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MPM Medical Supply (Private Label)

MANAN MEDICAL PRODUCTS, INC. · Model TNL0815 · UDI-DI 00859013006093

DWO Prescription
1
510(k) clearances
103
Adverse events
9
Recalls
45
Facilities

Description

8GA X 15 CM (Target Needle-Locking)

Recalls

DateFirmReason
2021-08-05M.D.L. S.r.l.Sterility assurance may be compromised.
2018-12-18Angiotech (Manan Medical Products, Inc.)Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
2018-12-18Angiotech (Manan Medical Products, Inc.)Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
2018-12-18Angiotech (Manan Medical Products, Inc.)Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
2018-12-18Angiotech (Manan Medical Products, Inc.)Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
2018-12-18Angiotech (Manan Medical Products, Inc.)Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
2018-12-18Angiotech (Manan Medical Products, Inc.)Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
2018-12-18Angiotech (Manan Medical Products, Inc.)Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
2015-06-15Mermaid Medical A/SMermaid Medical A/S is recalling some of their M-Biopsy Coaxial Introducer Needles because of the potential for small plastic pieces to be present in the luer of the cannula.

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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.