Skip to main content
Skip to recall details
Verified · FDAClass II — Possible RiskMedications

Par Health Issues Voluntary Nationwide Argatroban Injection Recall 2026

Par Health and Endo USAIssued October 13, 2026Updated Reviewed by the Recall Watch editorial team

Par Health and Endo USA Par Health Issues Voluntary Nationwide Recall of Argatroban Injection Due to the Presence of Particulate Matter — recalled per FDA on 10/13/2026. Reason: Presence of particulate matter, identified as cellulose, polystyrene, polyethylene terephthalate, stopper material, and possibly stainless steel.

Agency
FDA
Issued
Oct 13, 2026
Brand
Par Health and Endo USA
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.

Free case review

Were you or someone in your household prescribed this medication?

  • Free
  • No obligation
  • Licensed attorneys
Attorney advertising.Details

Recall Watch is not a law firm and does not provide legal or medical advice. Free case reviews are provided by independent licensed attorneys; Recall Watch may receive a referral fee. Prior results do not guarantee a similar outcome. Submitting this form does not create an attorney-client relationship. See our terms and privacy policy.

Verified summary of the official U.S. Food and Drug Administration notice · Issued October 13, 2026 · Last synced Oct 22, 2026

What's recalled

Company: Par Health USA, LLC Brand(s): Par Health and Endo USA Argatroban Injection 250 mg/2.5 mL (100 mg/mL)

Available at AmazonAd
White first-aid box with bandages

Restock your medicine cabinet

First-aid kits, thermometers and OTC basics, searched on Amazon.

Shop at Amazon.com

Need it delivered? Start a free Amazon Prime trial.

Why it was recalled

Presence of particulate matter, identified as cellulose, polystyrene, polyethylene terephthalate, stopper material, and possibly stainless steel

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 Health and Endo USA recall still active?

Yes, this recall is currently active as of October 13, 2026. Do not use or consume the affected product.

How do I know if my Par Health and Endo USA is affected?

All units of Par Health and Endo USA matching the description above are affected.

What should I do if I have the recalled Par Health and Endo USA?

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