Home › Medical Components, Inc. › TRIPLE LUMEN INFUSION CATHETERSTRIPLE LUMEN INFUSION CATHETERS
TRIPLE LUMEN INFUSION CATHETERSTRIPLE LUMEN INFUSION CATHETERS
Medical Components, Inc. · Model MC3L-8S-PA · UDI-DI 00884908097009
JCY
Prescription
10
510(k) clearances
35
Adverse events (6 deaths)
3
Recalls
37
Facilities
Description
7F X 20CM TRIPLE LUMEN7F X 20CM INFUSION CATHETER TRAYINFUSION C
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-08-31 | DePuy Mitek, Inc., a Johnson & Johnson Co. | Leakage of FMS gravity tub sets (281113) at the bulb and tube connection |
| 2010-09-10 | Linvatec Corp. dba ConMed Linvatec | On 09/13/2010 ConMed Linvatec, Largo, FL initiated a recall on 24k100 Arthroscopy Outflow/Suction Tube Set used with the ConMed Linvatec 24k Pump. The 24k100 Arthroscopy Outflow/S |
| 2009-09-01 | Medical Device Technologies, Inc. | Medical Device Technologies doing business as Angiotech has conducted a recall on Angiotech Breast Localization Needles, Soft Tissue Biopsy Needles, Vascular Access Needles, Bone B |
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.