Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Compound Volume 416.8 mL per bag,
Summary
The FDA issued a Class III for Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient speci by Central Admixture Pharmacy Services Inc. Reason: Incorrect Product Formulation.
Details
Source
Drug Recall
External ID
D-0740-2026
Action Date
2026-08-12
Status
Ongoing
Category
drug
Product Description
Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Compound Volume 416.8 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Inc., Atlanta, 1750 Corp Dr. Ste 725, Norcross, GA 30093 (844) 903-6418
Lot/Code Info: Lot #: 20-1535990-0-1 & 20-1535892-0-1, Exp. Date 16 July 2026
Quantity Affected: (2) patient-specific TPN prescriptions
Reason for Recall
Incorrect Product Formulation
Distribution
GA only
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-16
Company
Norcross, GA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 11 drug recalls issued in the same week, part of 59 drug-related FDA actions this month.
Central Admixture Pharmacy Services Inc has 309 FDA actions in our database, including 309 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Central Admixture Pharmacy Services Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Central Admixture Pharmacy Services Inc have FDA actions?
Central Admixture Pharmacy Services Inc has 309 FDA actions in our database, including 309 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0740-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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