The Recall Desk
ModerateFDA (Drugs)·D-1418-2014·Announced 2014-07-09

MD Custom Rx Recalls HCG Drops Due to Incorrect Solvent

MD Custom Rx is recalling HCG drops compounded with an incorrect solvent. The recall is limited to Wisconsin.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, which typically involves a temporary or medically reversible adverse health consequence. The source text does not report any specific illnesses or injuries, and the hazard is an incorrect excipient rather than a high-risk pathogen or structural defect.

Plain-English summary

Brookfield Prescription Center Inc. dba MD Custom Rx is recalling HCG (Human Chorionic Gonadotropin) 125 units/0.1 mL drops. The recall involves 5 mL bottles of the prescription-only medication.

The recall was initiated because specific drug products were compounded with an incorrect solvent. This is classified as an FDA Class II recall.

The affected products were distributed only in Wisconsin. Consumers should stop using the recalled products and contact their healthcare provider or pharmacist for further instructions.

The recalled product

Product
HCG (Human Chorionic Gonadotropin) 125 units/ 0.1 mL drop, 5 mL bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045
Manufacturer
Brookfield Prescription Center Inc. dba MD Custom Rx
Category
Drug — Compounded Prescription
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • Lot # / Beyond Use Date: 05192014@15 / BUD 07/18/14
  • 04142014@39 / BUD 6-13-14
  • 04182014@4 / BUD 6-17-14
  • 04162014@12 / BUD 06/15/14
  • 05092014@34 / BUD 07/08/14
  • 04162014@35 / BUD 06/15/14
  • 05232014@33 / BUD 07/22/14
  • 05022014@36 / BUD 7/1/14
  • 04292014@13 / BUD 06/28/14
  • 04282014@43 / BUD 06/27/14
  • 05212014@5 / BUD 07/20/14
  • 04292014@13 / BUD 06/28/14
  • 05062014@42 / BUD 07/05/14
  • 05022014@36 / BUD 07/01/14
  • 05062014@45 / BUD 07/05/14
  • 05082014@2 / BUD 07/07/14
  • 05152014@36 / BUD 7/14/14
  • 05132014@37 / BUD 07/12/14
  • 05082014@2 / BUD 07/07/14
  • 05132014@38 / BUD 07/12/14

Distribution

Distributed in 1 state:

Part of a larger recall action

This product is one of 6 recalled by Brookfield Prescription Center Inc. dba MD Custom Rx under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 6 products in this recall →

Related recalls

Same manufacturer · Brookfield Prescription Center Inc. dba MD Custom Rx

See all →

Same hazard · incorrect excipient

See all →