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Class II: temporary or reversible health riskTerminated

Vital Care Compounder Brilliant Blue G BBG Recall

Brilliant Blue G BBG, 0

Vital Care Compounder · Hattiesburg, MS

Risk level
Class II
Reported by FDA
Jul 6, 2016
Recall ID
D-1055-2016
Check your lot numberHow we source this data

Summary

Vital Care Compounder recalled Brilliant Blue G BBG starting Jun 10, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1055-2016 on Jul 6, 2016. Reason: Lack of Assurance of Sterility: Aluminum crimps do not fully seal the rubber stopper to the vials. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: Aluminum crimps do not fully seal the rubber stopper to the vials.

Product description

Brilliant Blue G BBG, 0.025%, Sterile Injection, 0.5 mL Single Dose Vial, Vital Care Compounder, Hattiesburg, MS

Lot numbers, UPCs & expiration codes

Lot#: 395575, Use by 07-27-2016

Where it was sold

MS

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-1055-2016
Classification
Class II
Status
Terminated
Recall initiated
Jun 10, 2015
FDA report date
Jul 6, 2016
Quantity
9 Vials
Recall type
Voluntary: Firm initiated
Recalling firm
Vital Care Compounder

Original FDA data

Every field from FDA enforcement report D-1055-2016, exactly as published.

Show all FDA fields
City
Hattiesburg
State
MS
Status
Terminated
Country
United States
Event ID
74539
Address
115 S 40th Ave
Code information
Lot#: 395575, Use by 07-27-2016
Postal code
39402-6600
Report date
Jul 6, 2016
Product type
Drugs
Recall number
D-1055-2016
Classification
Class II
Recalling firm
Vital Care Compounder
Product quantity
9 Vials
Termination date
Nov 17, 2016
Reason for recall
Lack of Assurance of Sterility: Aluminum crimps do not fully seal the rubber stopper to the vials.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Brilliant Blue G BBG, 0.025%, Sterile Injection, 0.5 mL Single Dose Vial, Vital Care Compounder, Hattiesburg, MS
Distribution pattern
MS
Recall initiation date
Jun 10, 2015
Initial firm notification
Telephone
Center classification date
Jun 28, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1055-2016, published Jul 6, 2016. 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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