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Biospectra Tris/Tromethamine, USP, GMP, API Grade, Manufactured at 100 Recall 2026

BioSpectra, Inc.Issued July 29, 2026Updated Reviewed by the Recall Watch editorial team

BioSpectra, Inc. Biospectra Tris/Tromethamine, USP, GMP, API Grade, Manufactured at 100 Majestic Way, Bangor, PA 18013, NDC 64173-101-25 — recalled per FDA on 7/29/2026. Reason: Failed stability specifications.

Agency
FDA
Issued
Jul 29, 2026
Brand
BioSpectra, Inc.
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 July 29, 2026 · Last synced Oct 21, 2026

What's recalled

Biospectra Tris/Tromethamine, USP, GMP, API Grade, Manufactured at 100 Majestic Way, Bangor, PA 18013, NDC 64173-101-25

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Why it was recalled

Failed stability specifications

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#: TRIS -E04-0226-0016
Exp 2/29/28
Where was it sold
1 state

CA

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

Frequently asked questions

Is the BioSpectra, Inc. recall still active?

Yes, this recall is currently active as of July 29, 2026. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: Lot#: TRIS -E04-0226-0016, Exp 2/29/28. Check the label on your product.

What should I do if I have the recalled BioSpectra, Inc.?

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