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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 54 Results
510(K) Number: K983559
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Product Description
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FDA Recall
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120" (305cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, 3 Clave®, Rotating Luer, 2 Ext, Steril... 2 08/07/2018 ICU Medical, Inc.
121" (307 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, 3 Clave®, Remv 4-Way Stopcock, T-Conn... 2 08/07/2018 ICU Medical, Inc.
132" (335 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, Clave®, 4-Way Stopcock, Rotating Luer... 2 08/07/2018 ICU Medical, Inc.
175" (445 cm) Y-Type Blood Set w/170 Micron Blood Filter, Hand Pump, Inj Site, Remv 3 Gang 4-Way Sto... 2 08/07/2018 ICU Medical, Inc.
140" (356 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, 3 Clave®, Remv 4-Way Stopcock, Rotati... 2 08/07/2018 ICU Medical, Inc.
100" (254 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter, Hand Pump, 2 Clave®, Rotating Luer w/Fil... 2 08/07/2018 ICU Medical, Inc.
125" (318 cm) Bifuse Blood Set w/170 Micron Filter, Hand Pump, 4 MicroClave® Clear, Rotating Luer, 1... 2 08/07/2018 ICU Medical, Inc.
164" (417 cm) 20 Drop Y-Type Blood Admin Set w/200 Micron Filter, Hand Pump, Remv 4 Gang 4-Way Stopc... 2 08/07/2018 ICU Medical, Inc.
105" (267 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, Pre-Slit Port, MicroClave® Clear, Rot... 2 08/07/2018 ICU Medical, Inc.
94" (239 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, MicroClave® Clear, Rotating Luer, Appr... 2 08/07/2018 ICU Medical, Inc.
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