FDA Device recall Z-0946-2025
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE HEGAR DILATOR 11&12MM STRLCS25Model Number 96-0960
- FDA Device
- Class II
- ongoing
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE HEGAR DILATOR 11&12MM STRLCS25Model Number 96-0960 by Sklar Instruments, citing reports of various packaging issues that may result in a breach of the sterile barrier.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0946-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-12-03 |
| Published | 2025-01-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Sklar Instruments |
| Distribution | US |
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE HEGAR DILATOR 11&12MM STRLCS25Model Number 96-0960; 2) ECONO STERILE HEGAR DILATOR 9&10MM STRL CS25Model Number 96-0961; 3) ECONO STERILE HEGAR DILATOR 7&8MM STRL CS25Model Number 96-0962; 4) ECONO STERILE HEGAR DILATOR 5&6MM STERL CS25Model Number 96-0963; 5) ECONO STERILE HEGAR DILATOR 3&4MM STERL CS25Model Number 96-0964; 6) ECONO STERILE HEGAR DILATOR 1&2MM STERL CS25Model Number 96-0965; 7) ECONO STERILE HANK DILATOR 5.5&6MM STRL CS25Model Number 96-0966; gynecological dilators
Reason
Reports of various packaging issues that may result in a breach of the sterile barrier.
Identifiers
| code_info | 1) 96-0960, UDI/DI 50649111474796, Lot codes: FSS5; 2) 96-0961, UDI/DI 50649111474802, Lot codes: FSS5; 3) 96-0962,…1) 96-0960, UDI/DI 50649111474796, Lot codes: FSS5; 2) 96-0961, UDI/DI 50649111474802, Lot codes: FSS5; 3) 96-0962, UDI/DI 50649111474819, Lot codes: FSS5; 4) 96-0963, UDI/DI 50649111474826, Lot codes: FSS5; 5) 96-0964, UDI/DI 50649111474833, Lot codes: FSS5; 6) 96-0965, UDI/DI 50649111474840, Lot codes: FSS5; 7) 96-0966, UDI/DI 50649111474857, Lot codes: SK-119. |
|---|
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-0946-2025%22
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