Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts
Class III · Low risk Ongoing Initiated Jul 27, 2023 (3 years ago)

Tobramycin Opthalmic Solution USP (Tobramycin Ophthalmic Solution)

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Impurities/Degradation Specifications

Cause type: Impurity / degradation

An impurity or degradation product above its limit - other than nitrosamines. Unexpected substances in a batch can make it unsafe or less effective, even when the active ingredient is present. All impurity / degradation recalls.

What was recalled

Tobramycin Opthalmic Solution USP, 0.3%, 5mL bottle, Rx only, Manufactured for: Alembic Pharmaceuticals, Bedminster, NJ 07921, USA, NDC 62332-518-05

Affected NDC 62332-0518-05

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

Drug: Tobramycin

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Tobramycin Ophthalmic Solution
NDC 62332-0518
TOBRAMYCIN 3 mg/mL Solution/ Drops
Ophthalmic
Alembic Pharmaceuticals Inc. Rx
Recalling firm
Alembic Pharmaceuticals, INC.
NDC code
62332-518-05
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1086-2023 · FDA notice

Low risk, still worth a check. Class III means the product is unlikely to cause harm but breaks an FDA rule (often labeling). If your lot matches, your pharmacy will normally swap it; there is no need for alarm.

Other Tobramycin recalls

See all
Class II · Moderate risk

Tobramycin for Injection

Failed Stability Specification: Water determination was found not complying with specification.

Terminated Stability / shelf life Eugia US LLC NDC 55150-470-06 D-0385-2024

Other recalls by Alembic Pharmaceuticals, INC.

All 2023 recalls
Class II · Moderate risk

Bromfenac Ophthalmic Solution 0.07%

Failed Impurities/Degradation Specifications: out of specification at the time of testing i.e. 20th month stability testing.

Ongoing Impurity / degradation Alembic Pharmaceuticals, INC. NDC 62332-583-03 Recall number pending
Class III · Low risk

Fesoterodine Fumarate

Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.

Ongoing Impurity / degradation Alembic Pharmaceuticals Limited NDC 62332-176-30 D-0248-2026
Class III · Low risk

Fesoterodine Fumarate

Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.

Ongoing Impurity / degradation Alembic Pharmaceuticals Limited NDC 62332-175-30 D-0156-2026
Class II · Moderate risk

Doxepin Hydrochloride Capsules

CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.

Ongoing Nitrosamine impurity Alembic Pharmaceuticals Limited NDC 62332-637-31 D-0566-2025