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Class II: temporary or reversible health riskTerminated

Zions RX Formulations Services LLC dba RX Formuations Serv. Bupivacaine 3% Recall

Bupivacaine 3%, 300 mL units, Not for Dispensing, For Hospital Administration Only, Rx…

Zions RX Formulations Services LLC dba RX Formuations Serv. · Mesa, AZ

Risk level
Class II
Reported by FDA
Apr 16, 2014
Recall ID
D-1218-2014
Check your lot numberHow we source this data

Summary

Zions RX Formulations Services LLC dba RX Formuations Serv. recalled Bupivacaine 3% starting Dec 12, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1218-2014 on Apr 16, 2014. Reason: Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices observed at the firm. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices observed at the firm.

Product description

Bupivacaine 3%, 300 mL units, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ 85205

Lot numbers, UPCs & expiration codes

Lot #: 117456@3 Expiration Date: 12/12/2013 Lot #: 117907@3 Expiration Date: 12/19/2013 Lot #: 118297@8 Expiration Date: 12/25/2013

Where it was sold

AZ

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-1218-2014
Classification
Class II
Status
Terminated
Recall initiated
Dec 12, 2013
FDA report date
Apr 16, 2014
Quantity
60 units
Recall type
Voluntary: Firm initiated
Recalling firm
Zions RX Formulations Services LLC dba RX Formuations Serv.

Original FDA data

Every field from FDA enforcement report D-1218-2014, exactly as published.

Show all FDA fields
City
Mesa
State
AZ
Status
Terminated
Country
United States
Event ID
67080
Address
5949 E University Dr
Code information
Lot #: 117456@3 Expiration Date: 12/12/2013 Lot #: 117907@3 Expiration Date: 12/19/2013 Lot #: 118297@8 Expiration Date: 12/25/2013
Postal code
85205-7435
Report date
Apr 16, 2014
Product type
Drugs
Recall number
D-1218-2014
Classification
Class II
Recalling firm
Zions RX Formulations Services LLC dba RX Formuations Serv.
Product quantity
60 units
Termination date
May 1, 2014
Reason for recall
Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices observed at the firm.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Bupivacaine 3%, 300 mL units, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ 85205
Distribution pattern
AZ
Recall initiation date
Dec 12, 2013
Initial firm notification
E-Mail
Center classification date
Apr 7, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1218-2014, published Apr 16, 2014. 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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