CLASS II ONGOING Device recall · Reported 17 Dec 2025 · FDA Enforcement Report
Quick Strip Plastic Sterile Adhesive Bandages, 75" x 3", Medline recalled
Medline Industries is recalling Quick Strip Plastic Sterile Adhesive Bandages, 75" x 3", Medline. The recall was initiated on 27 Oct 2025 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0900-2026
- FDA event ID
- 97978
- Recalling firm
- Medline Industries, Northfield, IL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 27 Oct 2025
- FDA classified
- 11 Dec 2025
- Reported
- 17 Dec 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Foreign Material
- Device type
- Other Medical Devices
Timeline
| 27 Oct 2025 | Recall initiated by company | |
| 11 Dec 2025 | Classified by FDA | +45 days |
| 17 Dec 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
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS
Where it was distributed
US, Guam, Canada, United Arab Emirates
Questions about this recall
Is Quick Strip Plastic Sterile Adhesive Bandages, 75" x 3", Medline recalled?
Yes. Medline Industries recalled Quick Strip Plastic Sterile Adhesive Bandages, 75" x 3", Medline on 27 Oct 2025. The recall is Class II and its status is Ongoing. Recall number Z-0900-2026.
Why was it recalled?
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
Which lots are affected?
UDI/DI 10888277699397 (each), 20888277699394 (box), 30888277699391 (case); ALL LOTS
Where was it sold?
US, Guam, Canada, United Arab Emirates
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
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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