Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K915571 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Vented and Non-Vented Burette I.V. Gravity Feed Administration Sets; sterile, Rx, single use devices... | 2 | 06/27/2003 | Abbott Laboratories HPD/ADD |
I.V. Extension Sets; sterile, Rx, single use devices; Abbott Laboratories, North Chicago, IL 60064 U... | 2 | 06/27/2003 | Abbott Laboratories HPD/ADD |
LifeShield Latex-Free 150 mL Burette Set, Nonvented, 117 Inch with Prepierced Injection Site, Backch... | 3 | 06/05/2003 | Abbott Laboratories HPD/ADD |
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