Medical Device Recalls
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21 to 30 of 500 Results
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Class 1 Recall Date from: 01%2F01%2F2020 Recall Date to: 02%2F10%2F2020 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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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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