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Access Scientific Recalls
14 recalls on record · September 25, 2013 to July 22, 2020 · Medical Devices
Recalls by year
13
20
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 22, 2020Medical DevicesFDA
Access Scientific LLC recalls POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Extended Dwell Catheter made of ChronoFlex C with BioGUARD
Hazard: Convenience kit mislabeled with the incorrect catheter effective length on the device label and the packaging label. Use may lead to a delay or interruption of treatment and user dissatisfaction or annoyance.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 8cm Max Barrier Kit. REF/UDI / 94116/10859821006237
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 10cm Quick Kit. REF/UDI / 94115/10859821006251 - Pro
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 3Fr 6cm Pediatric Kit. REF/UDI / 94124/10859821006480 -
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 3Fr 6cm Quick Kit. REF/UDI / 94123/10859821006473 - Prod
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 10cm Extended Dwell Catheter. REF/UDI / 94108/008598
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 8cm Quick Kit. REF/UDI / 94114/10859821006220 - Prod
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 10cm Max Barrier Kit. REF/UDI / 94107/10859821006206
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 8cm Max Barrier Kit. REF/UDI / 94106/10859821006176
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 10cm Quick Kit. REF/UDI / 94105/10859821006190 - Pro
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 8cm Quick Kit. REF/UDI / 94104/10859821006169 - Prod
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND"XL Alternate Site Kit, 4Fr . REF/UDI 80701/10859821006213 -
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
May 20, 2020Medical DevicesFDA
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND" ED Quick Kit 3FR 6cm. REF/UDI 72627/ 00859821006674 - Prod
Hazard: Saline Flush Syringe compromised sterility due to holes in the packaging.
September 25, 2013Medical DevicesFDA
Access Scientific Inc recalls POWERWAND Safety Introducer with Extended Dwell Catheter; Catalog no. 92006. Used to gain access to the vascular sys
Hazard: Access Scientific is recalling the POWERWAND Saftey Introducer with Extended Dwell Catheter because it is mislabeled.