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Syneture
Covidien LP · Model US1755 · UDI-DI 10884521795488
OVN
Prescription
0
510(k) clearances
40
Adverse events
10
Recalls
34
Facilities
Description
Custom Suture Pack, (1) VP702MX, (1) VP902MX, (1) VP557MX, (3) 8886867901, (2) CL964, (1) CL843, (3) SM5637, (5) 8886325151, (2) GS62M, (1) S317, (1) S193, (1) S195, (1) GLS322, (1) 8886327131
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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Get your free API keyRead the docsData 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.