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ATRAMAT

Internacional Farmacéutica, S.A. de C.V. · Model PGC25 · UDI-DI 07500142057731

GAM
1
510(k) clearances
57,611
Adverse events (88 deaths)
135
Recalls
145
Facilities

Description

ATRAMAT PGC25 SURGICAL SUTURE UNDYED USP 6-0 EP 0.7, 45 CM NEEDLE HPE-11 ATRAGLIDE CUTTING 11 MM 3/8 CIRCLE PGC25 INCOLORO USP 6-0, 45 CM AGUJA HPE-11 CORTANTE ATRAGLIDE 11 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
2024-09-25Ethicon, Inc.Complaints were received regarding needle pull-off and suture degradation. Analysis on returned product from this lot confirmed that some sutures were visually degraded in the pack
2024-05-10Ethicon, Inc.Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection .
2024-05-10Ethicon, Inc.Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection .

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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.