# FDA recall Z-1639-2025

> **CareFusion 303, Inc.** · Class II · device recall initiated 2025-03-11.

## Product

BD PYXIS MEDBANK (Name, REF):  MEDPASS MODULE, 139088-01;  MINI 1FH-1FM, 169-137;  MINI 1HH-1FH-1HM, 169-101;  MINI 1HH-1HM-1FM, 169-102;  MINI 2FH, 138902-01;  MINI 2FH, 169-104;  MINI 2FM, 169-105;  MINI 2HH-1FH, 169-106;  MINI 2HH-1FH, 138908-01;  MINI 2HH-1FM, 169-107;  MINI 2HH-1FM, 138906-01;  MINI 3HH-1FG, 169-110;  MINI 3HH-1FG, 139091-01;  MINI 3HH-1HM, 169-111;  MINI 4HH, 138910-01;  MINI 4HH, 169-112;  MINI 4HM, 169-113;  MINI 4HM, 138915-01;  TWR MN 10HH-1FH-1FM, 169-23;  TWR MN 10HH-2FH, 169-24;  TWR MN 10HH-2FH, 138955-01;  TWR MN 10HH-2FM, 169-25;  TWR MN 10HH-2FM, 138924-01;  TWR MN 12HH-1FF, 169-26;  TWR MN 12HH-1FF, 138960-01;  TWR MN 12HH-1FH, 169-27;  TWR MN 12HH-1FH, 138961-01;  TWR MN 12HH-1FM, 169-28;  TWR MN 12HH-1FM, 138926-01;  TWR MN 14HH, 138927-01;  TWR MN 14HH, 169-29;  TWR MN 1HH-1HM-2FM-4FF, 169-30;  TWR MN 2FH-2HM-4FM, 169-31;  TWR MN 2HH-10HM-1FM, 169-32;  TWR MN 2HH-1FH-5FM, 169-33;  TWR MN 2HH-2FH-4FM, 169-34;  TWR MN 2HH-4FH-2FM, 169-139;  TWR MN 2H

## Reason for recall

Users trying to restock a single bin location of an automated dispensing cabinet, during pocket exchange restocking workflow, may experience a software issue that results in 2 destock transactions and 2 stock transactions, which results in doubling the bin quantity, which may result in a delay in access to desired medications and/or supplies, which may lead to temporary body function impairment.

## Distribution

US Nationwide distribution including in the states of MO, MI, FL, PA, SC, OR, AZ, CO, ND, GA, NE, TX, IL, OH, VT, IN, TN, KY, IA, MT, NY, CA, UT, OK, SD, WA, AK, ME, NV, NM, NC, WV, LA, MN, ID, AL, VA, WI, NH, KS, MA, CT, RI, NJ, MD, MS, WY, DC, DE, HI, AR, ON.

## Key facts

- **Recall number:** Z-1639-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-11
- **Report date:** 2025-04-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1639-2025

## Citation

> AI Analytics. FDA recall Z-1639-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1639-2025. Source: US FDA. Licensed CC0.

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