Z-0573-2022 Class II Ongoing
FDA device recall Z-0573-2022 was initiated by Baxter Healthcare Corporation on Jan 7, 2022 and is designated Class II. 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… The recall status is ongoing. Affected quantity: 61,290 units.
Recall Details
- Product Type
- Devices
- Report Date
- Feb 16, 2022
- Initiation Date
- Jan 7, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 61,290 units
Product Description
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, 5C4482EJ
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.
Distribution Pattern
Worldwide
Code Information
All lot numbers within expiry
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0573-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026