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Premilene

B BRAUN SURGICAL SA · Model X2090906 · UDI-DI 04046963698720

GAW Prescription
10
510(k) clearances
19,686
Adverse events (226 deaths)
28
Recalls
110
Facilities

Description

PREMILENE 5/0 (1) 75CM 2XHR26 CV RCP

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
2024-12-20Ethicon, 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
2022-12-02Covidien, LPSterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
2022-12-02Covidien, LPSterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
2018-05-07Ethicon, Inc.The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to caus
2018-05-07Ethicon, Inc.The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to caus
2018-05-07Ethicon, Inc.The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to caus

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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.