Data Foundry

Medical device recalls 2023

Magic3 Go Intermittent Urinary Catheters — Class II medical device recall Z-1698-2023

Ongoing recall by C.R. Bard Inc, reported 2023-06-14. Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pou

Recall numberZ-1698-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmC.R. Bard Inc, Covington, GA, United States
Recall initiated2023-04-20
Classified2023-06-08
Reported by FDA2023-06-14
Quantity9,894,922 devices
Reason classeslabeling, sterility
UPC / GTIN / UDI-DI00801741097836, 00801741097850, 00801741097874, 00801741097898, 00801741097935, 00801741098086
Lot numbersJUFV1857, JUFW0450, JUFW1146, JUFW1179, JUFW1753, JUFW2655, JUFW2684, JUFX1968, JUFX1970, JUFX2028, JUFX2030, JUFX2050, JUFX2051, JUFX2811, JUFX2812, JUFX2824, JUFX2825, JUFX2826, JUFX9006, JUFX9008, JUFX9009, JUFX9011, JUFX9028, JUFY1596, JUFY1816, JUFY2609, JUFY9030, JUFZ0451, JUFZ0452, JUFZ0455, JUFZ0781, JUFZ0782, JUFZ0926, JUFZ0927, JUFZ0984, JUFZ0997, JUFZ0998, JUFZ1016, JUGN9126, JUGN9127 and 131 more
Model numbers51808, 51810, 51812, 51814, 51816, 51818

Product

Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818

Reason for recall

Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.

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-1698-2023. 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.