CLASS I ONGOING Drug recall · Reported 21 Jun 2017 · FDA Enforcement Report
Human Chorionic Gonadotropin, 125 IU HCG, in syringe recalled
Complete Pharmacy and Medical Solutions is recalling Human Chorionic Gonadotropin, 125 IU HCG, in syringe, subcutaneous administration, distributed in Florida. The recall was initiated on 29 Dec 2015 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-0917-2017
- FDA event ID
- 76678
- Recalling firm
- Complete Pharmacy and Medical Solutions, Miami Lakes, FL
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 29 Dec 2015
- FDA classified
- 13 Jun 2017
- Reported
- 21 Jun 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Mold
Timeline
| 29 Dec 2015 | Recall initiated by company | |
| 13 Jun 2017 | Classified by FDA | +532 days |
| 21 Jun 2017 | Published 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
Non-sterility: presence of mold confirmed by outside laboratory at the 14 day culture.
Product as listed by the FDA
Human Chorionic Gonadotropin, 125 IU HCG, in 0.5 ml syringe, subcutaneous administration, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014
Where it was distributed
Distributed throughout Florida
Questions about this recall
Is Human Chorionic Gonadotropin, 125 IU HCG, in syringe, subcutaneous administration recalled?
Yes. Complete Pharmacy and Medical Solutions recalled Human Chorionic Gonadotropin, 125 IU HCG, in syringe, subcutaneous administration on 29 Dec 2015. The recall is Class I and its status is Ongoing. Recall number D-0917-2017.
Why was it recalled?
Non-sterility: presence of mold confirmed by outside laboratory at the 14 day culture.
Which lots are affected?
Lot # 2079ps5, Exp 02/01/2016
Where was it sold?
Distributed throughout 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 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.