Z-0948-2022 Class II Terminated
FDA device recall Z-0948-2022 was initiated by Baxter Healthcare Corporation on Feb 25, 2022 and is designated Class II. Reason for recall: Product is mislabeled as self-righting Luer slip tip caps, yellow. The recall status is terminated (terminated Mar 2, 2026). Affected quantity: 5,500 DISCPACs (100/DISCPAC).
Recall Details
- Product Type
- Devices
- Report Date
- Apr 27, 2022
- Initiation Date
- Feb 25, 2022
- Termination Date
- Mar 2, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5,500 DISCPACs (100/DISCPAC).
Product Description
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
Reason for Recall
Product is mislabeled as self-righting Luer slip tip caps, yellow.
Distribution Pattern
Worldwide distribution - US Nationwide distribution in the states of FL, GA, IL, IN, MO, PA, TX, and VA. The countries of Canada, Austria, Germany, Netherlands, Qatar, Saudi Arabia, and Spain.
Code Information
Lot numbers 60268365, 60268609, 60268610, exp. date 10/31/2023; UDI 0085412478852.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0948-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026