CURAD recallZ-0903-2026 · Medline Industries, LP · initiated Oct 27, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was 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.
FDA root cause category: Package design/selection
What the company is doing
Medline Industries issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 10/27/2025 via email and USPS first class mail. The notices explained the issue, potential risk, and requested the following: "REQUIRED ACTION: 1.Immediately check your stock for the affected item number(s) and the affected lot number(s) listed within the recall portal. Quarantine all affected product. Upon completion of the below actions, please destroy affected product. 2.Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the response form. Website link: https://recalls.medline.com Recall Reference #: R-25-220 Recall Code: 3.Your account will receive credit once the response form is submitted. 4.If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please request that customers destroy any affected product. You should include your customers quantities on your response form." For questions, contact the Recall Department at 866-359-1704 or [email protected].
Recall details
- Recall number
- Z-0903-2026
- Status
- Open, Classified
- Initiated by the company
- Oct 27, 2025
- Posted by the FDA
- Dec 11, 2025
- Recalling firm
- Medline Industries, LP
- Quantity
- 6,989,900 units
- Product code
- KGX
- Distribution
- US, Guam, Canada, United Arab Emirates
Product description
Quick Strip Fabric Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25650QS
Code information (models, lots, serial numbers)
UDI/DI 10888277699410 (each), 20888277699417 (box), 30888277699414 (case); ALL LOTS
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- CURAD NON25650QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall1 report
Product lines
Other products in the same recall event
The FDA groups related products into one recall event (event 97978).
- Z-0900-2026 · Open, ClassifiedQuick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS
- Z-0901-2026 · Open, ClassifiedQuick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25600QS
- Z-0902-2026 · Open, ClassifiedFur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON256133QS
- Z-0904-2026 · Open, ClassifiedQuick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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