RecallHawk
Class II Recall

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Rx# 24-1269856-0-1Compound Volume

Central Admixture Pharmacy Services, Inc.

Summary

The FDA issued a Class II for Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient speci by Central Admixture Pharmacy Services, Inc.. Reason: Incorrect product formulation: bag did not contain copper and famotidine per label..

Details

Source

Drug Recall

External ID

D-0618-2026

Action Date

2026-07-01

Status

Ongoing

Category

drug

Product Description

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Rx# 24-1269856-0-1Compound Volume 1295 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Boston, 55 6th Rd Woburn, Massachusetts 01801-1767.

Lot/Code Info: 24-1269856-0-1

Quantity Affected: One (1) patient-specific TPN prescription.

Reason for Recall

Incorrect product formulation: bag did not contain copper and famotidine per label.

Distribution

MA

Type: Voluntary: Firm initiated

Recall Initiated: 2026-06-02

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 49 drug recalls issued in the same week, part of 81 drug-related FDA actions this month.

Central Admixture Pharmacy Services, Inc. has 308 FDA actions in our database, including 308 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 308 FDA actions in our database, including 308 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0618-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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