Home › TRICOR SYSTEMS, INC. › Dri-Scope Aid - Connectors Kit -Type O-EBUS (1 pack)
Dri-Scope Aid - Connectors Kit -Type O-EBUS (1 pack)
TRICOR SYSTEMS, INC. · Model 401789-321 · UDI-DI 00810053600733
4
510(k) clearances
664
Adverse events
24
Recalls
234
Facilities
Description
Dri-Scope Aid; Single-Use Connectors Kit; Type O-EBUS; 1 pack; The Dri-Scope Aid single-use Connectors Kit pack contains 3 single-use connectors that are used to attach to various endoscope ports for drying. Type O-EBUS connectors are intended to primarily support Olympus EBUS endoscopes. Consult TRICOR Systems Inc to determine what Dri-Scope Aid disposables are required to support your endoscope. [REORDER #: 401789-421 (100 pack)]
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-02 | Healthmark 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 |
| 2025-05-02 | Healthmark 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 |
| 2024-01-09 | Mckesson Medical-Surgical Inc. Corporate Office | Facility 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 |
| 2022-05-25 | Mckesson Medical-Surgical Inc. Corporate Office | Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 0 |
| 2022-04-21 | MEDLINE INDUSTRIES, LP - Northfield | Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination. |
| 2022-04-21 | MEDLINE INDUSTRIES, LP - Northfield | Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination. |
| 2022-04-21 | MEDLINE INDUSTRIES, LP - Northfield | Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination. |
| 2022-04-21 | MEDLINE INDUSTRIES, LP - Northfield | Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination. |
| 2022-04-21 | MEDLINE INDUSTRIES, LP - Northfield | Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination. |
| 2020-07-09 | Medline Industries Inc | Potential risk of brush detachment during cleaning. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.