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ATRAMAT
Internacional Farmacéutica, S.A. de C.V. · Model PGLA90 · UDI-DI 07500142046797
1
510(k) clearances
57,611
Adverse events (88 deaths)
135
Recalls
145
Facilities
Description
ATRAMAT PGLA90 SURGICAL SUTURE VIOLET USP 0 EP 3,5, 70 CM NEEDLE SG-36 PREMIUM HEAVY TAPER POINT 36 MM 1/2 CIRCLE PGLA90 VIOLETA USP 0, 70 CM AGUJA SG-36 AHUSADA GRUESA PREMIUM 36 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 |
| 2024-09-25 | Ethicon, 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 |
| 2024-05-10 | Ethicon, Inc. | Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection . |
| 2024-05-10 | Ethicon, 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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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.