Par Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter

FDA Drug recall issued Sep 18, 2026.

ROCHESTER, MI– September 18, 2026 –Par Health is voluntarily recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection 400 mcg/100 mL (4 mcg/mL) to the hospital level. The product is being recalled due to the presence of particulate matter identified as cellulose or stopper materia

Check the lot code, best-by date, and package size on the agency notice before you throw anything out — most recalls cover only a few production runs, not the whole brand.

Do not open or taste a recalled food to judge it. Contamination like listeria, salmonella, or undeclared allergens has no smell or taste.

Wash anything the product touched — shelves, cutting boards, containers — with hot soapy water, then sanitize.

Keep the receipt or a photo of the label. Nearly every food recall includes a full refund with no receipt required, but a photo speeds it up.

If you or a family member got sick, call your doctor first, then report it to the agency using the link on the notice. Illness reports are how the recall gets widened.

Sourced from FDA and USDA public recall feeds. Notices are federal government works; we summarize dates and link to the official announcement.

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