FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

Walgreens Infusion Services Ceftazidime various strength in normal Recall

Ceftazidime various strength in normal saline bags

Walgreens Infusion Services · Houston, TX

Risk level
Class II
Reported by FDA
Jan 28, 2015
Recall ID
D-0345-2015
Check your lot numberHow we source this data

Summary

Walgreens Infusion Services recalled Ceftazidime various strength in normal starting Dec 26, 2014. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0345-2015 on Jan 28, 2015. Reason: Lack of sterility assurance. Status: Terminated.

Why it was recalled

Lack of sterility assurance.

Product description

Ceftazidime various strength in normal saline bags

Lot numbers, UPCs & expiration codes

All products within expiry.

Where it was sold

Texas, Florida, Virginia, Georgia, Louisiana, Mississippi

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-0345-2015
Classification
Class II
Status
Terminated
Recall initiated
Dec 26, 2014
FDA report date
Jan 28, 2015
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
Walgreens Infusion Services

Original FDA data

Every field from FDA enforcement report D-0345-2015, exactly as published.

Show all FDA fields
City
Houston
State
TX
Status
Terminated
Country
United States
Event ID
70118
Address
9030 Kirby Dr
Code information
All products within expiry.
Postal code
77054-2504
Report date
Jan 28, 2015
Product type
Drugs
Recall number
D-0345-2015
Classification
Class II
Recalling firm
Walgreens Infusion Services
Termination date
Jul 24, 2015
Reason for recall
Lack of sterility assurance.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Ceftazidime various strength in normal saline bags
Distribution pattern
Texas, Florida, Virginia, Georgia, Louisiana, Mississippi
Recall initiation date
Dec 26, 2014
Initial firm notification
Letter
Center classification date
Jan 16, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0345-2015, published Jan 28, 2015. 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.

How we source and update recall data · Report incorrect information

Other recent drug recalls