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Class I: serious health riskTerminated

Baxter Healthcare Clinimix E 4 Recall

Clinimix E 4

Baxter Healthcare Corp. · Deerfield, IL

Risk level
Class I
Reported by FDA
Mar 26, 2014
Recall ID
D-1159-2014
Check your lot numberHow we source this data

Summary

Baxter Healthcare recalled Clinimix E 4 starting Nov 18, 2013. The FDA classified it as Class I (serious health risk) and published enforcement report D-1159-2014 on Mar 26, 2014. Reason: Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose. Status: Terminated.

Why it was recalled

Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.

Product description

Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in 10% Dextrose with Calcium) Injection, 2000 mL CLARITY Dual Chamber Container bag, Rx only. Dist: Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC 0338-1115-04.

Lot numbers, UPCs & expiration codes

Lot#: P275883, Exp 10/2013

Where it was sold

US Nationwide

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-1159-2014
Classification
Class I
Status
Terminated
Recall initiated
Nov 18, 2013
FDA report date
Mar 26, 2014
Quantity
7,068 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Baxter Healthcare Corp.

Original FDA data

Every field from FDA enforcement report D-1159-2014, exactly as published.

Show all FDA fields
City
Deerfield
State
IL
Status
Terminated
Country
United States
Event ID
67107
Address
1 Baxter Pkwy
Code information
Lot#: P275883, Exp 10/2013
Postal code
60015-4625
Report date
Mar 26, 2014
Product type
Drugs
Recall number
D-1159-2014
Classification
Class I
Recalling firm
Baxter Healthcare Corp.
Product quantity
7,068 bags
Termination date
Sep 20, 2016
Reason for recall
Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in 10% Dextrose with Calcium) Injection, 2000 mL CLARITY Dual Chamber Container bag, Rx only. Dist: Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC 0338-1115-04.
Distribution pattern
US Nationwide
Recall initiation date
Nov 18, 2013
Initial firm notification
Letter
Center classification date
Mar 14, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1159-2014, published Mar 26, 2014. View the source record (openFDA) · FDA enforcement reports

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

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