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Press releases published on June 7, 2025

Keukenapparaatgids.nl Lanceert Onafhankelijke Gidsen Voor Koffiemachines en Keukenapparatuur
Keukenapparaatgids.nl biedt eerlijke reviews, koopgidsen en praktische tips voor koffieliefhebbers en keukenapparaatgebruikers. AMSTERDAM, NETHERLANDS, June 7, 2025 /EINPresswire.com/ -- Keukenapparaatgids.nl, een nieuwe Nederlandse website gericht op …

Couple Opens Unique '432Hz' Live Music Sanctuary on Spain's Costa del Sol for Summer Vibes and Son Awareness
British expats bring transformative live music experience to Málaga Province, combining wellness, community and authentic performances with 432Hz good vibes LONDON, LONDON, UNITED KINGDOM, June 7, 2025 /EINPresswire.com/ -- Carlos Unplugged, a new bar …

Sprouting Gear Inc. Founder Paul Pluss Announces Report on:
RAMONA, Calif., June 07, 2025 (GLOBE NEWSWIRE) -- The U.S. livestock industry, already grappling with rising feed costs and shrinking herd sizes, now faces a fast-approaching and under-recognized threat: the massive expansion of artificial intelligence (AI …

Church & Dwight Co., Inc. Issues Voluntary Nationwide Recall of Zicam® Cold Remedy Nasal Swabs, Zicam® Nasal AllClear Swabs, and Orajel™ Baby Teething Swabs Due to Microbial Contamination
COMPANY ANNOUNCEMENT When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read Announcement View Product Photos Summary …

August Egg Company Recalls Shell Eggs Because of Possible Health Risk
Summary Company Announcement Date: June 06, 2025 FDA Publish Date: June 06, 2025 Product Type: Food …

August Egg Company Recalls Shell Eggs Because of Possible Health Risk
Summary Company Announcement Date: June 06, 2025 FDA Publish Date: June 06, 2025 Product Type: Food …

Infusion Pump Correction: Baxter Updates Instructions for Use for Novum IQ Large Volume Pump due to Potential for Underinfusion
This recall involves updating instructions for using devices and does not involve removing them from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to …

Church & Dwight Co., Inc. Issues Voluntary Nationwide Recall of Zicam® Cold Remedy Nasal Swabs, Zicam® Nasal AllClear Swabs, and Orajel™ Baby Teething Swabs Due to Microbial Contamination
COMPANY ANNOUNCEMENT When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read Announcement View Product Photos Summary …