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ATRAMAT

Internacional Farmacéutica, S.A. de C.V. · Model POLIPROPILENO · UDI-DI 07500142080067

GAW
1
510(k) clearances
20,303
Adverse events (226 deaths)
33
Recalls
112
Facilities

Description

ATRAMAT POLYPROPYLENE SURGICAL SUTURE BLUE USP 8-0 EP 0,4, 60 CM DOUBLE NEEDLE CVSE-8 CARDIOVASCULAR PREMIUM TAPER POINT 8 MM 3/8 CIRCLE POLIPROPILENO AZUL USP 8-0, 60 CM DOBLE AGUJA CVSE-8 CARDIOVASCULAR AHUSADA PREMIUM 8 MM 3/8 CIRCULO

Recalls

DateFirmReason
2026-09-17Henry Schein Inc.Products lack 510(k) clearance.
2026-09-17Henry Schein Inc.Products lack 510(k) clearance.
2026-09-17Henry Schein Inc.Products lack 510(k) clearance.
2026-09-17Henry Schein Inc.Products lack 510(k) clearance.
2026-09-17Henry Schein Inc.Products lack 510(k) clearance.
2026-06-24Covidien, LPProduct 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
2026-06-24Covidien, LPProduct 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
2024-12-20Ethicon, LLCSutures 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
2024-12-20Ethicon, LLCSutures 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
2024-12-20Ethicon, LLCSutures 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

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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.