RS 5F DL XPP, Catalog Number 60M030393
FDA Recall Z-2201-2018 · Posted None
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Recalling FirmAngiodynamics Inc. (Navilyst Medical Inc.)
Recall StatusTerminated
Product CodeLJS
Date Initiated2018-05-10
Date Terminated2020-05-13
Product Quantity7 boxes
Reason for Recall
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Firm Action
Urgent Medical Device Recall letters were sent to customers on 5/10/18. The letters instructed customers to do the following:
IMMEDIATELY
Stop using the product subject to recall.
Remove any affected (recalled) product from your inventory (whether in labs, Central Supply, Shipping and Receiving or ANY other location).
Segregate this product in a secure location for return to AngioDynamics, Inc.
Forward a copy of this recall notification to all sites to which you have distributed affected product.
Complete and return the Reply Verification Tracking Form.
If affected product is located in your institution, please call AngioDynamics Customer Service at 1-800-772-6446 between 8:00 a.m. and 7:00 p.m. (Monday Friday: Eastern Standard Time) to obtain a replacement or credit for your returned product.
Root Cause
Material/Component Contamination
Distribution Pattern
The products were distributed to the following US states: AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, WA, WI, and WV. The products were distributed to the following foreign countries: Canada, China, Ireland, Spain.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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