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Class II: temporary or reversible health riskTerminated

Qualgen Estradiol 6 mg pellet 99 Recall

Estradiol 6 mg pellet 99

Qualgen · Edmond, OK

Risk level
Class II
Reported by FDA
Jun 14, 2017
Recall ID
D-0896-2017
Check your lot numberHow we source this data

Summary

Qualgen recalled Estradiol 6 mg pellet 99 starting Apr 19, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0896-2017 on Jun 14, 2017. Reason: CGMP deviations- Lack of Quality Assurance. Status: Terminated.

Why it was recalled

CGMP deviations- Lack of Quality Assurance

Product description

Estradiol 6 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by; Qualgen 14844 Bristol Park Blvd. Edmond, OK 73013 NDC: 69761-006-01.

Lot numbers, UPCs & expiration codes

Lot# C046; Exp. 03/15/18 Lot# C025; Exp. 08/23/17 Lot# B159; Exp. 12/28/17 Lot# B121; Exp. 10/10/17 Lot# B118; Exp. 10/17/17 Lot# B086; Exp. 08/29/17 Lot# B068; Exp. 07/11/17 Lot# B053; Exp. 06/14/17 Lot# B034; Exp. 04/26/17

Where it was sold

Nationwide.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0896-2017
Classification
Class II
Status
Terminated
Recall initiated
Apr 19, 2017
FDA report date
Jun 14, 2017
Quantity
4,815 pellets.
Recall type
Voluntary: Firm initiated
Recalling firm
Qualgen

Original FDA data

Every field from FDA enforcement report D-0896-2017, exactly as published.

Show all FDA fields
City
Edmond
State
OK
Status
Terminated
Country
United States
Event ID
77064
Address
14844 Bristol Park Blvd
Code information
Lot# C046; Exp. 03/15/18 Lot# C025; Exp. 08/23/17 Lot# B159; Exp. 12/28/17 Lot# B121; Exp. 10/10/17 Lot# B118; Exp. 10/17/17 Lot# B086; Exp. 08/29/17 Lot# B068; Exp. 07/11/17 Lot# B053; Exp. 06/14/17 Lot# B034; Exp. 04/26/17
Postal code
73013-1891
Report date
Jun 14, 2017
Product type
Drugs
Recall number
D-0896-2017
Classification
Class II
Recalling firm
Qualgen
Product quantity
4,815 pellets.
Termination date
Sep 24, 2021
Reason for recall
CGMP deviations- Lack of Quality Assurance
Voluntary / mandated
Voluntary: Firm initiated
Product description
Estradiol 6 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by; Qualgen 14844 Bristol Park Blvd. Edmond, OK 73013 NDC: 69761-006-01.
Distribution pattern
Nationwide.
Recall initiation date
Apr 19, 2017
Initial firm notification
Letter
Center classification date
Jun 7, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0896-2017, published Jun 14, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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