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RecallWatchMedical Device Safety
Class IIOngoingZ-1123-2025

CareFusion 303, Inc. recalls BD Pyxis MedStation Auxiliary ES REF: 324. Intended to securely store and dispense med…

CareFusion 303, Inc.San Diego, CA, United StatesReported Feb 19, 2025 · 1 year ago
Legal News Analyst ·

Reason for recall

Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • BD Pyxis MedStation Auxiliary ES REF: 324. Intended to securely store and dispense medications to a qualified and authorized healthcare providerUDI
    UDI 10885403512681/
    400 affected lots
    1618386916183877161813081618130916184719161847201615521416167998
    +392 more1617371116173716161737241617372516173726161737271617372816156524161565291616341216163413161634161616341716163418161634201615594516182183161822951618229816184712161873321617352116173523161905511619055216190553161905541616759216185663161885501618855116188560161885611617343716173439161039491617352216177055161770561617368016173681161737141617371716173718161737191617372116173722161737231617791016185638161886021618860316192625161926341618218116182185162008121616940116167449161679961616274116162739161627421616274316162744161627451616132016161322161613241616752216194353161838411618384316195336161565211614408916144090161440951614409616145983161675811616758316167585161675871616758916192307161923091619262216192627161926311610257916196727161967291619662616195229161926301619664916192240161736151617361616177914161986831619436316195232161821791618218016182182161822921618229616182297161644981619230816155092161533741615509316155086161495671614956816168891161688931616107516161077161099541616108216161083161838811618414716184177161953321619533416195338161559661615596716155968161873071618731216187314161873181616735116195841161838681618387916200806161674571618770216187716161877181618772016187722161877251618773216187736161903081619666416198551162008271620082816200831160809771616744516167446161725141616252916161071161610731616107616188224161882251618415016184162161613491616135016183849161838501614670216187738161877391618774216187743161877441618774516187746160485321604853316176335161763361617701416177020161770211617702616177041161770421617704316188975161889781618561216185613161856161618561916185620161856221617783016177833161778351617783616177837161778421617784416167650161673401614950916180596161805971618059816173623161736241617362516173627161736281617362916173630161736311617363216147475161805321616450516173753161905551619055616190558161905601620696716163221161632221616322316163224161632251616322616163227161632281616322916163230161632311608765216087653160876541608765516087656161923251616746316164506161674641619585016199855161998561619985816194317161943181619432316194324161943251618381016164531161645321616453716183815161838171618065716184788161847901618479116183990161839921618400016184021161840221618402416173475161838211618383816183842161922341619223516192245161922681619227116192292161890491620577316205771162057051614917616167514161839991619527116195272161952731619527416195275161856541618565616180609161806101618061316180614161806161618061716180619161806201618062816180630161688771619583616195843161958441620576616166735161667361616674216192867161856051618560616185608161856271618562916185631161856331612847016199219161886171618861816199962161692101616921216169214161692151616921616169217161692181616921916169220161692231616922416199847161998491619985016199851161886381618863916194355162039201611641016192653161926541619265516192656161926571619265816192659161926601619266116192662161926631619266416192665161926661619266716192668161926691619267016192671161959021619590816187706161877071618765216203877162038791616744216167443161674471616744816203769161627401614665616146657161466601617785616178058161780621617806816178072

What the firm is doing

On February 14, 2023 and January 9. 2024 Carefusion issued a Urgent medical Device Product Advisory" Recall Notification to affected consignees. Carefusion asked consignees take the following actions: 1. Customers may continue to use these devices as intended and should file a complaint via the Customer Portal at https://www.bd.com/self-service or call BD Support at 1-800-727-6102, should you experience drawer or door failures. 2. If you experience delays in access to medication due to a drawer or door failure, ensure backup procedures (which may include but may not necessarily be limited to keys, emergency medication supplies, alternate devices in proximity, etc.) are in place and staff have all been properly trained on them. 3. Please promptly complete and return the enclosed Customer Response Form to acknowledge receipt of this notification and that you understand the information provided in this letter. 4. If you have specific questions about this letter, please contact 1-866-583-8783. 5. Any adverse health consequences experienced with the use of this product should be reported to BD and may be reported to the FDA s MedWatch Adverse Event Reporting Actions to be taken by distributor 1. Please provide a copy of this notification to any customers who may have received products listed in the Affected Products table above. 2. Please promptly complete and return the enclosed Customer Response Form to acknowledge receipt of this notification and that you understand the information provided in this letter.

DistributionShow details

US: Nationwide OUS:JP IT IN DE GB KR NL TW ES BE AU BH CA BR NZ FR AR QA MX CL TR SA MY CH IL IE TH SG KW MA FI AE EG BS BM GR MC PL LB MO IQ TN NO PH CN HK CO JO OM

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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