Home › M.D.L. S.R.L. › Intro
Intro
M.D.L. S.R.L. · Model PT17044 · UDI-DI 08056138586536
MJG
Prescription
7
510(k) clearances
44
Adverse events
4
Recalls
67
Facilities
Description
COAXIAL INTRODUCER NEEDLE 17G X 44 mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma |
| 2024-03-01 | Cook Incorporated | Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility |
| 2021-08-05 | M.D.L. S.r.l. | Sterility assurance may be compromised. |
| 2010-07-02 | Medical Device Technologies, Inc. | Medical Device Technologies, Inc., dba Angiotech, Gaineville, Florida is recalling Tru-Core II Disposable Biopsy Devices due to compromised packaging integrity. The Tru-Core Di |
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.
