Every recall we track for CareFusion 303, Inc. — 139 in all — plus the complaints and injury reports the public filed about them.
CareFusion recalls BD Pyxis MedStation ES Tower REF 352 medication cabinets due to fingerprint scanner overheating that may cause 1st degree burns. Affected units have specific serial numbers.
CareFusion recalls BD Pyxis MedBank Mini REF 1147-0: Fingerprint scanner may overheat causing 1st degree burns. Affected units have specific serial numbers.
CareFusion recalls BD Pyxis MedStation 4000 medication cabinets due to fingerprint scanner overheating that may cause 1st degree burns. Affected units have specific serial numbers.
CareFusion recalls BD Pyxis Anesthesia Station ES REF 327 medication cabinets due to fingerprint scanner overheating potentially causing first-degree burns. Affected units have specific serial numbers.
CareFusion recalls BD Pyxis MedStation ES REF 323 medication cabinets due to fingerprint scanner overheating that may cause 1st degree burns. Affected units have specific serial numbers.
CareFusion recalls BD Pyxis Anesthesia Station 4000 REF: 338 medication cabinets due to fingerprint scanner overheating potentially causing first-degree burns. Affected units have specific serial numbers.
CareFusion recalls BD Pyxis Mini Main REF 349 medication cabinets due to fingerprint scanner overheating that may cause first-degree burns. Affected units have specific serial numbers.
CareFusion recalls BD Pyxis MedBank Tower medication cabinets with serial numbers starting 10885403517167 due to fingerprint scanner overheating that may cause first-degree burns.
CareFusion 303, Inc. is a company that produces medical devices and equipment. They are known for their innovative solutions in the healthcare industry.
Recall of BD Pyxis ES Enterprise Server devices with specific catalog numbers and software versions due to potential failure to receive timely patient and medication updates from enterprise systems.
CareFusion recalls Pyxis MedStation ES models with firmware 1.48 due to potential access delays for medications. Affected units may need updates to prevent medication delays.
Recall of BD Alaris Pump Module model 8100 with specific UDI-DI codes due to potential connectivity problems with hospital networks caused by daylight savings time adjustments.
Recall of BD Alaris infusion pump modules 8100 and related parts due to risk of under/over-infusion if dropped or jarred. Affected units sold after June 19, 2004.
Recalled BD Pyxis Medbank models with reference numbers 1137-00 to 155169-01 may experience fluid ingress leading to smoke, system downtime, or fire. Consumers should check their device serial numbers.
CareFusion recalls all Pyxis CII Safe ES Tower Main units (REF: 111:00) due to potential fluid ingress causing smoke, system downtime, or fire. Affected units have specific serial numbers.
CareFusion recalls BD Pyxis Pro 7-Drawer Auxiliary models with reference numbers 1149-00 and 1152-00 due to potential fluid ingress causing smoke, system downtime, or fire.
CareFusion recalls BD Pyxis MedFlex infusion pumps with specific reference numbers due to risk of fire or smoke from fluid ingress. Affected units may need immediate action.
CareFusion recalls BD Pyxis Pro MedStation Main (REF 115:00) due to potential fluid ingress causing smoke, system downtime, or fire. Affected units have specific serial numbers.
CareFusion recalls BD Alaris Pump Infusion Sets with specific reference numbers due to potential flow rate and bolus accuracy issues that could affect patient safety.
CareFusion 303, Inc. is a leading manufacturer of medical devices and healthcare products. Explore their product catalog for the latest innovations in medical technology.
Recall of BD Alaris Pump Module Model 8100 with Guardrails and Suite MX software versions due to potential flow rate and bolus accuracy issues. Affected units have specific serial numbers.
BD Alaris Pump Infusion Sets with specific model numbers may not deliver medication at correct flow rates or bolus doses, risking incorrect treatment. Affected units include those with back check valves and SmartSite Y-sites.
CareFusion recalls Pyxis medication dispensing systems due to antivirus software not being consistently installed during implementation, which could lead to security vulnerabilities.
CareFusion recalls specific medical software systems that may delay medication access during cabinet upgrades due to software errors after Microsoft patches. Affected users should contact CareFusion for guidance.
CareFusion recalls specific BD PYXIS MEDBANK models due to software error during pocket exchange restocking that could double medication counts and delay access to medicines.
BD Pyxis MedBank CUBIE Replenishment Stations with certain model numbers may show a stock error message when restocking, potentially delaying medication access for patients. Affected units include specific product codes listed in the recall.
