Civco Medical Instruments Co. Inc.: Medical Device Recall in 2018 - (Recall #: Z-2947-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

CIVCO Needle Guide, REF 676-150, QTY 24, STERILE EO

Product Classification:

Class II

Date Initiated: July 30, 2018

Date Posted: September 5, 2018

Recall Number: Z-2947-2018

Event ID: 80656

Reason for Recall:

The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide.

Status: Terminated

Product Quantity: 3 units

Code Information:

UDI 00841436107334, Lot numbers: A035054, A042207

Distribution Pattern:

United States, Austria, Belgium, Denmark, France, Germany, Poland, Spain, Switzerland and United Kingdom

Voluntary or Mandated:

Voluntary: Firm initiated