Moderate riskFDA DeviceClass II

Henry Schein silk sutures recalled for lacking 510(k) clearance

Henry Schein Inc. is recalling Perma Sharp silk nonabsorbable surgical sutures because the products lack 510(k) clearance from FDA. The recall covers 140 units distributed in the U.S. and in Canada, Uganda, and the Cayman Islands. No injuries have been reported.

From the FDA notice · Read the official notice ↗

What to do

  1. Set aside any units of model PSN683S (HSI Item No. 600-6411) from lot numbers 0124001HF, 0124002HF, 0125009HF, 0125010HF, 0125026HF, 0125034HF, 0125040HF, or 0125041HF (UDI-DI 10889950001605).
  2. The notice doesn't say how to get a replacement or refund; contact Henry Schein Inc. for next steps.

Is yours affected?

Compare your label or packaging with the recalled product.

Product
Generic Name: Perma Sharp Sutures; Generic Name: Silk Nonabsorbable Surgical Suture; Model/Catalog Number: PSN683S (HSI Item No. 600-6411); Product Description: Sterile, natural, nonabsorbable, braided 4-0 black silk surgical suture, 18-inch length, with C-6 18.7 mm, 3/8-circle reverse-cutting needle. Component: N/A;
Sold in
Nationwide
Made for
All ages (under 100 years)

This recall covers 13 products — see all of them.

Details

Units affected
140
Illnesses reported
None reported
Manufactured in
41 Weaver Rd, Denver, Pennsylvania, United States
Classification
Class II
Recall number
Z-0339-2027

In the FDA's words

Description
Generic Name: Perma Sharp Sutures; Generic Name: Silk Nonabsorbable Surgical Suture; Model/Catalog Number: PSN683S (HSI Item No. 600-6411); Product Description: Sterile, natural, nonabsorbable, braided 4-0 black silk surgical suture, 18-inch length, with C-6 18.7 mm, 3/8-circle reverse-cutting needle. Component: N/A; Products lack 510(k) clearance. Model/Catalog Number: PSN683S (HSI Item No. 600-6411); UDI-DI: 10889950001605; Lot Numbers: 0124001HF, 0124002HF, 0125009HF, 0125010HF, 0125026HF, 0125034HF, 0125040HF, 0125041HF Distribution: Worldwide distribution - U.S. Nationwide and the countries of Canada, Uganda, and the Cayman Islands. Affected quantity: 140
Hazard
Products lack 510(k) clearance.

13 products in this recall

Henry Schein Perma Sharp sutures recalled for lacking 510(k) clearance

Henry Schein is recalling 13 Perma Sharp surgical suture products, sold under Henry Schein and HSI item numbers, because the products lack 510(k) clearance from FDA. The recall covers U.S. nationwide distribution and shipments to Canada, Uganda, and the Cayman Islands. No injuries have been reported.

The agency lists each product separately. Check every one you might have.

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