/</link><description><![CDATA[AirLife is removing Broselow Rainbow Tapes due to incorrectly printed medication dosing information. <p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-broselow-rainbow-tape-issue-airlife" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1016</guid><pubDate>Fri, 16 Jan 2026 05:00:00 +0000</pubDate></item><item><title>Olympus Expands Voluntary Recall for ViziShot 2 FLEX (19G) EBUS -TBNA Needles</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1015-olympus-expands-voluntary-recall-for-vizishot-2-flex-19g-ebus-tbna-needles/</link><description><![CDATA[CENTER VALLEY, Pa., (January 16, 2026)  — Olympus Corporation has announced the expansion of a previous global medical device removal action for ViziShot 2 FLEX (19G) EBUS -TBNA needles (“ViziShot 2 FLEX”) after receiving and investigating complaints of device components ejecting or detaching during<p><a href="http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/olympus-expands-voluntary-recall-vizishot-2-flex-19g-ebus-tbna-needles" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1015</guid><pubDate>Fri, 16 Jan 2026 05:00:00 +0000</pubDate></item><item><title>Early Alert: Stent and Electrocautery-Enhanced Delivery System Issue from Boston Scientific</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1014-early-alert-stent-and-electrocautery-enhanced-delivery-system-issue-from-boston-scientific/</link><description><![CDATA[Boston Scientific is removing certain stents and delivery systems due to issues with deployment and expansion.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-stent-and-electrocautery-enhanced-delivery-system-issue-boston-scientific" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1014</guid><pubDate>Fri, 16 Jan 2026 05:00:00 +0000</pubDate></item><item><title>Anesthesia Kit Recall: Medline Removes Anesthesia Circuits and Anesthesia Circuit Kits</title><link>https://bmetgalaxy.com/forums/index.php?/topic/1013-anesthesia-kit-recall-medline-removes-anesthesia-circuits-and-anesthesia-circuit-kits/</link><description><![CDATA[Medline is removing certain anesthesia circuit kits due to cracks and leaks in the tubing.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/anesthesia-kit-recall-medline-removes-anesthesia-circuits-and-anesthesia-circuit-kits" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1013</guid><pubDate>Fri, 16 Jan 2026 05:00:00 +0000</pubDate></item><item><title>Abbott Initiates Medical Device Correction for Certain  FreeStyle Libre&#xAE; 3 and FreeStyle Libre 3 Plus Sensors in the U.S. </title><link>https://bmetgalaxy.com/forums/index.php?/topic/1018-abbott-initiates-medical-device-correction-for-certain-freestyle-libre%C2%AE-3-and-freestyle-libre-3-plus-sensors-in-the-us/</link><description><![CDATA[ABBOTT PARK, Ill., Nov. 24, 2025 — Abbott has initiated a medical device correction for certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors in the United States after internal testing determined that some sensors may provide incorrect low glucose readings.  <p><a href="http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/abbott-initiates-medical-device-correction-certain-freestyle-librer-3-and-freestyle-libre-3-plus" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">1018</guid><pubDate>Thu, 15 Jan 2026 05:00:00 +0000</pubDate></item><item><title>Early Alert: Dialysis Tubing Set Issue from Vantive</title><link>https://bmetgalaxy.com/forums/index.php?/topic/989-early-alert-dialysis-tubing-set-issue-from-vantive/</link><description><![CDATA[Prismaflex Set deaeration chambers may dislodge from the Prismaflex Control Unit during use. <p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-dialysis-tubing-set-issue-vantive" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">989</guid><pubDate>Wed, 14 Jan 2026 05:00:00 +0000</pubDate></item><item><title>Organ Recovery Pack Correction: AVID Medical Issues Correction for Medical Convenience and Organ Recovery Kits</title><link>https://bmetgalaxy.com/forums/index.php?/topic/992-organ-recovery-pack-correction-avid-medical-issues-correction-for-medical-convenience-and-organ-recovery-kits/</link><description><![CDATA[AVID is removing bags from Organ Recovery and Medical Convenience Kits due to the bags being made of non-medical grade Poly and lacking intact seals.<p><a href="http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/organ-recovery-pack-correction-avid-medical-issues-correction-medical-convenience-and-organ-recovery" rel="external nofollow">View the full article</a></p>]]></description><guid isPermaLink="false">992</guid><pubDate>Fri, 09 Jan 2026 05:00:00 +0000</pubDate></item></channel></rss>
