CLASS II Drug recall · Reported 27 Nov 2019 · FDA Enforcement Report
Perrigo Neomycin and Polymixin B Sulfates recalled
Altaire Pharmaceuticals is recalling Perrigo Neomycin and Polymixin B Sulfates and Dexamethasone Ophthalmic Ointment, Net, distributed nationwide in the US. The recall was initiated on 2 Jul 2019 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0352-2020
- FDA event ID
- 83265
- Recalling firm
- Altaire Pharmaceuticals, Aquebogue, NY
- Classification
- Class II
- Status
- Completed
- Recall initiated
- 2 Jul 2019
- FDA classified
- 15 Nov 2019
- Reported
- 27 Nov 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Sterility
- Drug class
- Eye Drops
Timeline
| 2 Jul 2019 | Recall initiated by company | |
| 15 Nov 2019 | Classified by FDA | +136 days |
| 27 Nov 2019 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of Assurance of Sterility
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Perrigo Neomycin and Polymixin B Sulfates and Dexamethasone Ophthalmic Ointment, Net. Wt 3.5 gm, Sterile, Rx only, Manufactured for Perrigo Minneapolis, MN 55427, NDC 0574-4160-35
Where it was distributed
U.S.A. Nationwide
Questions about this recall
Why was it recalled?
Lack of Assurance of Sterility
Which lots are affected?
Lot #: RGC, Exp 7/19; RHB, RHC, Exp 8/19; RID, RIC, RIG, Exp 9/19; RKH, RKI, RKJ, RKK, RKL, Exp 11/19; RLM, Exp 12/19; SAI, Exp 1/20; SBG, SBH, Exp 2/20; SCF, Exp 3/20, SEA, Exp 5/20; SFA, SFB, Exp 6/20; SHA, Exp 8/20; SIB, Exp 9/20; SJC, Exp 10/20; TAB, TAF, Exp 1/21; TBP, TBQ, Exp 2/21; TCV, TCW, Exp 3/21
Where was it sold?
U.S.A. Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
100 other products · FDA event 83265This product is part of a recall event; the main page for the event is CVS Health Redness Relief Lubricant Redness Reliever Eye recalled.
More recalls from Altaire Pharmaceuticals
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|---|---|---|---|---|---|
| Drug | CLASS II | Altacaine (Tetracaine Hydrochloride) Ophthalmic Solution recalled | Altaire Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Altaire Sterile Eye Wash, Altaire Pharmaceuticals recalled | Altaire Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | OCuSOFT Tetravisc Tetracaine HCl 0.5% Sterile Anesthetic Single Dose recalled | Altaire Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Walgreens Sodium Chloride Ophthalmic Solution recalledSodium Chloride | Altaire Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | ActivEyes Altachlore Solution recalled by Altaire PharmaceuticalsAltachlore Sodium Chloride Hypertonicity | Altaire Pharmaceuticals | Sterility | Nationwide |