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Class II: temporary or reversible health riskTerminated

Pentec Health Baxter LL bag 1% Amino Acids Recall

Baxter LL bag 1% Amino Acids (Intraperitoneal Parenteral Nutrition - dialysate solution…

Pentec Health · Boothwyn, PA

Risk level
Class II
Reported by FDA
Jun 12, 2013
Recall ID
D-583-2013
Check your lot numberHow we source this data

Summary

Pentec Health recalled Baxter LL bag 1% Amino Acids starting May 15, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-583-2013 on Jun 12, 2013. Reason: Lack of Assurance of Sterility: Sterility could not be assured for compounded sterile renal nutritional prescriptions. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: Sterility could not be assured for compounded sterile renal nutritional prescriptions.

Product description

Baxter LL bag 1% Amino Acids (Intraperitoneal Parenteral Nutrition - dialysate solution with added amino acids), in a) 3000mL bag, b) 5000mL bag and c) 6000mL bag, Pentec Health Inc., 4 Creek Parkway Suite A, Boothwyn, PA 19061-3132

Lot numbers, UPCs & expiration codes

a) Compounding Date: 04/30/13 Discard After: 05/21/13 b) Compounding Date: 04/30/13 Discard After: 05/21/13 c) Compounding Date: 04/25/13, 04/30/13 Discard After: 05/16/13, 05/21/13

Where it was sold

Dialysis Centers Direct to patient

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-583-2013
Classification
Class II
Status
Terminated
Recall initiated
May 15, 2013
FDA report date
Jun 12, 2013
Quantity
5 Bags
Recall type
Voluntary: Firm initiated
Recalling firm
Pentec Health

Original FDA data

Every field from FDA enforcement report D-583-2013, exactly as published.

Show all FDA fields
City
Boothwyn
State
PA
Status
Terminated
Country
United States
Event ID
65180
Address
4 Creek Pkwy Ste A
Code information
a) Compounding Date: 04/30/13 Discard After: 05/21/13 b) Compounding Date: 04/30/13 Discard After: 05/21/13 c) Compounding Date: 04/25/13, 04/30/13 Discard After: 05/16/13, 05/21/13
Postal code
19061-3132
Report date
Jun 12, 2013
Product type
Drugs
Recall number
D-583-2013
Classification
Class II
Recalling firm
Pentec Health
Product quantity
5 Bags
Termination date
Dec 16, 2014
Reason for recall
Lack of Assurance of Sterility: Sterility could not be assured for compounded sterile renal nutritional prescriptions.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Baxter LL bag 1% Amino Acids (Intraperitoneal Parenteral Nutrition - dialysate solution with added amino acids), in a) 3000mL bag, b) 5000mL bag and c) 6000mL bag, Pentec Health Inc., 4 Creek Parkway Suite A, Boothwyn, PA 19061-3132
Distribution pattern
Dialysis Centers Direct to patient
Recall initiation date
May 15, 2013
Initial firm notification
Telephone
Center classification date
Jun 6, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-583-2013, published Jun 12, 2013. View the source record (openFDA) · FDA enforcement reports

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

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