{"id":394047,"date":"2026-03-19T23:52:12","date_gmt":"2026-03-19T23:52:12","guid":{"rendered":"https:\/\/www.europesays.com\/ie\/394047\/"},"modified":"2026-03-19T23:52:12","modified_gmt":"2026-03-19T23:52:12","slug":"nearly-90000-bottles-of-childrens-oral-ibuprofen-recalled-fda-nbc-chicago","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/ie\/394047\/","title":{"rendered":"Nearly 90,000 bottles of children\u2019s oral Ibuprofen recalled FDA \u2013 NBC Chicago"},"content":{"rendered":"<p>Nearly 90,000 bottles of children&#8217;s oral Ibuprofen medicine have been recalled, according to <a href=\"https:\/\/www.accessdata.fda.gov\/scripts\/ires\/index.cfm?Product=218947\" target=\"_blank\" rel=\"noreferrer noopener nofollow\">a Food and Drug Administration report<\/a>, with health officials saying the medicine could contain a foreign substance.<\/p>\n<p>Pharmaceutical company Strides Pharma Inc. issued the voluntary recall March 2 because the firm received complaints &#8220;for a gel-like mass and black particles in the product,&#8221; the report said. <\/p>\n<p>March 16, the FDA classified the recall as Level II, which identifies it a situation where exposure to the product could have temporary adverse health impacts. <\/p>\n<p>According to the report, 89,592 bottles of Children&#8217;s Ibuprofen Oral Suspension, USP, 100 mg per 5 mL were recalled. The 4 fl. oz. bottles were manufactured by Taro Pharmaceuticals, the report said, and distributed to retailers nationwide. <\/p>\n<p>Lot numbers for the recalled products, with an expiration date of Jan. 31, 2027, can be found below:<\/p>\n<p>It wasn&#8217;t immediately clear how many complaints were received or if there were any reports of injuries. Photos of what the medication looks like were not provided.<\/p>\n<p>As of the time of publication, Strides Pharma had not responded to NBC Chicago&#8217;s request for comment. <\/p>\n","protected":false},"excerpt":{"rendered":"Nearly 90,000 bottles of children&#8217;s oral Ibuprofen medicine have been recalled, according to a Food and Drug Administration&hellip;\n","protected":false},"author":2,"featured_media":394048,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[274],"tags":[18,135,19,17,462,84929],"class_list":{"0":"post-394047","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-medication","8":"tag-eire","9":"tag-health","10":"tag-ie","11":"tag-ireland","12":"tag-medication","13":"tag-recalls"},"share_on_mastodon":{"url":"https:\/\/pubeurope.com\/@ie\/116258534071228910","error":""},"_links":{"self":[{"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/posts\/394047","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/comments?post=394047"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/posts\/394047\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/media\/394048"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/media?parent=394047"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/categories?post=394047"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/tags?post=394047"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}