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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

Detected September 21, 2026 · in Food & Beverage Manufacturing (FDA/FSMA/USDA)

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 — recall update affecting Food & Beverage Manufacturing (FDA/FSMA/USDA).

Aforeworn detected this change in the Food & Beverage Manufacturing (FDA/FSMA/USDA) space on September 21, 2026 and published this briefing so affected operators are forewarned rather than caught off guard. It is rated Low urgency. Food & Beverage Manufacturing (FDA/FSMA/USDA) (food manufacturers, beverage makers, co-packers / private label, ingredient suppliers) should confirm how it applies to their specific situation before acting. Aforeworn monitors Food & Beverage Manufacturing (FDA/FSMA/USDA) continuously and turns every detected change into a plain-English briefing like this one, so you always know first. Forewarned is forearmed.

What changed

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

Who it affects

Food & Beverage Manufacturing (FDA/FSMA/USDA) (food manufacturers, beverage makers, co-packers / private label, ingredient suppliers)

What you must do

Read the update and assess whether your current setup needs to change.

Deadline

No fixed deadline was published, but changes like this are often enforced quickly — act promptly.

Source: http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-health-issues-voluntary-nationwide-recall-two-lots-dexmedetomidine-hcl-09-sodium-chloride

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