Moderate riskFDA DeviceClass II

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

Henry Schein Inc. is recalling Perma Sharp silk surgical sutures, model PSN7772S, because the products lack 510(k) clearance from FDA. The notice reports no injuries. About 33 units were distributed in the U.S. and in Canada, Uganda, and the Cayman Islands.

From the FDA notice · Read the official notice ↗

What to do

  1. Set aside any units from the affected lots so they are not used on patients.
  2. Check for model PSN7772S (HSI Item No. 600-3090), UDI-DI 10889950001810, and lot numbers 0125005HF or 0125028HF.
  3. The notice doesn't say how to get a refund or replacement; contact Henry Schein Inc. or your supplier 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: PSN7772S (HSI Item No. 600-3090); Product Description: Sterile, natural, nonabsorbable, braided 3-0 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 (0 months and older)

This recall covers 13 products — see all of them.

Details

Units affected
33
Illnesses reported
None reported
Manufactured in
41 Weaver Rd, Denver, Pennsylvania, United States
Classification
Class II
Recall number
Z-0336-2027

In the FDA's words

Description
Generic Name: Perma Sharp Sutures; Generic Name: Silk Nonabsorbable Surgical Suture; Model/Catalog Number: PSN7772S (HSI Item No. 600-3090); Product Description: Sterile, natural, nonabsorbable, braided 3-0 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: PSN7772S (HSI Item No. 600-3090); UDI-DI: 10889950001810; Lot Numbers: 0125005HF, 0125028HF; Distribution: Worldwide distribution - U.S. Nationwide and the countries of Canada, Uganda, and the Cayman Islands. Affected quantity: 33
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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