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MEDLINE INDUSTRIES
MEDLINE INDUSTRIES, INC. · Model DYND50230B · UDI-DI 10888277706323
10
510(k) clearances
306
Adverse events
14
Recalls
206
Facilities
Description
CUSTOM,UMD,TUBING,SUCTION,BUBBLE,NS
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | DeRoyal Industries Inc | Due to the inner diameter of the suction tubing connector being smaller than the suction canister lid port connection. This size difference, combined with the durometer of the plas |
| 2017-10-24 | Medtronic Minimally Invasive Therapies Group | Incorrect packaging. In one lot of Argyle Suction Tubing, the pouch may be incorrectly labeled as the Salem Sump Dual Lumen Stomach Tube. This product may have been distributed wit |
| 2016-06-27 | ConMed Corporation | The packaging seal may contain a crease. The crease may result in an open channel. These channels may compromise sterility of the product. |
| 2010-08-16 | Cardinal Health | The packaging seals may not be intact, resulting in compromised sterility for the listed Medi-Vac Non-Conductive Tubing. |
| 2010-08-16 | Cardinal Health | The packaging seals may not be intact, resulting in compromised sterility for the listed Medi-Vac Non-Conductive Tubing. |
| 2010-08-16 | Cardinal Health | The packaging seals may not be intact, resulting in compromised sterility for the listed Medi-Vac Non-Conductive Tubing. |
| 2010-08-16 | Cardinal Health | The packaging seals may not be intact, resulting in compromised sterility for the listed Medi-Vac Non-Conductive Tubing. |
| 2010-08-16 | Cardinal Health | The packaging seals may not be intact, resulting in compromised sterility for the listed Medi-Vac Non-Conductive Tubing. |
| 2010-08-16 | Cardinal Health | The packaging seals may not be intact, resulting in compromised sterility for the listed Medi-Vac Non-Conductive Tubing. |
| 2010-08-16 | Cardinal Health | The packaging seals may not be intact, resulting in compromised sterility for the listed Medi-Vac Non-Conductive Tubing. |
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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.