device recall
saveICU Medical, Inc. device recall (Cls II)
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Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000 — Reason: Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silicone seal which may bulge at the top, separate from the body, tear; may result in fluid leaks, occluded fluid flow, inability to inject/withdraw blood product, delayed/interrupted therapy, exposure to biological contaminants, air infused into the body — Status: Ongoing
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same company · ±60 days · 6
- device recallICU Medical Inc. device recall (Cls II)Dec 19, 2025
- device recallICU Medical Inc. device recall (Cls II)Dec 19, 2025
- device recallICU Medical, Inc. device recall (Cls II)Dec 15, 2025
- device recallICU Medical, Inc. device recall (Cls II)Dec 15, 2025
- device recallICU Medical, Inc. device recall (Cls II)Dec 15, 2025
- device recallICU Medical, Inc. device recall (Cls II)Dec 15, 2025
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