Tobramycin for Injection
Failed Stability Specification: Water determination was found not complying with specification.
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
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.
Tobramycin Opthalmic Solution USP, 0.3%, 5mL bottle, Rx only, Manufactured for: Alembic Pharmaceuticals, Bedminster, NJ 07921, USA, NDC 62332-518-05
Compare with the code on your package — it is the most precise check available.
Drug: Tobramycin
From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.
| Product | Strength | Form & route | Labeler | Type |
|---|---|---|---|---|
| Tobramycin Ophthalmic Solution NDC 62332-0518 |
TOBRAMYCIN 3 mg/mL | Solution/ Drops Ophthalmic |
Alembic Pharmaceuticals Inc. | Rx |
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.
Failed Stability Specification: Water determination was found not complying with specification.
CGMP Deviations: Firm went out of business and could no longer continue stability studies.
CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Lack of sterility assurance
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Failed Impurities/Degradation Specifications: out of specification at the time of testing i.e. 20th month stability testing.
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
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