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Henry Schein Inc.

Henry Schein Inc.: 2 recalls posted by FDA since August 2026.

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All recalls (2)

Henry Schein Perma Sharp Surgical Sutures

Perma Sharp Sutures lack 510(k) clearance.

Moderate risk, FDA, , Unapproved product

Henry Schein Structur 2 SC and Grandio Restorative Materials

Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.

Moderate risk, FDA, , Device defect
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