BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324
Reported: December 18, 2024 Initiated: November 14, 2024 #Z-0671-2025
Product Description
BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324
Reason for Recall
Due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, which can lead to: 1) Unintended and incorrect medication removal, or 2) Potential for a different medication (medication pulled in error) to be refilled/loaded, which may lead to may lead to low inventory or a stockout.
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 40,763
- Distribution
- Worldwide - US Nationwide distribution including in the states of OK, LA, FL, AR, VA, KY, PA, AL, NC, CA, MN, AK, TX, MI, ME, OH, OR, NY, IL, RI, GA, WI, NH, KS, CO, WA, MO, MD, AZ, SC, NV, WV, NM, IN, NJ, TN, DE, MT, MA, VT, DC, NE, CT, ID, WY, MS, UT, HI, IA, SD, ND, GU, MP, PR and the countries of CA, BR, JP, ES, NZ, AU, FR, AR, MX, IT, CL, TR, SA, MY, CH, IE, TH, SG, KW, BE, DE, PT, QA, MA, FI, AE, EG, BS, GB, BM, GR, BH, KR, MC, PL, LB, HK, IN, IL, MO, IQ, TN, NO, PH, CO, TW, CN, JO, OM.
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324. Recalled by CareFusion 303, Inc.. Units affected: 40,763.
Why was this product recalled? ▼
Due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, which can lead to: 1) Unintended and incorrect medication removal, or 2) Potential for a different medication (medication pulled in error) to be refilled/loaded, which may lead to may lead to low inventory or a stockout.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 18, 2024. Severity: Moderate. Recall number: Z-0671-2025.
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