Z-2741-2020 Class I Terminated
FDA device recall Z-2741-2020 was initiated by CareFusion 303, Inc. on Jun 30, 2020 and is designated Class I. Reason for recall: If one or more screws or washers are loose or missing causing the battery not to be properly secured to the PC Unit, that is running on battery power, the system may experience a power loss with a… The recall status is terminated (terminated Apr 22, 2024). Affected quantity: 824277.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 12, 2020
- Initiation Date
- Jun 30, 2020
- Termination Date
- Apr 22, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 824277
Product Description
Reason for Recall
Distribution Pattern
U.S.: CO, FL, SC, NY, CA, NC, TX, IL, PA, AZ, LA, IN, MA, MO, AR, WI, HI, OR, OH, KS, MN, MI, WA, UT, MD, TN, CO, NJ, NE, ND, WV, KY, IA, MS, AL, DE, AK, VA, OK, NM, GA, CT, SD, NV, ID, MT, ME, VT, WY, NH, MP, DC, GU, PR, AS, RI. O.U.S.: TR, QA, CA, AE, KW, MX, IL, SA, CH, NL, BE, TW, ZA, PH, CN, AU, IN, FR, MY, NZ, GB, KR, PK, DE, SG, JP, CU, BH
Code Information
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2741-2020
- openFDA file date
- Oct 6, 2026
- Loaded by RegDataLab
- Oct 12, 2026