Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K931175 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Replacement balloons for use with Sandhill Anorectal Manometry Probes. There is no labeling other t... | 2 | 01/06/2006 |
FEI # 2023374 Sandhill Scientific, Inc |
| Schuster Anorectal Manometry Probe. Labeling applied to the ballon pouch reads in part: ''SANDHILL ... | 2 | 01/06/2006 |
FEI # 2023374 Sandhill Scientific, Inc |
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