{"id":7664,"date":"2023-03-08T12:58:23","date_gmt":"2023-03-08T09:58:23","guid":{"rendered":"https:\/\/urbancare.clinic\/eyedrops-recall-some-brands-may-not-be-sterile-says-fda\/"},"modified":"2023-03-08T12:58:23","modified_gmt":"2023-03-08T09:58:23","slug":"augentropfen-erinnern-daran-dass-einige-marken-moglicherweise-nicht-steril-sind-sagt-die-fda","status":"publish","type":"post","link":"https:\/\/urbancare.clinic\/de\/augentropfen-erinnern-daran-dass-einige-marken-moglicherweise-nicht-steril-sind-sagt-die-fda\/","title":{"rendered":"R\u00fcckruf von Augentropfen: Einige Marken sind m\u00f6glicherweise nicht steril, sagt die FDA"},"content":{"rendered":"<div><img decoding=\"async\" src=\"https:\/\/urbancare.clinic\/wp-content\/uploads\/2023\/03\/eyedrops-recall-some-brands-may-not-be-sterile-says-fda.jpg\" class=\"ff-og-image-inserted\" style=\"display:none\"><\/div>\n<p>Die Food and Drug Administration (FDA) hat mehrere R\u00fcckrufmitteilungen f\u00fcr zwei Marken von Augentropfen herausgegeben, die m\u00f6glicherweise nicht steril sind und zu erheblichen Sehst\u00f6rungen und schweren Verletzungen f\u00fchren k\u00f6nnen.<\/p>\n<p>Der R\u00fcckruf betrifft bestimmte Augentropfen, die von Pharmedica und Apotex vertrieben werden, und folgt auf einen R\u00fcckruf im Februar, der mit einem in Verbindung gebracht wurde&nbsp;<a href=\"https:\/\/www.cdc.gov\/hai\/outbreaks\/CRPA-artificial-tears.html#anchor_1674746879046\" rel=\"nofollow noopener\" target=\"_blank\">Ausbruch in mehreren Staaten<\/a>&nbsp;von arzneimittelresistenten Infektionen. Dieser Ausbruch verursachte den Tod einer Person und hinterlie\u00df bei mindestens f\u00fcnf weiteren Personen einen dauerhaften Sehverlust&nbsp;<a href=\"https:\/\/abcnews.go.com\/Business\/wireStory\/fda-eyedrops-brands-recalled-due-risks-97684402\" rel=\"nofollow noopener\" target=\"_blank\">abc Nachrichten<\/a>.<\/p>\n<p>W\u00e4hrend bei den zuletzt zur\u00fcckgerufenen Produkten keine Verletzungen oder Krankheiten gemeldet wurden, \u201eerh\u00f6ht die Verwendung kontaminierter k\u00fcnstlicher Tr\u00e4nen das Risiko von Augeninfektionen, die zur Erblindung oder zum Tod f\u00fchren k\u00f6nnen\u201c, sagt der&nbsp;<a href=\"https:\/\/www.fda.gov\/safety\/recalls-market-withdrawals-safety-alerts\/pharmedica-usa-llc-issues-voluntary-worldwide-recall-purely-soothing-15-msm-drops-due-non-sterility\" rel=\"nofollow noopener\" target=\"_blank\">FDA<\/a>.<\/p>\n<p>Sowohl Pharmedica als auch Apotex gaben an, dass sie im Zusammenhang mit Gespr\u00e4chen mit der FDA freiwillig mehrere Chargen ihrer Produkte vom Markt nehmen w\u00fcrden.<\/p>\n<div id=\"dfp-ad-oop2\" class=\"dfp-tag-wrapper\"> <\/div>\n<p>Mit Sitz in Arizona, Pharmedica&#039;s&nbsp;<a href=\"https:\/\/www.fda.gov\/safety\/recalls-market-withdrawals-safety-alerts\/pharmedica-usa-llc-issues-voluntary-worldwide-recall-purely-soothing-15-msm-drops-due-non-sterility\" rel=\"nofollow noopener\" target=\"_blank\">abrufen<\/a>&nbsp;ist f\u00fcr zwei Chargen seiner \u201ePurely Soothing 15% MSM Drops\u201c, rezeptfreie Tropfen zur Behandlung allgemeiner Reizungen. Das Unternehmen fordert die Verbraucher dringend auf, die Verwendung des Arzneimittels aufgrund von Unsterilit\u00e4tsproblemen, die \u201ezur Erblindung f\u00fchren k\u00f6nnten\u201c, sofort einzustellen.<\/p>\n<p>Der R\u00fcckruf betrifft fast 2.900 Flaschen, die \u201e\u00fcber Online-E-Commerce und Messen (z. B.&nbsp;<a data-sys=\"1\" href=\"https:\/\/www.ibtimes.com\/company\/amazon\" rel=\"nofollow noopener\" target=\"_blank\">Amazonas<\/a>&nbsp;Marktplatz usw.).\u201c<\/p>\n<p>Der Apotex&nbsp;<a href=\"https:\/\/www.fda.gov\/safety\/recalls-market-withdrawals-safety-alerts\/apotex-corp-issues-voluntary-nationwide-recall-brimonidine-tartrate-ophthalmic-solution-015-due\" rel=\"nofollow noopener\" target=\"_blank\">abrufen<\/a>&nbsp;ist f\u00fcr sechs Chargen \u201eBrimonidintartrat-Augenl\u00f6sung, 0,151 TP3T\u201c, bei denen es sich um verschreibungspflichtige Augentropfen handelt, die haupts\u00e4chlich zur Behandlung einer Form des Glaukoms eingesetzt werden. Die betroffenen Produkte seien zwischen April 2022 und Februar dieses Jahres verkauft worden, teilte das Unternehmen mit.<\/p>\n<p>Apotex mit Sitz in Florida sagt, die Mitteilung sei \u201eaus gro\u00dfer Vorsicht initiiert worden, da sich in einigen Deckeln der Einheiten Risse gebildet haben\u201c, die \u201edie Sterilit\u00e4t und, wenn ja, die M\u00f6glichkeit unerw\u00fcnschter Ereignisse beeintr\u00e4chtigen k\u00f6nnten\u201c.<\/p>\n<p>Beide Unternehmen fordern Gro\u00df- und Einzelh\u00e4ndler auf, den Vertrieb der zur\u00fcckgerufenen Produkte einzustellen und raten allen Verbrauchern, die m\u00f6glicherweise die kontaminierten Tropfen verwendet haben, bei Auftreten von Symptomen einen Arzt aufzusuchen.<\/p>\n<p><a href=\"https:\/\/www.medicaldaily.com\/eyedrops-recall-some-brands-may-not-be-sterile-says-fda-468376?utm_source=Public&#038;utm_medium=Feed&#038;utm_campaign=Distribution\">Medizinische t\u00e4gliche Quelle<\/a><\/p>\n<p>","protected":false},"excerpt":{"rendered":"<p>Der R\u00fcckruf betrifft fast 2.900 Flaschen, die \u201e\u00fcber Online-E-Commerce und Messen (z. B. Amazon Marketplace usw.)\u201c vertrieben wurden.<\/p>","protected":false},"author":2,"featured_media":7665,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"Default","format":"standard","meta":{"fifu_image_url":"https:\/\/urbancare.clinic\/wp-content\/uploads\/2023\/03\/eyedrops-recall-some-brands-may-not-be-sterile-says-fda.jpg","fifu_image_alt":"","footnotes":""},"categories":[27],"tags":[],"class_list":["post-7664","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.6 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Eyedrops Recall: Some Brands May Not Be Sterile, Says FDA - Urban Care Clinic<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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