FDA and CPSC Product Recall Tracker
175
June 2026
Regulation
Product recalls announced by the US Food and Drug Administration and the Consumer Product Safety Commission, confirmed each month from regulatory portals, company press releases, and news sources. Covered event types include food safety recalls, drug and biologic recalls, medical device recalls, and consumer product safety recalls. Each record includes the product name, recalling company, recall reason, affected lot numbers or quantities, and announcement date. The May 2026 edition reviewed 2,436 candidate sources and confirmed 389 validated events.
FDA food drug or medical device recall or CPSC consumer product safety recall announced
Retailers and distributors use it to identify recalled products in their supply chain before consumer complaints arise. Regulatory affairs and quality teams at food, pharma, and consumer goods companies use it to benchmark recall frequency and monitor competitor compliance events. Product liability and insurance teams use it as a structured record of confirmed recall actions. Food safety journalists and consumer advocacy organisations track recall activity through it.
1309
<table class="catchall-table"><thead><tr><th style="min-width:40px">#</th><th style="min-width:280px">Event</th><th style="min-width:160px">Recall Date</th><th style="min-width:160px">Recalling Company</th><th style="min-width:160px">Affected Regions</th><th style="min-width:160px">Recall Classification</th><th style="min-width:160px">Recall Agency</th><th style="min-width:160px">Recall Reason</th><th style="min-width:160px">Product Name</th><th style="min-width:160px">Recall Category</th><th style="min-width:160px">Units Affected</th></tr></thead><tbody><tr><td style="min-width:40px">1</td><td style="min-width:280px">Blood Pressure Medication Recall by Rising Pharma Holdings</td><td style="min-width:160px">2026-06-24</td><td style="min-width:160px">Rising Pharma Holdings Inc. of New Jersey</td><td style="min-width:160px">nationwide (United States)</td><td style="min-width:160px">Class II</td><td style="min-width:160px">FDA</td><td style="min-width:160px">manufacturing issue</td><td style="min-width:160px">Blood pressure medication (100-count and 1,000-count bottles)</td><td style="min-width:160px">Drug</td><td style="min-width:160px">1,000,000</td></tr><tr><td style="min-width:40px">2</td><td style="min-width:280px">FDA Recalls Alyacen Birth Control Dosages Nationwide</td><td style="min-width:160px">2026-06-12</td><td style="min-width:160px">Glenmark Pharmaceuticals</td><td style="min-width:160px">nationwide</td><td style="min-width:160px">Class II</td><td style="min-width:160px">FDA</td><td style="min-width:160px">failed quality standards related to impurities and degradation products</td><td style="min-width:160px">Alyacen 7/7/7 tablets</td><td style="min-width:160px">Drug</td><td style="min-width:160px">27,000</td></tr><tr><td style="min-width:40px">3</td><td style="min-width:280px">Inventia Healthcare Recalls Chlorthalidone Tablets</td><td style="min-width:160px">2026-06-05</td><td style="min-width:160px">Inventia Healthcare Limited</td><td style="min-width:160px">nationwide</td><td style="min-width:160px">Class II</td><td style="min-width:160px">FDA</td><td style="min-width:160px">failed dissolution specifications</td><td style="min-width:160px">Chlorthalidone Tablets, USP, 25 mg</td><td style="min-width:160px">Drug</td><td style="min-width:160px">11,400</td></tr><tr><td style="min-width:40px">4</td><td style="min-width:280px">FDA Recalls Heart and Kidney Medications</td><td style="min-width:160px">2026-06-04</td><td style="min-width:160px">Amgen, Inc.</td><td style="min-width:160px">nationwide</td><td style="min-width:160px">Class II</td><td style="min-width:160px">FDA</td><td style="min-width:160px">Presence of foreign substance and CGMP deviations</td><td style="min-width:160px">Corlanor (ivabradine) and Sensipar (cinacalcet) medications</td><td style="min-width:160px">Drug</td><td style="min-width:160px">944,077</td></tr><tr><td style="min-width:40px">5</td><td style="min-width:280px">Oribe Serene Scalp Densifying Shampoo Recalled Due to Bacterial Contamination</td><td style="min-width:160px">2026-06-09</td><td style="min-width:160px">Kao USA Inc.</td><td style="min-width:160px">Alaska, Alabama, Arkansas, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia, Vermont, Wisconsin, West Virginia, District of Columbia, and Canada</td><td style="min-width:160px">Class II</td><td style="min-width:160px">FDA</td><td style="min-width:160px">Microbial contamination due to presence of Pluralibacter gergoviae</td><td style="min-width:160px">Oribae Serene Scalp Densifying Shampoo</td><td style="min-width:160px">Consumer Product</td><td style="min-width:160px">828</td></tr><tr class="catchall-blurred"><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td></tr><tr class="catchall-blurred"><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td></tr><tr class="catchall-blurred"><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td><td>████████████</td></tr></tbody></table>
<h3>What is the difference between this and the FDA's own recall Tracker?</h3><p>The FDA recall Tracker is comprehensive but presented in formats that are difficult to query programmatically and updated with delays. CatchAll structures confirmed recalls as events with enriched fields for product category, risk class, and recalling company.</p><h3>Are voluntary and mandatory recalls both included?</h3><p>Yes. Company-initiated voluntary recalls and FDA-mandated recalls are both included and distinguished by recall classification.</p><h3>Does the dataset cover recalls outside the US?</h3><p>The primary focus is US FDA and CPSC recalls. International recall data (Health Canada, EFSA) is not included in this edition.</p><h3>What is the refresh rate of this dataset?</h3><p>We rerun this dataset once a month. You can create your own dataset that updates as frequently as every one hour on <a href="https://platform.newscatcherapi.com/catchall">platform.newscatcherapi.com/catchall</a></p>