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Endo Carry-On Procedure Kit

MEDIVATORS INC. · Model CPK-106929-0001 · UDI-DI 00677964080296

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

Description

Endo Carry-On Procedure Kit

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.