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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-1180-06 - Theratron 1000 Cobalt Radiotherapy 2 06/27/2006 MDS Canada Inc. DBA MDS Nordion
Z-1181-06 - Theratron 1000E Cobalt Radiotherapy 2 06/27/2006 MDS Canada Inc. DBA MDS Nordion
Z-1178-06 - Theratron 780C Cobalt Radiotherapy 2 06/27/2006 MDS Canada Inc. DBA MDS Nordion
Z-1179-06 - Theratron 780E Cobalt Radiotherapy 2 06/27/2006 MDS Canada Inc. DBA MDS Nordion
Z-1184-06 - Theratron Elite 100 Cobalt Radiotherapy 2 06/27/2006 MDS Canada Inc. DBA MDS Nordion
Z-1183-06 - Theratron Elite 80 Cobalt Radiotherapy 2 06/27/2006 MDS Canada Inc. DBA MDS Nordion
Z-1182-06 - Theratron Phoenix Cobalt Radiotherapy 2 06/27/2006 MDS Canada Inc. DBA MDS Nordion
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