FDA Device recall Z-1700-2023
Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G
- FDA Device
- Class II
- ongoing
- Published 2023-06-14
On 2023-06-14 the FDA classified a Class II recall of Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G by C R Bard, citing 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 c….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1700-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-04-20 |
| Published | 2023-06-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | C R Bard |
| Distribution | n/a |
Product
Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G
Reason
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.
Identifiers
| code_info | a) REF 52810G, UDI/DI 00801741136870, Lot Numbers: JUGW1445 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1700-2023%22
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