Z-1835-2024 Class II Ongoing
FDA device recall Z-1835-2024 was initiated by Cardinal Health 200, LLC on Apr 17, 2024 and is designated Class II. Reason for recall: Potential contamination of the product with latex adhesive residual. The recall status is ongoing. Affected quantity: 2,000 packages.
Recall Details
- Product Type
- Devices
- Report Date
- May 22, 2024
- Initiation Date
- Apr 17, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,000 packages
Product Description
CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Model 44102, Sterile, Hypoallergenic.
Reason for Recall
Potential contamination of the product with latex adhesive residual.
Distribution Pattern
US Nationwide distribution.
Code Information
Lot #A14722, UDI-DI: 50192253049907 (CS), 20192253049906 (BX)
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1835-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026