Data Foundry

Medical device recalls 2017

Smiths Medical CADD Blue-Striped IV Administration Set — Class II medical device recall Z-2759-2017

Terminated recall by Smiths Medical ASD Inc., reported 2017-08-02. The label of the CADD Blue-Striped Administrative Set is missing the expiration date, which is considered a re

Recall numberZ-2759-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSmiths Medical ASD Inc., Minneapolis, MN, United States
Recall initiated2016-12-09
Classified2017-07-24
Reported by FDA2017-08-02
Terminated2017-12-14
Countries outside the USCA
Quantity641,070 units
Reason classeslabeling
Lot numbers010X47, 025X47, 064X46, 079X48, 094X46, 103X46, 108X49, 155X40, 170X47, 173X47, 187X49, 193X45, 208X40, 208X45, 217X46, 224X46, 230X44, 241X40, 268X40, 286X40, 41X065, 41X099, 41X173, 41X221, 41X284, 41X302, 41X366, 41X399, 41X506, 42X047, 42X154, 42X238, 42X259, 42X266, 42X302, 42X393, 42X505, 431X40, 43X013, 43X099 and 43 more
Model numbers21-7036-01

Product

Smiths Medical CADD Blue-Striped IV Administration Set, REF 21-7036-01, Sterilized using ethylene oxide.

Reason for recall

The label of the CADD Blue-Striped Administrative Set is missing the expiration date, which is considered a regulatory compliance issue for Canada.

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-2759-2017. 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.