# FDA recall Z-1213-2023

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2023-02-01.

## Product

Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory to disposable administration set for peritoneal dialysis

## Reason for recall

MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. This could lead to exposure to air, resulting in insufficient iodine/dry sponge inside the MiniCap, which could lead to the potential for inadequate disinfectant.

## Distribution

US Nationwide distribution and Canada.

## Key facts

- **Recall number:** Z-1213-2023
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-01
- **Report date:** 2023-03-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1213-2023

## Citation

> AI Analytics. FDA recall Z-1213-2023. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-1213-2023. Source: US FDA. Licensed CC0.

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