@anxinapp: FDA Recall Alert: Par Health has recalled 22 lots of the hospital blood thinner Argatroban after particles — possibly including stainless steel — turned up in vials. Par Health USA (Rochester, MI) issued a nationwide, hospital-level recall of Argatroban Injection (250 mg/2.5 mL) after particulate matter — cellulose, polystyrene, stopper material, and possibly stainless steel — was found in certain vials. If infused, it carries a reasonable probability of serious harm: pulmonary embolism, blocked blood vessels, or vein inflammation. The affected lots shipped nationwide to hospitals and wholesalers between December 2024 and May 2026. No adverse events have been reported. This one's hospital-administered, not something you'd have at home — but it's a reminder that even hospital supply chains aren't immune to the gap Anxin exists to close. Anxin surfaces every piece of a recall — in your pantry or down the hospital supply chain. Download Anxin — free at pieceofmind.fyi

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