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Alleset

GRI Medical & Electronic Technology Co., Ltd. · Model 37-2120-S · UDI-DI 16931918181523

HIF

510(k) clearances

7,600

Adverse events (34 deaths)

Recalls

140

Facilities

Description

Veress Needle_120mm_Sterile_72ea/cs

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.