Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit
Reported: August 8, 2012 Initiated: April 17, 2012 #Z-2131-2012
Product Description
Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit
Reason for Recall
The firm initiated the recall due to a molding defect in a high pressure stopcock where a small percentage of the side ports could become totally occluded.
Details
- Recalling Firm
- ICU Medical, Inc.
- Units Affected
- N/A
- Distribution
- Nationwide distribution
- Location
- San Clemente, CA
Frequently Asked Questions
What product was recalled? ▼
Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit. Recalled by ICU Medical, Inc.. Units affected: N/A.
Why was this product recalled? ▼
The firm initiated the recall due to a molding defect in a high pressure stopcock where a small percentage of the side ports could become totally occluded.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 8, 2012. Severity: Moderate. Recall number: Z-2131-2012.
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