Data Foundry

Medical device recalls 2017

Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm… — Class II medical device recall Z-3224-2017

Terminated recall by Teleflex Medical, reported 2017-10-04, distributed in AL, AZ, CA, FL, GA, IA, IL, IN…. For some of the recalled products, the security of the connection between the shaft and the tool tip may be co

Recall numberZ-3224-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTeleflex Medical, Morrisville, NC, United States
Recall initiated2017-07-19
Classified2017-09-27
Reported by FDA2017-10-04
Terminated2020-10-06
DistributedAL, 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
Countries outside the USAE, AU, BE, CH, CN, CZ, DE, ES, FI, FR, GB, HK, IE, IL, IR, IT, JP, KR, NL, NO, QA, RO, SA, SG, TR, TW, ZA
Quantity20,039 total
Lot numbers73B1600168, 73B1700525, 73C1600057, 73C1600152, 73C1600267, 73C1600327, 73D1600176, 73D1600481, 73E1600001, 73E1600662, 73F1600520, 73F1600594, 73F1600697, 73G1600015, 73G1600177, 73G1600178, 73G1600557, 73G1600730, 73H1600567, 73J1600182, 73M1600025, 73M1600026, 73M1600232, 73M1600233, 73M1600328

Product

Percuvance 29cm Shaft 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 recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3224-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.