Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K021567 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Arrow International StimuCath(R) Continuous Nerve Block Kit, ASK-19608-SFH, Lot # MF0127039 Permi... | 2 | 11/30/2011 |
FEI # 3015859709 Arrow International Inc |
| Arrow Continuous Nerve Block Needle, Latex-Free* Rx only*Sterile*Arrow International Inc., 2400 Bern... | 2 | 06/01/2005 |
FEI # 3015859709 Arrow International Inc |
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