CLASS III Drug recall · Reported 16 Sep 2015 · FDA Enforcement Report

Cvs Sugar Free Black Cherry Cough Drops (menthol-cough Suppressant) recalled

Bestco is recalling Cvs Sugar Free Black Cherry Cough Drops (menthol-cough Suppressant), distributed nationwide in the US. The recall was initiated on 2 Jul 2015 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesa) Lot #: 50122U3, Expiry: 01/2017; Lot #: 50122U1, Expiry: 01/2017; and b) Lot #: 50122U2, Expiry: 01/2017.
Quantity recalleda) 149,856 Bags; b) 19,200 Bags.

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-1419-2015
FDA event ID
72069
Recalling firm
Bestco, Mooresville, NC
Classification
Class III
Status
Terminated
Recall initiated
2 Jul 2015
FDA classified
9 Sep 2015
Reported
16 Sep 2015
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Packaging Defects

Timeline

2 Jul 2015Recall initiated by company
9 Sep 2015Classified by FDA+69 days
16 Sep 2015Published in enforcement report+7 days

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

Reason for recall

Presence of Foreign Tablets/Capsules: Presence of comingled Sugar Free Honey Lemon cough drops.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT), Packaged in a) 25 Drop Bags (UPC: 050428 448526) and b) 36 drop bags (UPC: 050428 476581), Over the Counter. Distributed by: CVS Pharmacy, Inc., One CVS Drive Woonsocket, RI 02895.

Where it was distributed

U.S. Nationwide

Nationwide

Stores named: CVS

Questions about this recall

Why was it recalled?

Presence of Foreign Tablets/Capsules: Presence of comingled Sugar Free Honey Lemon cough drops.

Which lots are affected?

a) Lot #: 50122U3, Expiry: 01/2017; Lot #: 50122U1, Expiry: 01/2017; and b) Lot #: 50122U2, Expiry: 01/2017.

Where was it sold?

U.S. Nationwide

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 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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