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Typenex Wound Drainage

TYPENEX MEDICAL LLC · Model WD0703TK5 · UDI-DI 00812269031349

KGZ
10
510(k) clearances
890
Adverse events (10 deaths)
23
Recalls
213
Facilities

Description

Kit with 400 ml Spring Reservoir and 15 FR Perforated Round, with Trocar

Recalls

DateFirmReason
2025-10-29B Braun Medical IncPotential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
2025-10-29B Braun Medical IncPotential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
2025-10-29B Braun Medical IncPotential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
2025-03-27Galt Medical CorporationDue to a potential open seal in the sterile barrier packaging .
2020-11-16Galt Medical CorporationDue to a manufacturing issue, the catheter tip geometry is incorrect (thicker wall) resulting in a more obtuse tip angle.
2019-05-02Cook Inc.The products may have been manufactured without the bottom seal on the outer packaging, compromising the sterility of the product.
2018-05-04Vascular Solutions, Inc.The supplier of Drainer(R) centesis catheters notified Vascular Solutions, Inc. that there is a potential for certain production lots to contain unsafe levels of bacterial endotoxi
2018-05-02Galt Medical CorporationThe products listed might contain unsafe levels of bacterial endotoxins (Pyrogens) that were introduced during a manufacturing step. Bacterial Endotoxins also called pyrogenic bact
2018-05-02Galt Medical CorporationThe products listed might contain unsafe levels of bacterial endotoxins (Pyrogens) that were introduced during a manufacturing step. Bacterial Endotoxins also called pyrogenic bact
2018-05-02Galt Medical CorporationThe products listed might contain unsafe levels of bacterial endotoxins (Pyrogens) that were introduced during a manufacturing step. Bacterial Endotoxins also called pyrogenic bact

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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.