BD Pyxis automated dispensing cabinets with software version 2.4 have a bug that can cause incorrect medication counts and extra doses. Affected units include MedBank Mini, Tower, MedFlex, and MedPass models.
CareFusion recalls BD Alaris Systems Manager software versions 12.5.1 and 12.5.2 due to potential outdated automated programming requests for infusion units. Affected units may require updates to prevent safety issues.
CareFusion recalls BD Pyxis Anesthesia Station ES models with specific software versions due to sync errors that could lead to incorrect medication dispensing. Affected units may need software updates to prevent safety issues.
Recalled BD Pyxis MedFlex 2.0 spare parts (REF 353200-01) have fingerprint scanners that heat up due to failure, potentially causing burns. Affected units include specific serial numbers listed in the recall.
CareFusion recalls BD Alaris Pump Module REF 8100 due to user manual error that may cause accidental overinfusion if safety clamp is left open. Affected units include those with software version 12.1.2.
CareFusion recalls BD Pyxis MedStation and Anesthesia Station models with insufficient labeling for medication access delays. Users should check serial numbers and software versions to determine if affected.
CareFusion recalls BD PYXIS MEDBANK TWR MN and MINI models due to a labeling update needed for procedure and operating room use. No immediate action required.
Recall of BD Pyxis MedBank Mini and TWR MN units for labeling update to include contraindication against use in procedures and operating rooms. No action required for safety.
Recall of BD Pyxis Medflex MN 1000 and 2000 models for labeling update to include contraindication against use in procedure and operating rooms.
CareFusion recalls BD PYXIS MEDBANK MINI models with labeling update to include contraindication against use in procedures and operating rooms.
CareFusion recalls Pyxis MedStation ES and Anesthesia Station models with software issues that could cause wrong therapy doses, delays in dispensing, or unauthorized access. Affected units have specific catalog numbers and software versions.
CareFusion 303, Inc. is a leading manufacturer of medical devices and healthcare products. Explore our comprehensive product catalog for the latest innovations in medical technology.
Recall of BD Pyxis CII Safe ES devices with software version 1116-00 due to risk of dispensing incorrect medications, potentially causing medication errors or stockouts. Affected units include specific serial numbers.
CareFusion 303, Inc. - 16344755
CareFusion 303, Inc. is a leading manufacturer of medical devices and healthcare products. Explore their product catalog for detailed information on their latest innovations.
CareFusion 303, Inc. is a company that produces medical devices and equipment. This page lists their product catalog.
CareFusion recalls Alaris EtCO2 Module Model 8300 infusion pumps due to potential bent connectors that could delay infusion starts. Affected units have specific serial numbers and UDI-DI codes.
CareFusion recalls BD Pyxis QFill Replenishment Station (REF: 138904-01) due to potential incorrect medication labels printed for non-CUBIE locations. Affected units have specific serial numbers.
CareFusion recalls Pyxis QFill Replenishment Station with potential for incorrect medication labels when restocking non-CUBIE locations. Affected units have specific serial numbers; contact CareFusion for remedy.
CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 for potential incorrect medication bin labeling during restocking. Affected units may need software update to prevent errors.
CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 for potential incorrect medication bin labeling during restocking. Affected units have specific serial numbers and UDI.
CareFusion recalls BD PYXIS MEDBANK TWR units with software version 3.9.1.9 due to potential incorrect medication bin labeling in automated dispensing cabinets.
CareFusion recalls BD PYXIS MEDBANK TWR MN software version 3.9.1.9 due to potential incorrect medication bin labels during restocking. Affected units have specific serial numbers and model codes.
CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 for potential incorrect medication bin labeling during restock. Affected units have specific serial numbers and model codes.
CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 for potential incorrect medication bin labeling during restocking. Affected units include specific serial numbers and model codes.
Recall of BD Pyxis MEDBANK Mini CR-4HH-P units with software version 3.9.1.9 due to potential printing of incorrect medication bins. Affected units have specific serial numbers.
CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 due to potential incorrect medication bin printing on restock labels. Affected units have specific serial numbers and model codes.
CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 where restock labels may show wrong medication bins. Affected units have specific serial numbers and UDI codes.
CareFusion recalls BD PYXIS MEDBANK TWR units with software version 3.9.1.9 for potential incorrect medication bin labeling during restock. Affected units have specific serial numbers and UDI.
CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 due to potential incorrect medication bin printing. Affected units may mislabel medications in automated dispensing cabinets.
