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-0164-2020 - Rifton TRAM Standard Base, SKU K310, powered lift device | 2 | 10/22/2019 |
FEI # 1319061 Community Products, LLC |
| Z-0166-2020 - Rifton E-Pacer, SKU K660, powered lift device | 2 | 10/22/2019 |
FEI # 1319061 Community Products, LLC |
| Z-0165-2020 - Rifton TRAM Low Base, SKU K320, powered lift device | 2 | 10/22/2019 |
FEI # 1319061 Community Products, LLC |
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