UnratedDrug recall · FDA · Published July 16, 2026
Central Admixture Pharmacy Services recalls pediatric TPN bags with incorrect formulation
Central Admixture Pharmacy Services recalls pediatric TPN bags with incorrect formulation. Patients may face health risks from improper nutrition mixtures. Contact for details.
“Central Admixture Pharmacy Services recalls pediatric TPN bags with incorrect formulation.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/309282-central-admixture-pharmacy-services-recalls-pediatric-tpn-bags-with-incorrect. Based on FDA recall #D-0740-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0740-2026%22&limit=1).
The FDA announced on July 16, 2026, that Central Admixture Pharmacy Services Inc. is recalling pediatric Total Parental Nutrition bags due to incorrect product formulation. The agency classified the recall as Class III.
How to tell if you have it
Brand: Central Admixture Pharmacy Services
Product: Pediatric PN Patient-Specific TPN Bag, Compound Volume 416.8 mL per bag
Lot Codes: 20-1535990-0-1 and 20-1535892-0-1
Expiration Date: 16 July 2026
Distribution: Georgia only
The hazard
The recall addresses incorrect product formulation in the pediatric Total Parental Nutrition bags. The FDA classified the issue as a Class III hazard.
Context
GovInfoNow's records show Central Admixture Pharmacy Services, Inc. has had 9 other recalls on record since May 28, 2014. Other recent recalls of similar products include CAPS TPN Bag Recall: Incorrect Insulin Formulation Risk (Dec. 27, 2025) and American Health Packaging Buprenorphine Tablets Recall: Label Mix-Up Hazard (Aug. 19, 2026).
How to tell if you have this one
Check for the lot numbers 20-1535990-0-1 and 20-1535892-0-1 on the bags. These bags were sold with an expiration date of July 16, 2026.
Brand
Central Admixture Pharmacy Services
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Bag Lot Number
Look for lot numbers 20-1535990-0-1 or 20-1535892-0-1 on the TPN bag.
Where it went and when
Where it was distributed
Distributed in Georgia.
Listed by the agency
Not listed
FDA distribution: “GA only” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Georgia.
Recall timeline
FDA published this recall 27 days after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
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-0740-2026 (July 16, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0740-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.