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Codman & Shurtleff Recalls
59 recalls on record · February 27, 2013 to August 21, 2019 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 9, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls MedStream Refill Kit, U.S: 91-4287 Product Usage: The Medstream programmable pump is intended for the intrathecal de
Hazard: Drug flow rates exceeding programmed flow rates.
October 9, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls MedStream Programmable Pump; 40ml - 91-4201US Usage: The Medstream programmable pump is intended for the intrathecal
Hazard: Drug flow rates exceeding programmed flow rates.
October 9, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls MedStream Programmable Pump; 20ml - 91-4200US Product Usage: The Medstream programmable pump is intended for the int
Hazard: Drug flow rates exceeding programmed flow rates.
July 24, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls MedStream Programmable Infusion Pump , Implantable for the intrathecal delivery of Baclofen or Morphine Product Code:
Hazard: Miscalibrated Fill Level Sensor may affect dosing level
July 24, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery of Baclofen or Morphine Product Code:91-
Hazard: Miscalibrated Fill Level Sensor may affect dosing level
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMC61000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx100 GUIDING CATH HH Product Code: GHH61000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 Intended for use in the coronary, peripheral, and neurovas
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx90 GUIDING CATH HH Product Code: GHH50900000 Intended for use in the coronary, peripheral, and neurovas
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx90 GUIDING CATH ST Product Code: GST60900000 Intended for use in the coronary, peripheral, and neurovas
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000 Intended for use in the coronary, peripheral, and neurovas
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx100 GUIDING CATH ST Product Code: GST51000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx90 GUIDING CATH MPD Product Code: GMD50900000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx90 GUIDING CATH MPC Product Code: GMC50900000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx90 GUIDING CATH MCV Product Code: GCB50900000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx100 GUIDING CATH MC Product Code: GCB51000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx100 GUIDING CATH S2 Product Code: GSM61000000 Intended for use in the coronary, peripheral, and neurov
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx100 GUIDING CATH MC Product Code: GCB61000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx100 GUIDING CATH S2 Product Code: GSM51000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx100 GUIDING CATH MP Product Code:GMD51000000 Intended for use in the coronary, peripheral, and neurovas
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx100 GUIDING CATH MPD Product Code: GMD60900000 Intended for use in the coronary, peripheral, and neurov
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GMC51000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GHH51000000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000 Intended for use in the coronary, peripheral, and neurovas
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx90 GUIDING CATH S2 Product Code: GSM50900000 Intended for use in the coronary, peripheral, and neurovas
Hazard: Sterility of device may be compromised due to lack of package integrity
February 27, 2013Medical DevicesFDA
Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx90 GUIDING CATH MPC Product Code: GMC60900000 Intended for use in the coronary, peripheral, and neurova
Hazard: Sterility of device may be compromised due to lack of packaging integrity