FDA Device recall Z-3222-2017
Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft t…
- FDA Device
- Class II
- terminated
- Published 2017-10-04
On 2017-10-04 the FDA classified a Class II recall of Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft t… by Teleflex Medical, citing for some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3222-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-19 |
| Published | 2017-10-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Teleflex Medical |
| Distribution | AL, AZ, CA, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MN, MO, NC, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV |
Product
Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips to soft tissue during laparoscopic surgery.
Reason
For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
Identifiers
| code_info | Lot #'s: 73D1600174, 73D1600587, 73E1600661, 73F1600015, 73G1600729, 73H1600012, 73H1600149, 73H1600341, 73H1600902, 73…Lot #'s: 73D1600174, 73D1600587, 73E1600661, 73F1600015, 73G1600729, 73H1600012, 73H1600149, 73H1600341, 73H1600902, 73J1600062, 73L1600025, 73L1600210, 73L1600445, 73M1500036, and 73M1500036 |
|---|
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-3222-2017%22
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