Data Foundry

Medical device recalls 2021

Stopcock rotator — Class II medical device recall Z-1477-2021

Terminated recall by Smiths Medical ASD Inc., reported 2021-04-28, distributed nationwide. Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds, Stopcocks and Tubing and Medex LogiCal Kit

Recall numberZ-1477-2021
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSmiths Medical ASD Inc., Minneapolis, MN, United States
Recall initiated2021-03-31
Classified2021-04-21
Reported by FDA2021-04-28
Terminated2023-03-20
DistributedNationwide (US)
Countries outside the USAT, BR, CA, CL, CO, EC, HK, JP, MX, SI, ZA
Quantity3,825 units
Lot numbers3971467, 3987918, 3995544, 3995545, 4011838, 4027758, 4033501, 4044959
Model numbers1050, 700PSI, MX1431MR, MX1431MRL, MX4331R

Product

Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR, OFF HANDLE, Model Number MX1431MR b. 1050 STOPCOCK LEFT ROTATOR, OFF HANDLE, Model Number MX1431MRL c. 700 PSI STPCK W/ ROTATOR, Model Number MX4331R. Stopcocks and manifolds used to control the direction of IV fluid flow.

Reason for recall

Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds, Stopcocks and Tubing and Medex LogiCal Kits may have been manufactured with insufficient or incomplete welds. These are components for various cardiac kits including pressure monitoring devices and interventional imaging devices.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1477-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.