Baxter Healthcare Corporation Recall 86788
Description: Infusion Pump
Baxter Healthcare Corporation Recall 86788 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-1150-2021 |
| Event ID | 86788 |
| Event Description | Infusion Pump |
| Product Type | Devices |
| Distribution | Domestic Distribution: ST, AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and Puerto Rico. International Distribution: Canada, Barbados, Bermuda, St. Thomas, Guyana, Trinidad and Tobago, Jamaica and Nassau Bahamas. |
| Quantity | 589,704 total units |
| Recall Reason | Battery performance issues related to prolonged storage. |
| Device Classification | 20210303 |
| Device Code Info | Infusion Pump Product codes: 35700ABB, 35700BAX, and 35700BAX2 Battery codes: 35083, 35162, 35195, and 35724. Infusion Pump Product codes: 35700ABB, 35700BAX, 35700BAX2 3570009 Battery codes: 35223 and 36010 |
| Center Classification Date | 20210225 |
| Recall Initiation Date | 20210106 |
| Recalling Firm | Baxter Healthcare Corporation |
| Initial Notification | Letter |
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