CLASS II ONGOING Drug recall · Reported 1 Jul 2026 · FDA Enforcement Report
Total Parental Nutrition - Pediatric PN Patient-Specific recalled
Central Admixture Pharmacy Services is recalling Total Parental Nutrition - Pediatric PN Patient-Specific TPN, (patient specific), Rx#, distributed in Massachusetts. The recall was initiated on 2 Jun 2026 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0618-2026
- FDA event ID
- 99265
- Recalling firm
- Central Admixture Pharmacy Services, Woburn, MA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 2 Jun 2026
- FDA classified
- 24 Jun 2026
- Reported
- 1 Jul 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Packaging Defects
- Drug class
- Injectable & IV Drugs
Timeline
| 2 Jun 2026 | Recall initiated by company | |
| 24 Jun 2026 | Classified by FDA | +22 days |
| 1 Jul 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Incorrect product formulation: bag did not contain copper and famotidine per label.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
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.
Where it was distributed
MA
Questions about this recall
Why was it recalled?
Incorrect product formulation: bag did not contain copper and famotidine per label.
Which lots are affected?
24-1269856-0-1
Where was it sold?
MA
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Central Admixture Pharmacy Services
All 347| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Total Parental Nutrition - Pediatric PN Patient-Specific recalled | Central Admixture Pharmacy Services | Packaging Defects | GA |
| Drug | CLASS I | PHENYLephrine added to 0.9% sodium chloride, 40 mg/* (160 mcg/mL) recalled | Central Admixture Pharmacy Services | Particulate Matter | Nationwide |
| Drug | CLASS II | HYDROmorphone in dextrose 5%, 3 mg/, (0.1 mg/mL) Syringe recalled | Central Admixture Pharmacy Services | Sterility | Nationwide |
| Drug | CLASS II | fentaNYL in 0.9% sodium chloride, 1,000 mcg/, (10 mcg/mL) recalled | Central Admixture Pharmacy Services | Sterility | Nationwide |
| Drug | CLASS II | rocuronium, 50 mg/, (10 mg/mL) Syringe recalled | Central Admixture Pharmacy Services | Sterility | Nationwide |