Z-1739-2024 Class II Ongoing
FDA device recall Z-1739-2024 was initiated by Cardinal Health 200, LLC on Mar 27, 2024 and is designated Class II. Reason for recall: Cardinal Health is issuing a lot number specific voluntary removal of Jackson-Pratt 3-Spring Reservoir kits due to specific products being shipped to users before undergoing sterilization. The recall status is ongoing. Affected quantity: 98 cases of 12.
Recall Details
- Product Type
- Devices
- Report Date
- May 8, 2024
- Initiation Date
- Mar 27, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 98 cases of 12
Product Description
Jackson-Pratt 3-Spring Reservoir with Silicone Adapters, 400mL, REF SU130-475
Reason for Recall
Cardinal Health is issuing a lot number specific voluntary removal of Jackson-Pratt 3-Spring Reservoir kits due to specific products being shipped to users before undergoing sterilization.
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Panama, Guatemala, Chile, Caribbean Island, Costa Rica.
Code Information
UDI/DI 50885380113114 (Case), 10885380113116 (Each), Lot Numbers: 231251D5
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1739-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026