Thoracentesis/ Paracentesis Kit 10/CS; STERILE;
Reported: April 25, 2018 Initiated: February 23, 2017 #Z-1426-2018
Product Description
Thoracentesis/ Paracentesis Kit 10/CS; STERILE;
Reason for Recall
The integrity of the sterile packaging is potentially compromised.
Details
- Recalling Firm
- Carefusion 2200 Inc
- Units Affected
- 1200 units
- Distribution
- Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam
- Location
- Vernon Hills, IL
Frequently Asked Questions
What product was recalled? ▼
Thoracentesis/ Paracentesis Kit 10/CS; STERILE;. Recalled by Carefusion 2200 Inc. Units affected: 1200 units.
Why was this product recalled? ▼
The integrity of the sterile packaging is potentially compromised.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 25, 2018. Severity: Moderate. Recall number: Z-1426-2018.
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