Complete Pharmacy and Medical Solutions, LLC. recalls HUMAN CHORIONIC GONADOTROPIN 1,250 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection.
Complete Pharmacy recalls HUMAN CHORIONIC GONADOTROPIN 1,250 IU vials due to lack of potency testing. Affected lots were manufactured in Miami Lakes, FL.
Lower-risk recall
CGMP deviations: Lack of potency testing.
Contact the company & request your remedy
What happened, in plain English
Complete Pharmacy is recalling HUMAN CHORIONIC GONADOTROPIN 1,250 IU vials that contain Mannitol 9% and Sodium Phosphate 2% because they failed potency testing. This means the product may not work as intended for medical use. Read more at govinfonow.com/recall/36659-complete-pharmacy-recalls-cgm-1250-iu-vials-lack-of-potency.
Source Summary by GovInfoNow · govinfonow.com/recall/36659-complete-pharmacy-recalls-cgm-1250-iu-vials-lack-of-potency · Updated October 4, 2026 · FDA enforcement record: FDA #D-0237-2021
Cite this page
“Complete Pharmacy recalls CGM 1250 IU vials: Lack of potency testing.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36659-complete-pharmacy-recalls-cgm-1250-iu-vials-lack-of-potency. Based on FDA recall #D-0237-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0237-2021%22&limit=1).
Why it’s dangerous
The product was made without proper potency testing, which means it might not have the correct amount of active ingredient. This could lead to ineffective treatment if used medically.
Who’s affected
Healthcare providers and patients using this specific hormone product for medical treatments. Those with the lot number 40548 are most at risk.
How to tell if you have this one
Check for the lot number 40548 on the vial label. The product contains Mannitol 9% and Sodium Phosphate 2% in water for injection. It was manufactured in Miami Lakes, FL.
- Brand
Complete Pharmacy- Category
Drug
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Distributed Nationwide in the USA
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0234-2021 | HUMAN CHORIONIC GONADOTROPIN 11,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035; Lot #: 40568 Use By Date: 01/30/2021 | 1182 vials |
| D-0235-2021 | HUMAN CHORIONIC GONADOTROPIN 6,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035; Lot# 40604 Use By date, 01/30/2021 | 2418 vials |
| D-0236-2021 | HUMAN CHORIONIC GONADOTROPIN 5,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035; Lot #: 40570 Use By Date 01/30/2021 | 1144 vials |
| D-0237-2021 | HUMAN CHORIONIC GONADOTROPIN 1,250 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035; Lot #: 40548, Use By Date, 01/30/2021. | 2400 vials |
What to do — step by step
Check Vial Label
Look for the lot number 40548 on the vial label to confirm if it is affected.
Questions people ask
Why is this product being recalled?
The product failed potency testing, meaning it may not have the correct amount of active ingredient for medical use.
What should I do if I have this product?
Check the vial label for the lot number 40548. If it matches, stop using it and contact Complete Pharmacy for guidance.
Is there a deadline to act?
The official recall notice does not specify a deadline for action.
Contact Complete Pharmacy
We’ve drafted a message you can send Complete Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0237-2021 — Complete Pharmacy Complete Pharmacy Hello, I own a Complete Pharmacy that is covered by recall D-0237-2021 from Complete Pharmacy. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0237-2021 (November 20, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0237-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.