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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-1120-2020 - Prometra Programmable 20mL Pump. Catalog No. 11827 The device is an implantable infusion pump. GTIN-14 00810335020082
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2
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02/10/2020
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FEI # 3010079947 Flowonix Medical Inc
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Z-1121-2020 - Prometra II 20mL Pump. Catalog No. 13827 The device is an implantable infusion pump. GTIN-14 00810335020228
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2
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02/10/2020
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FEI # 3010079947 Flowonix Medical Inc
|
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Z-1125-2020 - Prometra II Programmable 20mL Pump. Catalog No. 93827 The device is an implantable infusion pump. GTIN-14 00810335020YYY (YYY= in-country language specific)
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2
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02/10/2020
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FEI # 3010079947 Flowonix Medical Inc
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Z-1123-2020 - US Clinical 20mL Programmable Pump. Catalog No. 01827 The device is an implantable infusion pump. GTIN-14 00810335020082
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2
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02/10/2020
|
FEI # 3010079947 Flowonix Medical Inc
|
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Z-1124-2020 - Prometra Programmable 20mL Pump. Catalog No. 91827 The device is an implantable infusion pump. GTIN-14 00810335020XXX (XXX = in-country language specific)
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2
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02/10/2020
|
FEI # 3010079947 Flowonix Medical Inc
|
|
Z-1122-2020 - Prometra II 40mL Pump. Catalog No. 16827 The device is an implantable infusion pump. GTIN-14 00810335020242
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2
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02/10/2020
|
FEI # 3010079947 Flowonix Medical Inc
|