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INTEGRA®

PMT CORPORATION · Model 3612ES-16L-I · UDI-DI 00650551003434

LCJ Prescription

510(k) clearances

5,147

Adverse events (4 deaths)

Recalls

Facilities

Description

INTEGRA TE, CRESCENT, ENHANCED SURFACE, BREAST, INTERNAL PORT 500CC, 11.3X16CM, 6.3CM PROJECTION

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.