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FDAClass II

Biospectra Tris/Tromethamine, USP, GMP, API Grade, Manufactured at 100 Majestic Way, Bang… Recalled: Failed stability specifications

Biospectra Tris/Tromethamine, USP, GMP, API Grade,… was recalled on July 29, 2026 in cooperation with the U.S. Food and Drug Administration because failed stability specifications.

Is my unit affected?

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

Model, lot & date codes to check

Lot#: TRIS -E04-0226-0016; Exp 2/29/28

Units affected: 200 kg

Where it was sold: CA

Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.

What's the hazard?

Failed stability specifications

Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.

Your remedy & how to claim it

Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.

Contact: Recalling firm: BioSpectra, Inc.

Not sure what you're entitled to? Read our guide: what to do if your product is recalled.

Official recall notice

Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.

View official notice →

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