Cardinal Health 200, LLC: Medical Device Recall in 2018 - (Recall #: Z-2491-2018)

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:

Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Double Spike, Ref ASU1201, packaged 1/box, 12 boxes/case, single use, RX, Sterile.

Product Classification:

Class II

Date Initiated: June 11, 2018

Date Posted: July 25, 2018

Recall Number: Z-2491-2018

Event ID: 80288

Reason for Recall:

The suction valve may not close properly which could cause continuous suction.

Status: Terminated

Product Quantity: A total of 63,020 valves were distributed. Specific product quantities were not provided.

Code Information:

Lot numbers 31712, 31711, 31713, 31714, 31764, 31765, 41711, 41713, 41715, 41724, 41737, 41714, 41721, 41722, 41723, 41727, 41726, 41725, 41719, 41731, 41732, 41730, 41728, 41733, 41734, 41735, 71738, 71739, 71740, 71748, 71741, 71742, 81745, and 71743.

Distribution Pattern:

Distribution was made to AL, AR, AZ, CA, CO, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MI, MN, MO, MT, NC, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, and WY. Government and military distribution was also made. Foreign distribution was made to Belgium, France, Germany, Israel, Italy, Netherlands, Singapore, and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated