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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 500 Results *
Recall Date from: 01/01/2016 Recall Date to: 06/13/2016
 
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The Vesa 75/100 adaptation with rotation is an accessory to a surgical camera intended to be used to... 2 07/09/2019 Richard Wolf Medical Instruments Corp.
CareLink iPro2 Reports, Model No. MMT-7340 is software intended to retrospectively calibrates senso... 2 10/11/2018 Medtronic MiniMed Inc.
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... 2 10/11/2018 Synthes (USA) Products LLC
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... 2 10/11/2018 Synthes (USA) Products LLC
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... 2 10/11/2018 Synthes (USA) Products LLC
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... 2 10/11/2018 Synthes (USA) Products LLC
RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver 2 10/11/2018 RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... 2 10/11/2018 Synthes (USA) Products LLC
31" (79 cm) Appx. 3.4 ml, 20 Drop Admin Set w/ Integrated ChemoLock Port Drip Chamber, Spiros, Bag H... 2 10/11/2018 ICU Medical, Inc.
Access 2 Immunoassay System, Remanufactured, Catalog No. 386220 is an invitro diagnostic device used... 2 10/11/2018 Beckman Coulter Inc.

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