Home › Internacional Farmacéutica, S.A. de C.V. › ATRAMAT
ATRAMAT
Internacional Farmacéutica, S.A. de C.V. · Model POLIPROPILENO · UDI-DI 07500142001949
1
510(k) clearances
20,303
Adverse events (226 deaths)
33
Recalls
112
Facilities
Description
ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 0 EP 3,5, 75 CM NEEDLE R-26 REGULAR TAPER POINT 26 MM 1/2 CIRCLE POLIPROPILENO AZUL USP 0, 75 CM AGUJA R-26 AHUSADA REGULAR 26 MM 1/2 CIRCULO
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-09-17 | Henry Schein Inc. | Products lack 510(k) clearance. |
| 2026-06-24 | Covidien, LP | Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v |
| 2026-06-24 | Covidien, LP | Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of v |
| 2024-12-20 | Ethicon, LLC | Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could intr |
| 2024-12-20 | Ethicon, LLC | Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could intr |
| 2024-12-20 | Ethicon, LLC | Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could intr |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
