Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack
Reported: November 1, 2023 Initiated: September 20, 2023 #Z-0147-2024
Product Description
Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack
Reason for Recall
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Details
- Recalling Firm
- Cardinal Health 200, LLC
- Units Affected
- 3,084,300 units
- Distribution
- US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.
- Location
- Waukegan, IL
Frequently Asked Questions
What product was recalled? ▼
Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack. Recalled by Cardinal Health 200, LLC. Units affected: 3,084,300 units.
Why was this product recalled? ▼
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 1, 2023. Severity: Critical. Recall number: Z-0147-2024.
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