Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Mar 22, 2018 (9 years ago)

HCG 1000 units/mL

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.

Cause type: Sterility / contamination

A product that must be sterile could not be assured sterile, or was contaminated. A top reason for injectables, eye drops and IV products - loss of sterility assurance can lead to serious infections. All sterility / contamination recalls.

What was recalled

HCG 1000 units/mL, packaged in a) 2 mL and b) 6 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

Recalling firm
Partell Specialty Pharmacy
Origin
NV, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0639-2018 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Partell Specialty Pharmacy

All 2018 recalls
Class II · Moderate risk

Estradiol 55 mg

Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.

Terminated Sterility / contamination Partell Specialty Pharmacy D-0681-2018
Class II · Moderate risk

Estradiol 50 mg

Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.

Terminated Sterility / contamination Partell Specialty Pharmacy D-0680-2018
Class II · Moderate risk

Estradiol 40 mg

Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.

Terminated Sterility / contamination Partell Specialty Pharmacy D-0679-2018

Other sterility / contamination recalls from 2018

All sterility / contamination recalls