Baxter Equipo de transferencia para DP MiniCap de vida util prolongada con pinza de torsion, 5C4482S
Reported: February 16, 2022 Initiated: January 7, 2022 #Z-0574-2022
Product Description
Baxter Equipo de transferencia para DP MiniCap de vida util prolongada con pinza de torsion, 5C4482S
Reason for Recall
Cleaning products, containing, but not limited to, hydrogen peroxide, bleach, alcohol, or antiseptic agents and solvent, such as those containing acetone, toluene, xylene, or cyclohexanone may cause damage, such as leaking or cracking, to the MiniCap Extended Life PD transfer sets.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 116,628 units
- Distribution
- Worldwide
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Baxter Equipo de transferencia para DP MiniCap de vida util prolongada con pinza de torsion, 5C4482S. Recalled by Baxter Healthcare Corporation. Units affected: 116,628 units.
Why was this product recalled? ▼
Cleaning products, containing, but not limited to, hydrogen peroxide, bleach, alcohol, or antiseptic agents and solvent, such as those containing acetone, toluene, xylene, or cyclohexanone may cause damage, such as leaking or cracking, to the MiniCap Extended Life PD transfer sets.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 16, 2022. Severity: Moderate. Recall number: Z-0574-2022.
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