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Class II: temporary or reversible health riskTerminated

Key Pharmacy and Compounding Center Pge1/Procaine 5ml Mdv 20mcg/Ml/0 Recall

PGE1/PROCAINE 5ML MDV 20MCG/ML/0

Key Pharmacy and Compounding Center · Federal Way, WA

Risk level
Class II
Reported by FDA
May 24, 2017
Recall ID
D-0756-2017
Check your lot numberHow we source this data

Summary

Key Pharmacy and Compounding Center recalled Pge1/Procaine 5ml Mdv 20mcg/Ml/0 starting Apr 18, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0756-2017 on May 24, 2017. Reason: Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Product description

PGE1/PROCAINE 5ML MDV 20MCG/ML/0.1% INJ, Injection, 20mcg/ml 0.1%, Rx only, 5 mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy

Lot numbers, UPCs & expiration codes

Lot # t12-12-2016@92, Exp 5/22/2017; t02-14-2017@103, Exp 8/2/2017

Where it was sold

Distributed nationwide in U.S.A., Australia and Canada.

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-0756-2017
Classification
Class II
Status
Terminated
Recall initiated
Apr 18, 2017
FDA report date
May 24, 2017
Quantity
3 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Key Pharmacy and Compounding Center

Original FDA data

Every field from FDA enforcement report D-0756-2017, exactly as published.

Show all FDA fields
City
Federal Way
State
WA
Status
Terminated
Country
United States
Event ID
76912
Address
530 S 336th St
Code information
Lot # t12-12-2016@92, Exp 5/22/2017; t02-14-2017@103, Exp 8/2/2017
Postal code
98003-6383
Report date
May 24, 2017
Product type
Drugs
Recall number
D-0756-2017
Classification
Class II
Recalling firm
Key Pharmacy and Compounding Center
Product quantity
3 vials
Termination date
Aug 29, 2017
Reason for recall
Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.
Voluntary / mandated
Voluntary: Firm initiated
Product description
PGE1/PROCAINE 5ML MDV 20MCG/ML/0.1% INJ, Injection, 20mcg/ml 0.1%, Rx only, 5 mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
Distribution pattern
Distributed nationwide in U.S.A., Australia and Canada.
Recall initiation date
Apr 18, 2017
Initial firm notification
Letter
Center classification date
May 17, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0756-2017, published May 24, 2017. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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