Central Admixture Pharmacy Services recalls pediatric TPN bags with incorrect formulation
Central Admixture Pharmacy Services recalls pediatric TPN bags that lack copper and famotidine as labeled, potentially causing unsafe nutrition delivery.
“Central Admixture Pharmacy Services recalls pediatric TPN bags with incorrect formulation.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/31237-central-admixture-pharmacy-services-recalls-pediatric-tpn-bags-with-incorrect. Based on FDA recall #D-0618-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0618-2026%22&limit=1).
The FDA announced on June 2, 2026, that Central Admixture Pharmacy Services is recalling one patient-specific Total Parental Nutrition bag due to an incorrect formulation that lacked copper and famotidine as labeled. This Class II recall affects a single prescription distributed in Massachusetts.
How to tell if you have it
Brand: Central Admixture Pharmacy Services
Product: Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag
Rx#: 24-1269856-0-1
Volume: 1295 mL
Location: Boston/Woburn, Massachusetts
The hazard
The bag did not contain copper and famotidine per the label. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Central Admixture Pharmacy Services has nine other recalls on record since May 28, 2014. Other recent recalls of similar products include CAPS Lidocaine 2% Syringe Recall (Sept. 21, 2023), Phenylephrine IV Bags with Particulate Matter (Feb. 20, 2025), and pediatric TPN bags with incorrect formulation (July 16, 2026). Other recent recalls of similar products include CAPS TPN Bag Recall (Dec. 27, 2025), Fagron Recalls Tropicamide Eye Drops (Nov. 20, 2025), and Amneal Magnesium Sulfate IV Bags (March 18, 2026).
How to tell if you have this one
Check for the product code 24-1269856-0-1 on the bag. These bags were sold with a specific prescription number and are intended for pediatric patients only.
Brand
Central Admixture Pharmacy Services
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the product code 24-1269856-0-1 on the bag to confirm it is recalled.
Where it went and when
Where it was distributed
Distributed in Massachusetts.
Listed by the agency
Not listed
FDA distribution: “MA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Massachusetts.
Recall timeline
FDA published this recall 29 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #D-0618-2026 (June 2, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0618-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.