Fresh Recalls

FDAClass II · Drug · Recall D-0618-2026 · Recalled July 1, 2026

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag recall — Central Admixture Pharmacy Services, Inc.

Agency report date: July 1, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag
Company / brand
Central Admixture Pharmacy Services
Lot / serial / date codes
24-1269856-0-1
Distribution
MA
Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag

3. Open the official notice or contact

Official recall ID
D-0618-2026
Brand
Central Admixture Pharmacy Services
Classification
Class II
Units affected
One (1) patient-specific TPN prescription.
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Woburn, MA, United States
Firm address
55 6th Rd, N/A, 01801-1767

Identifying details (verbatim from the notice)

Product codes / lots
24-1269856-0-1
Distribution
MA
Firm notified the public via
N/A
FDA event ID
99265
Recall initiated
June 2, 2026
FDA classified
June 24, 2026
FDA report date
July 1, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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