Z-0900-2026Class II

Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS

Name: Z-0900-2026 Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS
Creator: Medline Industries, LP
Published: 2025-10-27
License: https://open.fda.gov/license/

MEDLINE INDUSTRIES, LP - Northfield / initiated 2025-10-27 / Open, Classified / root cause: packaging

FDA source

Medline Industries, LP began a recall of Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS on 2025-10-27. FDA classified it as Class II and gives the reason as "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". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0900-2026
Classification: Class II
Status: Open, Classified
Initiated: 2025-10-27
Posted: 2025-12-11
Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product: Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS
Product code: KGX Tape And Bandage, Adhesive
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.
Root cause tag: packaging
FDA root cause: Package design/selection
Action: 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].
Quantity in commerce: 1,725,600 units
Distribution: US, Guam, Canada, United Arab Emirates
Product codes and lots: UDI/DI 10888277699397 (each), 20888277699394 (box), 30888277699391 (case); ALL LOTS

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0900-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0898-2026	Class II	Ongoing	Voluntary: Firm initiated	2025-12-17	2025-12-11
Z-0899-2026	Class II	Ongoing	Voluntary: Firm initiated	2025-12-17	2025-12-11
Z-0900-2026	Class II	Ongoing	Voluntary: Firm initiated	2025-12-17	2025-12-11
Z-0901-2026	Class II	Ongoing	Voluntary: Firm initiated	2025-12-17	2025-12-11
Z-0902-2026	Class II	Ongoing	Voluntary: Firm initiated	2025-12-17	2025-12-11
Z-0903-2026	Class II	Ongoing	Voluntary: Firm initiated	2025-12-17	2025-12-11
Z-0904-2026	Class II	Ongoing	Voluntary: Firm initiated	2025-12-17	2025-12-11

Product code KGX

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)