Fresh Recalls

FDAClass II · Drug · Recall D-0548-2026 · Recalled May 27, 2026

fentaNYL Citrate recall — IntegraDose Compounding Services LLC

Agency report date: May 27, 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
fentaNYL Citrate
Company / brand
IntegraDose Compounding Services
Lot / serial / date codes
Lot#: 20260310FEN-1, Exp. Date: 09/06/2026
Distribution
Nationwide.
Agency product description and boundaries

fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3650 Victorie St N, Suite 900, Shoreview, MN, NDC 71139-6030-1.

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: Subpotent Drug

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: fentaNYL Citrate

3. Open the official notice or contact

Official recall ID
D-0548-2026
Brand
IntegraDose Compounding Services
Classification
Class II
Units affected
376 cassettes
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Shoreview, MN, United States
Firm address
3650 Victoria St N Ste 900, 55126-2906

Identifying details (verbatim from the notice)

Product codes / lots
Lot#: 20260310FEN-1, Exp. Date: 09/06/2026
Distribution
Nationwide.
FDA event ID
98991
Recall initiated
May 12, 2026
FDA classified
May 21, 2026
FDA report date
May 27, 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 August 25, 2026 at 6:00 PM UTC.

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