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FDA recall, , Moderate risk

Central Admixture Pharmacy Services Pediatric Total Parenteral Nutrition Bags

The Total Parental Nutrition bag lacks copper and famotidine as labeled.

What happened

Central Admixture Pharmacy Services, Inc., of Woburn, Massachusetts, recalled Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, Rx# 24-1269856-0-1, Compound Volume 1295 mL per bag, because the bag did not contain copper and famotidine per label. The recall began June 2, 2026, and was added to the FDA's Enforcement Report on June 24, 2026.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:

  1. Check the FDA or company notice for instructions specific to this product.
  2. Ask your pharmacist or doctor whether your lot is affected and what to do.

Is your bag affected?

Compare the details below with your product and check the FDA notice to confirm whether it is affected.

  1. Product details

    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.

Recall details

Company began the recall
Company
Central Admixture Pharmacy Services, Inc.Woburn, Massachusetts
Risk

Moderate risk

Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

Event ID
99265
Recall number
D-0618-2026

All recalls from Central Admixture Pharmacy Services, Inc.

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. Listed on Recall Canary

  4. In FDA's weekly enforcement report

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 3, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)