FDA Device recall Z-1548-2022
Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708
- FDA Device
- Class II
- terminated
- Published 2022-08-24
On 2022-08-24 the FDA classified a Class II recall of Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708 by Trinity Sterile, citing kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1548-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-06-29 |
| Published | 2022-08-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Trinity Sterile |
| Distribution | US |
Product
Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708
Reason
Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy
Identifiers
| code_info | UDI-DI Number: 50649111317590 Case 10649111317590 Kit Lot Numbers: 600001 600002 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1548-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.