FDA Device recall Z-2537-2017
Clarke-Reich Laparoscopic Knot Pusher
- FDA Device
- Class II
- terminated
- Published 2017-06-21
On 2017-06-21 the FDA classified a Class II recall of Clarke-Reich Laparoscopic Knot Pusher 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-2537-2017 |
| 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
Clarke-Reich Laparoscopic Knot Pusher
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-CRKP-042900 |
|---|
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-2537-2017%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.