CLASS I Drug recall · Reported 1 Jun 2016 · FDA Enforcement Report
Night Man recalled by R Thomas Marketing
R Thomas Marketing is recalling Night Man, distributed nationwide in the US. The recall was initiated on 9 Jan 2016 and the FDA has classified it as Class I.
Check your package
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-0903-2016
- FDA event ID
- 73018
- Recalling firm
- R Thomas Marketing, Bronx, NY
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 9 Jan 2016
- FDA classified
- 26 May 2016
- Reported
- 1 Jun 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Packaging Defects
Timeline
| 9 Jan 2016 | Recall initiated by company | |
| 26 May 2016 | Classified by FDA | +138 days |
| 1 Jun 2016 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed Without An Approved NDA/ANDA
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
Night Man, packaged in SMALL BOX (6 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Where it was distributed
Nationwide via Internet sales
Stores named: Online Retailers
Questions about this recall
Is Night Man recalled?
Yes. R Thomas Marketing recalled Night Man on 9 Jan 2016. The recall is Class I and its status is Terminated. Recall number D-0903-2016.
Why was it recalled?
Marketed Without An Approved NDA/ANDA
Which lots are affected?
all lots
Where was it sold?
Nationwide via Internet sales
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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.
More recalls from R Thomas Marketing
All 24| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Hard Ten Days recalled by R Thomas Marketing | R Thomas Marketing | Packaging Defects | Nationwide |
| Drug | CLASS I | Bull's Genital recalled by R Thomas Marketing | R Thomas Marketing | Packaging Defects | Nationwide |
| Drug | CLASS I | African Black Ant recalled by R Thomas Marketing | R Thomas Marketing | Packaging Defects | Nationwide |
| Drug | CLASS I | Super Hard recalled by R Thomas Marketing | R Thomas Marketing | Packaging Defects | Nationwide |
| Drug | CLASS I | Bigger Longer More Time More Sperms recalled by R Thomas Marketing | R Thomas Marketing | Packaging Defects | Nationwide |