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Verathon, Inc. recalls BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the bl
Recalled December 9, 2020 · FDA recall Z-0531-2021 · Verathon
Hazard
Due to a change in handle material and process, probe handle may crack. · FDA Class II
Units
398 units
Sold at
Worldwide distribution - U.S. Nationwide distribution including in the states of AL, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, NC, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WI, WV and WY. The countries of Austrailia, Belgium, Canada, France, Germany, Kuwait, Luxembourg, New Zealand, Portugal, Singapore, Sweden, Switzerland, Taiwan, and United Kingdom.
Description
Due to a change in handle material and process, probe handle may crack.
Product
BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the bladder noninvasively.
Manufacturer(s)
Verathon, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →