Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Open, Classified

Stryker Sustainability Solutions REF HARH36 Ethicon Endo-Surgery, Inc. Harmonic ACE +7, Shears with Advanced Hemostasis 5mm Diameter x 36cm - Product Usage: indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired. The instruments can be used as an adjunct to or substitute for electrosurgery, lasers and steel scalpels in general, plastic, pediatric, gynecologic, urologic, thoracic, exposure to orthopedic structures (such as spine and joint space), sealing and transection of lymphatic vessels, and other open and endoscopic procedures.

FDA Recall Z-1327-2021 · Posted None

Recall StatusOpen, Classified
Product CodeNLQ
Date Initiated2021-01-19
Product Quantity102 units

Reason for Recall

Product was distributed without receiving regulatory clearance.

Firm Action

On 01/19/2021, the firm sent an "URGENT; MEDICAL DEVICE RECALL" Notification letter its customers informing them that the affected products are currently under evaluation and do not have Regulatory Clearance and the safety and efficacy of the product has not been assessed. Customers are instructed to: 1. Discontinue use of the affected products. 2. Check their inventory for the affected products. 3. Complete the Urgent Medical Device Recall Business Reply Form and indicate if any of the affected product remains in their inventory. They are instructed to return the completed form through on of the following methods: a) Email: [email protected] b. To their Recalling Firm's Sales Representative c. Fax: 480-763-5345 The form must be completed and returned to the Recalling Firm even if no affected product is found. 4. If any of the affected products have been forwarded to additional facilities, please contact these facilities and communicate this recall to them. 5. Maintain awareness of this communication internally until all required actions have been completed with their facility. If the returned Urgent Medical Device Business Reply Forms indicated that any affected products remains in customer's inventory, a Recalling Firm Representative will contact them to arrange for the removal of the product(s). Any questions regarding this Recall - contact Post Market Surveillance Manager at 888-888-3433 or email [email protected]

Root Cause

Device Design

Distribution Pattern

Worldwide distribution - U.S. Nationwide distribution in the state of OH and the country of Israel.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