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Dri-Scope Aid - Connectors Kits - Type F2 (100 pack)

TRICOR SYSTEMS, INC. · Model 401789-420 · UDI-DI 00810053600702

MNL
4
510(k) clearances
674
Adverse events
24
Recalls
234
Facilities

Description

Dri-Scope Aid; Single-Use Connectors Kits; Type F2; 100 pack; 1 box; The Dri-Scope Aid single-use Connectors Kit box contains 100 kit packs. Each individual pack contains 3 single-use connectors that are used to attach to various endoscope ports for drying. Type F2 connectors are intended to primarily support Fujifilm type endoscopes. Consult TRICOR Systems Inc to determine what Dri-Scope Aid disposables are required to support your endoscope.

Recalls

DateFirmReason
2025-05-02Healthmark Industries Co., Inc.During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their inve
2025-05-02Healthmark Industries Co., Inc.During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their inve
2024-01-09Mckesson Medical-Surgical Inc. Corporate OfficeFacility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 De
2022-05-25Mckesson Medical-Surgical Inc. Corporate OfficeFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 0
2022-04-21MEDLINE INDUSTRIES, LP - NorthfieldSporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
2022-04-21MEDLINE INDUSTRIES, LP - NorthfieldSporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
2022-04-21MEDLINE INDUSTRIES, LP - NorthfieldSporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
2022-04-21MEDLINE INDUSTRIES, LP - NorthfieldSporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
2022-04-21MEDLINE INDUSTRIES, LP - NorthfieldSporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
2020-07-09Medline Industries IncPotential risk of brush detachment during cleaning.

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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.