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Integra

PMT CORPORATION · Model 3612-15IR-ST · UDI-DI 00650551002291

LCJ Prescription

510(k) clearances

5,172

Adverse events (4 deaths)

Recalls

Facilities

Description

Integra TE, BREAST, TEARDROP, SMOOTH, SINGLE STAGE, INTERNAL RESEAL PORT, SUTURE TABS, 12x16cm, 700cc FILL, 8.5 PROJ. CM

Recalls

Date	Firm	Reason
2026-02-18	Mentor Texas, LP.	Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18	Mentor Texas, LP.	Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18	Mentor Texas, LP.	Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18	Mentor Texas, LP.	Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18	Mentor Texas, LP.	Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18	Mentor Texas, LP.	Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-18	Mentor Texas, LP.	Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
2026-02-02	B Braun Medical Inc	The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
2026-02-02	B Braun Medical Inc	The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
2026-02-02	B Braun Medical Inc	The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

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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.