CLASS II Drug recall · Reported 1 Apr 2020 · FDA Enforcement Report

Buprenorphine Black Cherry 2 mg Troche, supplied recalled

Matthew 7:25 is recalling Buprenorphine Black Cherry 2 mg Troche, supplied in plastic troche molds with cardboard, distributed in Florida. The recall was initiated on 10 Mar 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 191217A Exp. 06/14/2020
Quantity recalled89 troches

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1054-2020
FDA event ID
85207
Recalling firm
Matthew 7:25, Jacksonville, FL
Classification
Class II
Status
Terminated
Recall initiated
10 Mar 2020
FDA classified
23 Mar 2020
Reported
1 Apr 2020
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Foreign Material

Timeline

10 Mar 2020Recall initiated by company
23 Mar 2020Classified by FDA+13 days
1 Apr 2020Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Subpotent Drug

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Buprenorphine Black Cherry 2 mg Troche, supplied in plastic troche molds with cardboard outer sleeve, Thrive Pharmacy 2863 St Johns Bluff RD. South # 135 Jacksonville, Florida

Where it was distributed

Florida

Florida

Questions about this recall

Is Buprenorphine Black Cherry 2 mg Troche, supplied in plastic troche molds with cardboard recalled?

Yes. Matthew 7:25 recalled Buprenorphine Black Cherry 2 mg Troche, supplied in plastic troche molds with cardboard on 10 Mar 2020. The recall is Class II and its status is Terminated. Recall number D-1054-2020.

Why was it recalled?

Subpotent Drug

Which lots are affected?

Lot: 191217A Exp. 06/14/2020

Where was it sold?

Florida

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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