Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K991932 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 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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