Fresh Recalls

FDAClass III · Drug · Recall D-0835-2026 · Recalled September 16, 2026

Povidone Iodine 1 recall — ImprimisRx NJ LLC

Agency report date: September 16, 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
Povidone Iodine 1
Company / brand
ImprimisRx NJ
Lot / serial / date codes
Lot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026
Distribution
USA Nationwide
Agency product description and boundaries

Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-732-10

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 III: not likely to cause adverse health consequences.

Affected product: Povidone Iodine 1 recall status

3. Open the official notice or contact

Official recall ID
D-0835-2026
Brand
All ImprimisRx NJ recalls
Classification
Class III
Units affected
772 bottles
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Ledgewood, NJ, United States
Firm address
1705 Us Highway 46 Ste 4, 07852-9720

Identifying details (verbatim from the notice)

Product codes / lots
Lot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026
Distribution
USA Nationwide
Firm notified the public via
Letter
FDA event ID
99756
Recall initiated
August 24, 2026
FDA classified
September 8, 2026
FDA report date
September 16, 2026

Other drug recalls from around the same time

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 October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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