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Verified · FDAClass II — Possible RiskMedications

Par Pharmaceutical Par Health Issues Voluntary Nationwide Two Lots Recall 2026

Par PharmaceuticalIssued October 8, 2026Updated Reviewed by the Recall Watch editorial team

Par Pharmaceutical Par Health Issues Voluntary Nationwide Recall of Two Lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) Due to the Presence of Particulate Matter — recalled per FDA on 10/8/2026. Reason: Presence of particulate matter identified as cellulose.

Agency
FDA
Issued
Oct 8, 2026
Brand
Par Pharmaceutical
States affected
1
What to do right now

Steps to take for this recall

  1. Stop using it

    Take it out of rotation. Don't consume, wear, or operate.

  2. Verify the match

    Compare lot numbers, UPCs, and dates against your product.

  3. Return or dispose

    Follow the manufacturer's instructions to refund or safely dispose.

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Verified summary of the official U.S. Food and Drug Administration notice · Issued October 8, 2026 · Last synced Oct 22, 2026

What's recalled

Company: Par Health Brand(s): Par Pharmaceutical Brevital Sodium 500 mg/vial for Injection

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Why it was recalled

Presence of particulate matter identified as cellulose

Where was it sold
1 state
nationwide
Official noticefda.gov
More recalls like this
4 related — by brand, contaminant, and category

Frequently asked questions

Is the Par Pharmaceutical recall still active?

Yes, this recall is currently active as of October 8, 2026. Do not use or consume the affected product.

How do I know if my Par Pharmaceutical is affected?

All units of Par Pharmaceutical matching the description above are affected.

What should I do if I have the recalled Par Pharmaceutical?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.