CLASS II ONGOING Drug recall · Reported 26 Mar 2025 · FDA Enforcement Report
Curad Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents recalled
MEDLINE INDUSTRIES, LP - Northfield is recalling Curad Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per, 30, Single Use, distributed nationwide in the US. The recall was initiated on 17 Feb 2025 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-0289-2025
- FDA event ID
- 96404
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL
- Manufacturer
- Medline Industries, LP
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 17 Feb 2025
- FDA classified
- 20 Mar 2025
- Reported
- 26 Mar 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Sterility
Timeline
| 17 Feb 2025 | Recall initiated by company | |
| 20 Mar 2025 | Classified by FDA | +31 days |
| 26 Mar 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Subpotent Drug
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
CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per Case, Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093, USA, Made in India, www.curad.com, 1-800-633-5463, NDC 53329-827-30.
Where it was distributed
Nationwide
Questions about this recall
Is Curad Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per, 30, Single Use recalled?
Yes. MEDLINE INDUSTRIES, LP - Northfield recalled Curad Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per, 30, Single Use on 17 Feb 2025. The recall is Class II and its status is Ongoing. Recall number D-0289-2025.
Why was it recalled?
Subpotent Drug
Which lots are affected?
SKU: CUR090737RB, Lot: 61224050002
Where was it sold?
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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Other Isopropyl Alcohol recalls
All 11| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Hand Sanitizing Wipes (Benzalkonium Chloride 13%) recalledFirst Aid Only Hand Sanitizing Wipe | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | H-e-b, inControl, Sterile* Alcohol Pads, Cont recalledIncontrol Alcohol | MEDLINE INDUSTRIES, LP - Northfield | Sterility | Nationwide |
| Drug | CLASS II | Rite Aid Pharmacy, first aid alcohol prep pads recalledAlcohol | MEDLINE INDUSTRIES, LP - Northfield | Potency & Assay | Nationwide |
| Drug | CLASS II | Medline Alcohol Prep Pads, 70% Isopropyl Alcohol recalledMedline Alcohol Prep | MEDLINE INDUSTRIES, LP - Northfield | Sterility | Nationwide |
| Drug | CLASS II | ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs recalledWalmart | MEDLINE INDUSTRIES, LP - Northfield | Sterility | Nationwide |