Fresh Recalls

FDAClass II · Drug · Recall D-0591-2026 · Recalled June 24, 2026

VistaPharm recall — PAI Holdings LLC

Agency report date: June 24, 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
VistaPharm
Company / brand
PAI Holdings
Lot / serial / date codes
Lot #: AE006, expires: 5/31/2026
Distribution
U.S.A. Nationwide
Agency product description and boundaries

VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in 120 mL (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-04.

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: Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

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: VistaPharm

3. Open the official notice or contact

Official recall ID
D-0591-2026
Brand
PAI Holdings
Classification
Class II
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Greenville, SC, United States
Firm address
1700 Perimeter Rd, 29605-5252

Identifying details (verbatim from the notice)

Product codes / lots
Lot #: AE006, expires: 5/31/2026
Distribution
U.S.A. Nationwide
Firm notified the public via
Letter
FDA event ID
99000
Recall initiated
May 15, 2026
FDA classified
June 12, 2026
FDA report date
June 24, 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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