FDA Device recall Z-2535-2017
Pereyra Ligature Carrier 75
- FDA Device
- Class II
- terminated
- Published 2017-06-21
On 2017-06-21 the FDA classified a Class II recall of Pereyra Ligature Carrier 75 by Cook, citing reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2535-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-25 |
| Published | 2017-06-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Cook |
| Distribution | US |
Product
Pereyra Ligature Carrier 75
Reason
reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products
Identifiers
| code_info | All lots Catalog numbers J-PLC-751810 and 090100 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2535-2017%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.