Vantive Us Healthcare Llc
Complete recall history across all FDA and CPSC categories — 12 total recalls
Vantive Us Healthcare Llc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (12)
FDA medical device enforcement actions by Vantive Us Healthcare Llc
| Date | Product | Reason | Class |
|---|---|---|---|
| Jan 6, 2026 | PRISMAFLEX HF1000 SET, Product Code 107142; Dialyzer, High Permeability With ... | There is a potential dislodgement of the Prismaflex Set deaeration chamber fr... | Class II |
| Jan 6, 2026 | PRISMAFLEX ST150 SET US, Product Code 107640US; Dialyzer, High Permeability W... | There is a potential dislodgement of the Prismaflex Set deaeration chamber fr... | Class II |
| Jan 6, 2026 | PRISMAFLEX HF1000 SET, Product Code 107140; Dialyzer, High Permeability With ... | There is a potential dislodgement of the Prismaflex Set deaeration chamber fr... | Class II |
| Jan 6, 2026 | PRISMAFLEX TPE2000 SET, Product Code 114093; Dialyzer, High Permeability With... | There is a potential dislodgement of the Prismaflex Set deaeration chamber fr... | Class II |
| Jan 6, 2026 | PRISMAFLEX M150 SET, Product Code 109990; Dialyzer, High Permeability With Or... | There is a potential dislodgement of the Prismaflex Set deaeration chamber fr... | Class II |
| Jan 6, 2026 | OXIRIS SET, Product Code 112016; Dialyzer, High Permeability With Or Without ... | There is a potential dislodgement of the Prismaflex Set deaeration chamber fr... | Class II |
| Jan 6, 2026 | PRISMAFLEX ST100 SET US, Product Code 107636US; Dialyzer, High Permeability W... | There is a potential dislodgement of the Prismaflex Set deaeration chamber fr... | Class II |
| Jan 6, 2026 | PRIMSAFLEX M100 SET, Product Code 106697; Dialyzer, High Permeability With Or... | There is a potential dislodgement of the Prismaflex Set deaeration chamber fr... | Class II |
| Aug 28, 2025 | Sharesource Connectivity Platform for Use with Homechoice Claria Product C... | Vantive has identified a software defect within the Sharesource Claria softwa... | Class II |
| Jul 28, 2025 | PrisMax V3 control Unit-US, Hemodialysis Delivery System, Product Code 955724 | Unexpected PrisMax System alarm T0830: Blood Leak Detected, when no blood lea... | Class II |
| Jul 28, 2025 | TherMax Blood Warmer Unit-US, PrisMax Accessory, Product Codes: 955630, 9555... | Thermax System may be unable to detect the presence of a bag on the Thermax B... | Class II |
| Jul 28, 2025 | PrisMax V2-US, Hemodialysis Delivery System, Product Codes: 955626, 955558, ... | Low deaeration chamber level at post priming tests may lead to PrisMax System... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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