FDA Medical devices recall ·
BD Pyxis MedStation Auxiliary ES recall
- Recall number
- Z-1123-2025
- Date
- (initiated February 23, 2024)
- Company / brand
- CareFusion 303, Inc.
10020 Pacific Mesa Blvd, San Diego, CA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
BD Pyxis MedStation Auxiliary ES REF: 324. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI: 10885403512681/ Serial Numbers: 16183869 16183877 16181308 16181309 16184719 16184720 16155214 16167998 16173711 16173716 16173724 16173725 16173726 16173727 16173728 16156524 16156529 16163412 16163413 16163416 16163417 16163418 16163420 16155945 16182183 16182295 16182298 16184712 16187332 16173521 16173523 16190551 16190552 16190553 16190554 16167592 16185663 16188550 16188551 16188560 16188561 16173437 16173439 16103949 16173522 16177055 16177056 16173680 16173681 16173714 16173717 16173718 16173719 16173721 16173722 16173723 16177910 16185638 16188602 16188603 16192625 16192634 16182181 16182185 16200812 16169401 16167449 16167996 16162741 16162739 16162742 16162743 16162744 16162745 16161320 16161322 16161324 16167522 16194353 16183841 16183843 16195336 16156521 16144089 16144090 16144095 16144096 16145983 16167581 16167583 16167585 16167587 16167589 16192307 16192309 16192622 16192627 16192631 16102579 16196727 16196729 16196626 16195229 16192630 16196649 16192240 16173615 16173616 16177914 16198683 16194363 16195232 16182179 16182180 16182182 16182292 16182296 16182297 16164498 16192308 16155092 16153374 16155093 16155086 16149567 16149568 16168891 16168893 16161075 16161077 16109954 16161082 16161083 16183881 16184147 16184177 16195332 16195334 16195338 16155966 16155967 16155968 16187307 16187312 16187314 16187318 16167351 16195841 16183868 16183879 16200806 16167457 16187702 16187716 16187718 16187720 16187722 16187725 16187732 16187736 16190308 16196664 16198
Distribution
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
States: Arkansas California Illinois Missouri Tennessee
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1123-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.