Latest recalls — page 40
Older notices, newest first.
-
Class II · 2 months ago
Spectral Instruments Inc Lago X recall: Momentary absence of On-Screen "X-Ray On" banner during run readiness check
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
-
Class I · 2 months ago
Boston Scientific Enroute Transcarotid Neuroprotection System Plus recall: Potential for arterial sheath tip separation or partial tip separation during
Potential for arterial sheath tip separation or partial tip separation during use.
-
Class III · 2 months ago
Paragon 28, Inc. Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev recall: Device was recalled due to an elevated oxygen level in excess
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material…
-
Class II · 2 months ago
Siemens Healthineers Immulite 2000 Systems SYP recall: Syphilis Screen assay may contain a negative patient bias resulting in low
Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.
-
Class II · 2 months ago
ConvaTec, Inc Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703 recall: Urostomy Pouches may leak from cap during use
Urostomy Pouches may leak from cap during use.
-
Class II · 2 months ago
Philips North America Llc Cardiac Workstation 7000. Product Number: 860441 recall: Device will intermittently provide inaccurate data related to native heart
Device will intermittently provide inaccurate data related to native heart rate.
-
Class I · 2 months ago
BMC/Reacthealth Luna G3 Apap REF LG 3600 recall: Retroactive reporting for 2024 rework conducted at the 3B/React Health
Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse
-
Class II · 2 months ago
Covidien, LLC EndoFlip System that includes: Endoflip 1 System EF-100 05391530810050 recall: The system's 24-hour usage limit results in catheters incorrectly flagged
The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.
-
Class III · 2 months ago
Paragon 28, Inc. Custom Made Device Implant 6123 Navicular Cage Small Right Rev recall: Device was recalled due to an elevated oxygen level in excess
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material…
-
Class II · 2 months ago
Boston Scientific Corporation Suture Cinch Long 1pk. Endoscopic tissue approximation recall: Device may fail to deploy the cinch implant and/or fail to cut the suture
Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.
-
Class II · 2 months ago
Siemens Healthineers Immulite 2000 Systems SYP recall: Syphilis Screen assay may contain a negative patient bias resulting in low
Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.
-
Class II · 2 months ago
Philips North America Llc Cardiac Workstation 5000. Product Number: 860439 recall: Device will intermittently provide inaccurate data related to native heart
Device will intermittently provide inaccurate data related to native heart rate.
-
Class II · 2 months ago
Medtronic MiniMed, Inc. MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW recall: Loaner insulin pumps may have been cleaned with chemically incompatible
Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress…
-
Class II · 2 months ago
American Contract Systems medical procedure kits and trays labeled recall: The recall notice was initiated due to a Medicom Urgent Medical Device
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges…
-
Class II · 2 months ago
Foundation Medicine, Inc. Hamilton Microlab STAR Liquid Handler recall: Software issue that can cause an increase in spontaneous software closures
Software issue that can cause an increase in spontaneous software closures.
-
Class II · 2 months ago
Brand Name: Kico Knee Innovation Product Name: Arvis Surgical recall: Due to an internal sensor issue, image displayed with eyepiece may appear
Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
-
Class II · 2 months ago
Tobii Dynavox Llc TD Navio Midi Speech Generating Device Model/ recall: Under certain conditions, the battery mounting tabs may become damaged
Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading…
-
Class II · 2 months ago
Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System recall: Due to a firmware defect, the portable organ transfer device datalogger
Due to a firmware defect, the portable organ transfer device datalogger may lose its configuration, resulting in a blank screen and loss of displayed…
-
Class II · 2 months ago
Siemens Healthcare Diagnostics, Inc. Syva EMIT 2000 Quinidine Assay REF: 4Q019UL recall: Due to unacceptable precision performance exhibited in certain lots
Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated…
-
Class II · 2 months ago
restor3d Inc. Brand Name: Veritas Standard Reverse Total Shoulder Product Name recall: Due to incorrect machining of peripheral screw hole resulting in potential
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
-
Class II · 2 months ago
Gentherm Medical, LLC Blanketrol II Model 222S recall: Overheating of the 115V CPU board may cause the device to shut down
Overheating of the 115V CPU board may cause the device to shut down.
-
Class II · 2 months ago
Siemens Healthcare Diagnostics, Inc. Beckman Coulter recall: Due to unacceptable precision performance exhibited in certain lots
Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated…
-
Class II · 2 months ago
American Contract Systems medical procedure kits and trays labeled recall: The recall notice was initiated due to a Medicom Urgent Medical Device
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges…
-
Class II · 2 months ago
Intersurgical Inc One-Piece Guedel Airway, size 00, ISO 5.0 recall: Devices could potentially be occluded or partially occluded
Devices could potentially be occluded or partially occluded.