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Lapcap2

LIFE CARE MEDICAL DEVICES LIMITED · Model LC2-STD · UDI-DI 05060484670002

HIF Prescription

510(k) clearances

7,497

Adverse events (34 deaths)

Recalls

140

Facilities

Description

A sterile, singe use, acrylic dome shaped device with a port for attachment of the suction system and septum for the insertion of a Veress needle. It assists in the blind passage of a 14G Veress needle to establish a pneumoperitoneum prior to laparoscopic procedures. The device is centered over the umbilicus, a suction hose is attached to the suction port and negative pressure applied. The abdomen rises, allowing the Veress needle to be inserted into the created space. Inert gas is delivered to replace the negative pressure.

Recalls

Date	Firm	Reason
2026-06-16	Olympus Corporation of the Americas	Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
2026-05-14	ConMed Corporation	Potential for overpressure alerts.
2026-05-14	ConMed Corporation	Potential for overpressure alerts.
2026-05-14	ConMed Corporation	Potential for overpressure alerts.
2026-05-14	ConMed Corporation	Potential for overpressure alerts.
2026-05-14	ConMed Corporation	Potential for overpressure alerts.
2026-05-14	ConMed Corporation	Potential for overpressure alerts.
2026-05-14	ConMed Corporation	Potential for overpressure alerts.
2026-05-14	ConMed Corporation	Potential for overpressure alerts.
2026-05-14	ConMed Corporation	Potential for overpressure alerts.

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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.