Medical Device Recalls
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1 to 10 of 12 Results
Recall Date to: 04/20/2015 510(K) Number: K980987 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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# 309603 -- Syringe 5Ml LL syringe. | 2 | 07/28/2005 | Becton Dickinson & Company |
# 309604 -- Syringe 10 mL LL | 2 | 07/28/2005 | Becton Dickinson & Company |
#309604 -- 10 mL syringe | 2 | 07/28/2005 | Becton Dickinson & Company |
#309644 -- 10 ml syringe with 20 G1'' Needle | 2 | 07/28/2005 | Becton Dickinson & Company |
#309661 -- Syringe only ll 20 mL | 2 | 07/28/2005 | Becton Dickinson & Company |
BD 30ml Syringe Luer-Lok tip Sterile BD, Franklin Lakes, NJ Made in USA | 2 | 04/05/2007 | Becton Dickinson & Company |
BD 5ml Syringe Luer-Lok Tip Bulk Sterile Convenience Pak Latex Free | 2 | 05/24/2007 | Becton Dickinson & Company |
Bard PEG Safety System ''Guidewire'' Reorder Number: 000930 | 2 | 09/11/2003 | Bard Endoscopic Technologies |
Bard PEG Safety System ''Guidewire'' Reorder Number: 001928 | 2 | 09/11/2003 | Bard Endoscopic Technologies |
Bard Ponsky PEG Safety System ''Pull'' Reoder Number: 001927 | 2 | 09/11/2003 | Bard Endoscopic Technologies |
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