CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187
Reported: September 11, 2019 Initiated: July 10, 2019 #Z-2471-2019
Product Description
CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187
Reason for Recall
The filter capacity is not achieved due to damage of the filter membrane.
Details
- Recalling Firm
- B. Braun Medical, Inc.
- Units Affected
- 200 units
- Distribution
- CA FL MO TX MN AL GA NC IL PA
- Location
- Allentown, PA
Frequently Asked Questions
What product was recalled? ▼
CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187. Recalled by B. Braun Medical, Inc.. Units affected: 200 units.
Why was this product recalled? ▼
The filter capacity is not achieved due to damage of the filter membrane.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 11, 2019. Severity: Moderate. Recall number: Z-2471-2019.
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