Data Foundry

Medical device recalls 2021

Mark 910 LogiCal — Class II medical device recall Z-1471-2021

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-1471-2021
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
Quantity10 devices
Lot numbers4031331
Model numbersDPS567201

Product

Mark 910 LogiCal, Model Number DPS567201. for blood pressure monitoring and blood sampling.

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-1471-2021. 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.