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HomeSurgical Specialties México, S. de R.L. de C.V. › Ds18 3-0 Und Pga-Fa 18"/45cm

Ds18 3-0 Und Pga-Fa 18"/45cm

Surgical Specialties México, S. de R.L. de C.V. · Model MC-493N · UDI-DI 00848782017751

GAM Prescription
10
510(k) clearances
56,265
Adverse events (88 deaths)
130
Recalls
144
Facilities

Description

Ds18 3-0 Und Pga-Fa 18"/45cm

Recalls

DateFirmReason
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 .
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 .
2024-03-26SURGICAL SPECIALTIESComplaints have been received with allegations of Incorrect Needle Curvature.
2024-03-08Ethicon, Inc.Degraded and unusable upon removal from the foil pouch due to exposed environmental conditions during transit and storage, compromising sterility
2022-09-28Covidien, LPMedtronic has received 210 reports of needles breaking during endoscopic suturing. The potential harm(s) include a delay in treatment/therapy, the potential for a portion of the ne

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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.