Syneture

Covidien LP · Model US1716 · UDI-DI 10884521592964

OVN Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Custom Suture Pack, (2) 88863090-71, (3) 88863157-51, (3) 88863256-51, (4)88863271-31, (1) 88864705-01V, (1) 88864719-21V, (1) 88864750-31V, (1) 88864750-41V, (2) 88866269-61, (1) 88866618-51, (2) CN-792, (1) S-317, (3) VP-703-X, (3) VP-900-X, (1) VS-845

Recalls

Date	Firm	Reason
2026-03-09	LSL Healthcare Inc.	Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
2025-12-12	Medline Industries, LP	Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the via
2024-04-08	MEDLINE INDUSTRIES, LP - Northfield	Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma
2014-06-12	Medical Action Industries Inc	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12	Medical Action Industries Inc	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12	Medical Action Industries Inc	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12	Medical Action Industries Inc	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12	Medical Action Industries Inc	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12	Medical Action Industries Inc	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12	Medical Action Industries Inc	Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.