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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 17 of 17 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0950-2019 - AF 550 x 8ML/HR 2ML 15LO CPNBMT8015XL CP, Product code MT8015XL CPNB, Arrow AutoFuser Disposable Pain Control Pump 2 02/25/2019 Arrow International Inc
Z-0951-2019 - AF 550x8ML/H 2ML 15LO 8.7" DUAL CATHS, 4, Product code MT8015XLYK10 CP, Arrow AutoFuser Disposable Pain Control Pump 2 02/25/2019 Arrow International Inc
Z-0952-2019 - AF w/AS 550 x 0.5-7 ml,w/Y site,DL CPNB, Product code MVAXL2Y CPNB, Arrow AutoFuser Disposable Pain Control Pump 2 02/25/2019 Arrow International Inc
Z-0953-2019 - AF w/AS 550 x 1-14 ml/hr, 5ml30 LOCPNB, Product code MVBX30XLCPNB, Arrow AutoFuser Disposable Pain Control Pump 2 02/25/2019 Arrow International Inc
Z-0954-2019 - AF w/AS 550 x 1-14ML/HR 2ML-15LO CPNB, Product code MVBT15XL-CPNB, Arrow AutoFuser Disposable Pain Control Pump 2 02/25/2019 Arrow International Inc
Z-0955-2019 - AF w/AS 550 x 1-14ML/HR 2ML-30LO CPNB, Product code MVBT30XL CPNB, Arrow AutoFuser Disposable Pain Control Pump 2 02/25/2019 Arrow International Inc
Z-0941-2019 - AF w/AS 550x 0.5 7 ml/hr, 5ml 30 LO CPNB, Product code MVAX30XL CPNB, Arrow AutoFuser Disposable Pain Control Pump 2 02/25/2019 Arrow International Inc
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