CLASS III Drug recall · Reported 15 Aug 2018 · FDA Enforcement Report

Testosterone 200 mg Pellet recalled by Right Value Drug Stores

Right Value Drug Stores is recalling Testosterone 200 mg Pellet, distributed nationwide in the US. The recall was initiated on 26 Jul 2018 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot #: 061918@08, Exp.11/28/2019
Quantity recalled4800 pellets

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-1047-2018
FDA event ID
80655
Recalling firm
Right Value Drug Stores, Hurst, TX
Classification
Class III
Status
Terminated
Recall initiated
26 Jul 2018
FDA classified
7 Aug 2018
Reported
15 Aug 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

26 Jul 2018Recall initiated by company
7 Aug 2018Classified by FDA+12 days
15 Aug 2018Published in enforcement report+8 days

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

Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date: Incorrect expiration date on label

Product as listed by the FDA

Testosterone 200 mg Pellet, Rx only, Carie Boyd's Prescription Shop 122 Grapevine Hwy., Hurst, TX 76054, 800-930-4361

Where it was distributed

Nationwide with the United States

Nationwide

Questions about this recall

Why was it recalled?

Labeling: Incorrect or Missing Lot and/or Exp Date: Incorrect expiration date on label

Which lots are affected?

Lot #: 061918@08, Exp.11/28/2019

Where was it sold?

Nationwide with the United States

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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