Data Foundry

Medical device recalls 2014

Hudson RCI¿ Pediatric Anesthesia Breathing Circuits — Class I medical device recall Z-2714-2014

Terminated recall by Teleflex Medical, reported 2014-10-08, distributed nationwide. The pediatric breathing circuits can crack prior to and during use.

Recall numberZ-2714-2014
Product typeMedical device
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTeleflex Medical, Durham, NC, United States
Recall initiated2014-09-08
Classified2014-09-30
Reported by FDA2014-10-08
Terminated2016-08-16
DistributedNationwide (US)
Countries outside the USBE, CA, CL, CN, CO, KR, MX, PE, VE
Quantity27,176 units
Reason classespackaging
Lot numbers0241300618, 02B1400324, 02D1300584, 02E1300090, 02E1300623, 02E1301378, 02E1301383, 02E1301867, 02E1301891, 02E1301892, 02F1300085, 02F1300100, 02F1300101, 02F1300102, 02F1300177, 02F1300729, 02F1302029, 02F1302047, 02F300180, 02FF1300098, 02G1300088, 02G1300296, 02G1300861, 02H1300172, 02H1300454, 02H1301128, 02H1301838, 02J1300876, 02J1302412, 2G1300879

Product

Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Ypiece.

Reason for recall

The pediatric breathing circuits can crack prior to and during use.

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-2714-2014. 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.