Baxter Infusion Pumps Recalled for Battery Performance Issues
Baxter Healthcare is recalling 589,704 infusion pumps due to battery performance issues related to prolonged storage.
- Product
- Infusion Pump
- Category
- Medical Device
- Distribution
- 52 states
Hazard
1 recall in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 1 battery performance recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all battery performance recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
Baxter Healthcare is recalling 589,704 infusion pumps due to battery performance issues related to prolonged storage.