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Tirzepatide/Niacinamide 2mL vial Inj 20mg/2mg/mL, RX Only, Houston RX LLC Recall 2026

Houston Rx LLCIssued September 25, 2026Updated Reviewed by the Recall Watch editorial team

Houston Rx LLC Tirzepatide/Niacinamide 2mL vial (40 MG per Vial) Inj 20mg/2mg/mL, RX Only, Houston RX LLC, 15430 Vantage Parkway E STE 220, Houston, TX 77032. — recalled per FDA on 9/25/2026. Reason: Lack of assurance of sterility..

Agency
FDA
Issued
Sep 25, 2026
Brand
Houston Rx LLC
Distribution
1 states
Lots affected
2
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 September 25, 2026 · Last synced Oct 26, 2026

What's recalled

Tirzepatide/Niacinamide 2mL vial (40 MG per Vial) Inj 20mg/2mg/mL, RX Only, Houston RX LLC, 15430 Vantage Parkway E STE 220, Houston, TX 77032.

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Why it was recalled

Lack of assurance of sterility.

Affected products & lot numbers
2 lots called out

Affected Lot Numbers

Check your product label — do not use if your lot number appears below.

Lot Number
Lot# TZN-080326-20/2-2
Beyond Use Date: 12/01/2026.
Where was it sold
1 state

Nationwide in the USA.

nationwide
Official noticefda.gov
More recalls like this
5 related — by brand, contaminant, and category

Frequently asked questions

Is the Houston Rx LLC recall still active?

Yes, this recall is currently active as of September 25, 2026. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: Lot# TZN-080326-20/2-2, Beyond Use Date: 12/01/2026.. Check the label on your product.

What should I do if I have the recalled Houston Rx LLC?

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