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U.S. Department of Health and Human Services

Medical Device Recalls

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21 to 30 of 500 Results *
Class 1 Recall Date from: 01%2F01%2F2020 Recall Date to: 02%2F10%2F2020
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Product Description
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Recall
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FDA Recall
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Portex 1st Response Adult Manual Resuscitators Ref: 8500P 1 05/22/2003 Sims Portex Inc.
Portex 1st Response Adult Manual Resuscitators Ref: 8503P 1 05/22/2003 Sims Portex Inc.
Portex 1st Response Adult Manual Resuscitators Ref: 8506P 1 05/22/2003 Sims Portex Inc.
ESPRIT VENTILATOR, Model V1000 1 07/01/2003 Respironics California Inc
Becton Dickinson's ProbeTec (tm) ET Instrument 1 08/20/2003 Becton Dickinson & Co.
VIDAS Chlamydia Assay (CHL) for In-Vitro Diagnostic Use Product Number: 30101 1 10/15/2003 bioMerieux
CoaguChek brand PT Test Strips; U.S. catalog number 3116247 (professional use), 3116239 (patient sel... 1 10/15/2003 Roche Diagnostics Corp.
ComfortGel Nasal Mask size small 1 12/10/2003 Respironics, Inc.
ComfortGel Nasal Mask size large 1 12/10/2003 Respironics, Inc.
ComfortGel Nasal Mask size medium 1 12/10/2003 Respironics, Inc.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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