Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
Reported: January 15, 2025 Initiated: November 22, 2024 #Z-0820-2025
Product Description
Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
Reason for Recall
The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.
Details
- Recalling Firm
- Nipro Renal Soultions USA, Corporation
- Units Affected
- 2,810 units
- Distribution
- US distribution to states of: AZ, FL, GA, GA, IL, MI, NC, NJ, OH, TN, TX.
- Location
- Lewisberry, PA
Frequently Asked Questions
What product was recalled? ▼
Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25. Recalled by Nipro Renal Soultions USA, Corporation. Units affected: 2,810 units.
Why was this product recalled? ▼
The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 15, 2025. Severity: Moderate. Recall number: Z-0820-2025.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11