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Class II: temporary or reversible health riskTerminated

Baxter Healthcare Lidocaine Hydrochloride and 5% Dextrose Recall

Lidocaine Hydrochloride and 5% Dextrose Injection, USP, 2g VIAFLEX Plus Plastic Contain…

Baxter Healthcare Corp. · Deerfield, IL

Risk level
Class II
Reported by FDA
Jul 10, 2013
Recall ID
D-627-2013
Check your lot numberHow we source this data

Summary

Baxter Healthcare recalled Lidocaine Hydrochloride and 5% Dextrose starting May 21, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-627-2013 on Jul 10, 2013. Reason: Lack of Assurance of Sterilty: Specific lot numbers of these products have been identified for potential administration port leakage. The potential for leakage is the result of a manufacturing issue which occurred during the sealing of the closure assembly at the administration port. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterilty: Specific lot numbers of these products have been identified for potential administration port leakage. The potential for leakage is the result of a manufacturing issue which occurred during the sealing of the closure assembly at the administration port.

Product description

Lidocaine Hydrochloride and 5% Dextrose Injection, USP, 2g VIAFLEX Plus Plastic Container, 500mL, Rx Only, Baxter, Deerfield, IL 60015

Lot numbers, UPCs & expiration codes

Lot #: Product code 2B0973: P279935, Exp 7/13

Where it was sold

Nationwide & Puerto Rico

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-627-2013
Classification
Class II
Status
Terminated
Recall initiated
May 21, 2013
FDA report date
Jul 10, 2013
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
Baxter Healthcare Corp.

Original FDA data

Every field from FDA enforcement report D-627-2013, exactly as published.

Show all FDA fields
City
Deerfield
State
IL
Status
Terminated
Country
United States
Event ID
65288
Address
1 Baxter Pkwy
Code information
Lot #: Product code 2B0973: P279935, Exp 7/13
Postal code
60015-4625
Report date
Jul 10, 2013
Product type
Drugs
Recall number
D-627-2013
Classification
Class II
Recalling firm
Baxter Healthcare Corp.
Termination date
Jun 18, 2015
Reason for recall
Lack of Assurance of Sterilty: Specific lot numbers of these products have been identified for potential administration port leakage. The potential for leakage is the result of a manufacturing issue which occurred during the sealing of the closure assembly at the administration port.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Lidocaine Hydrochloride and 5% Dextrose Injection, USP, 2g VIAFLEX Plus Plastic Container, 500mL, Rx Only, Baxter, Deerfield, IL 60015
Distribution pattern
Nationwide & Puerto Rico
Recall initiation date
May 21, 2013
Initial firm notification
Letter
Center classification date
Jun 28, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-627-2013, published Jul 10, 2013. View the source record (openFDA) · FDA enforcement reports

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

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