Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts
Class II · Moderate risk Completed Initiated Jul 2, 2019 (7 years ago)

Altaire Homatropaire Homatropine Hyrdobromide Opthalmic Solution (Homatropine Hydrobromide)

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility

Cause type: Sterility / contamination

A product that must be sterile could not be assured sterile, or was contaminated. A top reason for injectables, eye drops and IV products - loss of sterility assurance can lead to serious infections. All sterility / contamination recalls.

What was recalled

Altaire Homatropaire Homatropine Hyrdobromide Opthalmic Solution, USP, 5 %, 5 mL, Sterile, Rx only, Mfd. by: Altaire Pharmaceuticals, Inc. Aquebogue, NY 11931, NDC 59390-192-05

Affected NDC 59390-0192-05

Compare with the code on your package — it is the most precise check available.

Drug: Atropine

Recalling firm
Altaire Pharmaceuticals, Inc.
NDC code
59390-192-05
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0455-2020 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now completed, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Atropine recalls

See all
Class II · Moderate risk

Atropine Sulfate injection

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

Ongoing Particulate / foreign matter American Regent, Inc. NDC 0517-1001-01 D-0795-2026

Other recalls by Altaire Pharmaceuticals, Inc.

All 2019 recalls