FDA Devices recall · Reported March 25, 2015
MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis.
Product may have separating or protruding sponges
Baxter Healthcare Corp. recalled MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis. - a moderate-severity action.
MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis. was recalled by Baxter Healthcare Corp. in March 25, 2015. Reason: Product may have separating or protruding sponges. Check the official notice for the remedy. Verify recall #Z-1269-2015 with the FDA Devices before acting.
The recall
Baxter Healthcare Corp. issued this moderate-severity FDA Devices recall-Product may have separating or protruding sponges.
- Moderate
- severity level
- 4.4M units
- affected scope
- Class II
- classification
- March 25, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1269-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1269-2015) was formally reported on March 25, 2015, with the manufacturer initiating the action on January 22, 2015. It is classified under Moderate severity (Class II), with a current status of Completed. Baxter Healthcare Corp. is listed as the recalling firm, operating out of Deerfield, IL. Federal records list the affected scope as 4,391,520 units, placing this recall in the million-unit bracket that typically triggers nationwide consumer alerts and retailer sweeps.
The documented reason for this recall is: Product may have separating or protruding sponges Distribution data in the federal record shows the product reached: Worldwide Distribution - Nationwide Distribution and to the countries of : Canada, Austria, Norway, Portugal, Saudi Arabia and Spain.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,861 medical devices recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis.
Reason for recall
Product may have separating or protruding sponges
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Completed |
| Recall number | Z-1269-2015 |
| Date reported | March 25, 2015 |
| Date initiated | January 22, 2015 |
| Recalling firm | Baxter Healthcare Corp. |
| Firm location | Deerfield, IL |
| Affected scope | 4,391,520 units |
| Distribution | Worldwide Distribution - Nationwide Distribution and to the countries of : Canada, Austria, Norway, Portugal, Saudi Arabia and Spain. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1269-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Methodology · Corrections · Archive as of August 2026