FDA Device recall Z-2268-2012
Mini-Infuser Model 150XL Single Speed Infusion Pump, an Rx battery operated syringe infusion pump
- FDA Device
- Class III
- terminated
- Published 2012-09-05
On 2012-09-05 the FDA classified a Class III recall of Mini-Infuser Model 150XL Single Speed Infusion Pump, an Rx battery operated syringe infusion pump by Baxter Healthcare, citing should a battery with the minimum contact diameter (.51 inches) be placed on the battery spring (.53 inches), an electrical circuit will not be completed and the Mini-Infuser will….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2268-2012 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2011-03-04 |
| Published | 2012-09-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baxter Healthcare |
| Distribution | n/a |
Product
Mini-Infuser Model 150XL Single Speed Infusion Pump, an Rx battery operated syringe infusion pump; Product Usage: These product codes includes refurbished units. Intended for the controlled rate delivery of small volume parental fluids as prescribed by a physician. Usage: The Mini-Infuser System is designed for controlled intermittent administration of intravenous medication.
Reason
Should a battery with the minimum contact diameter (.51 inches) be placed on the battery spring (.53 inches), an electrical circuit will not be completed and the Mini-Infuser will not operate. The reason being that the Mini-Infuser Battery Spring has a flat contact that measures .53 inches ¿.01 inches on the inner diameter of the spring coil. The IEC 60086-2 and ANSI 08 standards specify a minimum
Identifiers
| code_info | product codes 2M8170 and 2M8170R, all serial numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2268-2012%22
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