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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Baxter Healthcare Corporation: 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.

Agency Publication Date: February 8, 2022
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Affected Products

Product: Baxter CAPD System Transfer Set (CAPD MiniCap Transfer Set II (34cm)), Code No. T5C4484

All lot numbers within expiry

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Product: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, REF R5C4482E

All lot numbers within expiry

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Product: Baxter MiniCap Extended Life PD Transfer Set Twist Clamp - Extra Short, REF R5C4483

All lot numbers within expiry

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Product: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Long, REF R5C4484

All lot numbers within expiry

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Product: Baxter CAPD System Transfer Set (CAPD MiniCap Transfer Set II (24cm)), Code No. T5C4482

All lot numbers within expiry

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Product: Baxter MiniCap Extended Life PD Transfer Set (Easy-Lock), 5C4449

All lot numbers within expiry

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Product: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, 5C4482

All lot numbers within expiry

Lot Numbers:
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Product: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short, 5C4483

All lot numbers within expiry

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Product: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, 5C4482EJ

All lot numbers within expiry

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Product: Baxter Equipo de transferencia para DP MiniCap de vida util prolongada con pinza de torsion, 5C4482S

All lot numbers within expiry

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Product: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, REF R5C4482

All lot numbers within expiry

Lot Numbers:
numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 89327
Status: Active
Manufacturer: Baxter Healthcare Corporation
Manufactured In: United States
Units Affected: 11 products (23,940 units; 2,553,528 units; 344,190 units; 61,290 units; 116,628 units; 449,676 units; 62,712 units; 58,194 units; 13,590 units; 8,928 units; 2,240 units)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.