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HomeTRICOR SYSTEMS, INC. › Dri-Scope Aid - Cabinet - Cetacea "F" Port Tubings, 18 in (5 pack)

Dri-Scope Aid - Cabinet - Cetacea "F" Port Tubings, 18 in (5 pack)

TRICOR SYSTEMS, INC. · Model DS-335-18-5 · UDI-DI 00810053600870

MNL
4
510(k) clearances
664
Adverse events
24
Recalls
234
Facilities

Description

Dri-Scope Aid Cabinet (or TRACKER); 12-month Port Tubing Set; Type Cetecea F 18"; 5 pack The Dri-Scope Aid (DSA) 12-month Port Tubing Set (5 pack) contains (qty 5) 18 inch long port tubings. These connect to the output air ports located on each of the DSA Cabinet (or TRACKER) manifolds. Type F tubings are intended to support Fujifilm endoscopes. Consult TRICOR Systems Inc to determine what DSA Cabinet maintenance items are required to support your system and maintain compliance.

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.