FDA Device recall Z-1835-2024
CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Model 44102, Sterile, Hypoallergenic
- FDA Device
- Class II
- ongoing
- Published 2024-05-22
On 2024-05-22 the FDA classified a Class II recall of CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Model 44102, Sterile, Hypoallergenic by Cardinal Health 200, citing potential contamination of the product with latex adhesive residual.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1835-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-17 |
| Published | 2024-05-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Cardinal Health 200 |
| Distribution | US |
Product
CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Model 44102, Sterile, Hypoallergenic.
Reason
Potential contamination of the product with latex adhesive residual.
Identifiers
| code_info | Lot #A14722, UDI-DI: 50192253049907 (CS), 20192253049906 (BX) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1835-2024%22
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