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Class II: temporary or reversible health riskTerminated

Olympia Compounding Pharmacy dba Olympia Pharmacy Testosterone Cypionate 200 mg/mL Recall

Testosterone Cypionate 200 mg/mL (in Grapeseed Oil), Packaged in a) 10 mL Multi-Dose vial

Olympia Compounding Pharmacy dba Olympia Pharmacy · Orlando, FL

Risk level
Class II
Reported by FDA
May 4, 2022
Recall ID
D-0823-2022
Check your lot numberHow we source this data

Summary

Olympia Compounding Pharmacy dba Olympia Pharmacy recalled Testosterone Cypionate 200 mg/mL starting Apr 4, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0823-2022 on May 4, 2022. Reason: CGMP Deviations: prior to October 1, 2021, environmental and personnel monitoring Out of Action Limit (OOAL) excursions were not being properly investigated. Status: Terminated.

Why it was recalled

CGMP Deviations: prior to October 1, 2021, environmental and personnel monitoring Out of Action Limit (OOAL) excursions were not being properly investigated

Product description

Testosterone Cypionate 200 mg/mL (in Grapeseed Oil), Packaged in a) 10 mL Multi-Dose vial, NDC 73198-0054-10; b) 5 mL Multi-Dose vial, NDC 73198-0054-05, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835.

Lot numbers, UPCs & expiration codes

Lots: a) D48027 BUD: 4/27/2022,E47017 BUD: 5/17/2022, F42007 BUD: 6/7/2022, F42107 BUD: 6/7/2022, F42207 BUD: 6/7/2022, F48009 BUD: 6/9/2022, F48109 BUD: 6/9/2022, H47003 BUD: 8/3/2022; b) F24024 BUD: 6/24/2022

Where it was sold

Distributed Nationwide in the USA

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-0823-2022
Classification
Class II
Status
Terminated
Recall initiated
Apr 4, 2022
FDA report date
May 4, 2022
Quantity
7161 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Olympia Compounding Pharmacy dba Olympia Pharmacy

Original FDA data

Every field from FDA enforcement report D-0823-2022, exactly as published.

Show all FDA fields
City
Orlando
State
FL
Status
Terminated
Country
United States
Event ID
89938
Address
6700 Conroy Rd Ste 155
Code information
Lots: a) D48027 BUD: 4/27/2022,E47017 BUD: 5/17/2022, F42007 BUD: 6/7/2022, F42107 BUD: 6/7/2022, F42207 BUD: 6/7/2022, F48009 BUD: 6/9/2022, F48109 BUD: 6/9/2022, H47003 BUD: 8/3/2022; b) F24024 BUD: 6/24/2022
Postal code
32835-3515
Report date
May 4, 2022
Product type
Drugs
Recall number
D-0823-2022
Classification
Class II
Recalling firm
Olympia Compounding Pharmacy dba Olympia Pharmacy
Product quantity
7161 vials
Termination date
Jun 17, 2024
Reason for recall
CGMP Deviations: prior to October 1, 2021, environmental and personnel monitoring Out of Action Limit (OOAL) excursions were not being properly investigated
Voluntary / mandated
Voluntary: Firm initiated
Product description
Testosterone Cypionate 200 mg/mL (in Grapeseed Oil), Packaged in a) 10 mL Multi-Dose vial, NDC 73198-0054-10; b) 5 mL Multi-Dose vial, NDC 73198-0054-05, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835.
Distribution pattern
Distributed Nationwide in the USA
Recall initiation date
Apr 4, 2022
Initial firm notification
Letter
Center classification date
Apr 27, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0823-2022, published May 4, 2022. View the source record (openFDA) · FDA enforcement reports

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

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