Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent.
Reported: May 1, 2019 Initiated: March 15, 2019 #Z-1202-2019
Product Description
Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent.
Reason for Recall
There is an error in the chromomap included in the labeling for the product.
Details
- Recalling Firm
- Cytocell Ltd.
- Units Affected
- 19
- Distribution
- The products were distributed to the following US states: IL, TN.
- Location
- Adderbury Banbury Oxfordshire, N/A
Frequently Asked Questions
What product was recalled? ▼
Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent.. Recalled by Cytocell Ltd.. Units affected: 19.
Why was this product recalled? ▼
There is an error in the chromomap included in the labeling for the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 1, 2019. Severity: Low. Recall number: Z-1202-2019.
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