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Recall

Class II — Civco Medical Instruments Co. Inc.

Recalling firmCIVCO Medical Instruments Co., Inc.
Registered facilityCIVCO Medical Instruments Co., Inc. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonA cover failed leak testing during validation testing of new needle guides from a replacement tool.
ProductCIVCO lnfiniti Needle Guide Bracket. used for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducers. Product Usage: The bracket and disposable guide provide physicians with a tool for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducers.
Quantity177 boxes
DistributionWorldwide Distribution - US Nationwide in the states of GA, KY, CA, NY , NJ, TX, IL, MA, RI, AZ, and IA and countries of Ukraine, Hong Kong, Italy, Netherlands, Switzerland, United Kingdom, Denmark, Germany, Belgium, Spain, Japan, China, and Canada
Initiated2018-02-23
Classified2018-08-22
Terminated2020-10-06
Recall numberZ-2888-2018
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Civco Medical Instruments Co. Inc. (Z-2888-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80704/

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