CLASS II Drug recall · Reported 22 Apr 2020 · FDA Enforcement Report
Progesterone/Versa Base 20 mg (2%) Cream 30 gm tube, Rx recalled
The Medicine Shoppe Pharmacy is recalling Progesterone/Versa Base 20 mg (2%) Cream 30 gm tube, Rx, The Medicine Shoppe Pharmacy, distributed in Florida. The recall was initiated on 6 Apr 2020 and the FDA has classified it as Class II.
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-1190-2020
- FDA event ID
- 85404
- Recalling firm
- The Medicine Shoppe Pharmacy, Port Charlotte, FL
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Apr 2020
- FDA classified
- 10 Apr 2020
- Reported
- 22 Apr 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Drug class
- Hormones & Birth Control
Timeline
| 6 Apr 2020 | Recall initiated by company | |
| 10 Apr 2020 | Classified by FDA | +4 days |
| 22 Apr 2020 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of Processing Control
Product as listed by the FDA
Progesterone/Versa Base 20 mg (2%) Cream 30 gm tube, Rx, The Medicine Shoppe Pharmacy, Port Charlotte, FL
Where it was distributed
Florida
Questions about this recall
Why was it recalled?
Lack of Processing Control
Which lots are affected?
Lot: 45104 Discard by: 8/18/2020
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 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.
Other products in this recall event
53 other products · FDA event 85404This product is part of a recall event; the main page for the event is Bi-Est (1 /Progesterone/Testosterone 2.5/150/1.5 mg/mL recalled.
More recalls from The Medicine Shoppe Pharmacy
All 55| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Clobetasol Mouth Rinse 0.05% Solution, Rx recalled | The Medicine Shoppe Pharmacy | Other | FL |
| Drug | CLASS II | Bi-Est (1 /Progesterone/Testosterone 2.0 mg/40 mg/1.0 mg/mL recalled | The Medicine Shoppe Pharmacy | Other | FL |
| Drug | CLASS II | Naltrexone (Loxoral) recalled by The Medicine Shoppe Pharmacy | The Medicine Shoppe Pharmacy | Other | FL |
| Drug | CLASS II | Bi-Est (1 Progest/Test 0.5 mg/40 mg/10.5 mg/mL Cream 30 gm recalled | The Medicine Shoppe Pharmacy | Other | FL |
| Drug | CLASS II | Bi-Est (8 /Progesterone 2/100 mg/mL capsule 90 caps, Rx recalled | The Medicine Shoppe Pharmacy | Other | FL |
Other Progesterone recalls
All 29| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Progesterone Injection USP, 500mg per (50mg/mL) Multiple Dose Vial recalledProgesterone | Eugia US | Particulate Matter | Nationwide |
| Drug | CLASS II | Progesterone Injection, USP, 500 mg per (50mg/mL) Multiple-Dose Vial recalledProgesterone | Eugia US | Particulate Matter | Nationwide |
| Drug | CLASS II | Progesterone 200 mg, Compounded, Rx recalled by Coast Quality Pharmacy | Coast Quality Pharmacy | Foreign Material | Nationwide |
| Drug | CLASS II | Progesterone 100mg/ML Inj # Ethyl Oleate Injectable recalled | Vita Pharmacy | Sterility | DC, PR |
| Drug | CLASS II | Progesterone 100mg/ML Mdv Oil Injection recalled | First Royal Care Co. LLC | Sterility | 7 states |