Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Z-1159-06 - Medtronic Zinetics Manometric Catheter, Model 9012P2271. Water perfused, motility catheter. Distributed by Medtronic, Inc. 710 Medtronic Parkway NE, Minneapolis, MN 55432-5604 USA. | 3 | 06/22/2006 |
FEI # 1000135098 Medtronic Gastroenterology / Urology |
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