FDA Device recall Z-2386-2015
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 14 Fr, (30/box), Product Code 51614
- FDA Device
- Class II
- terminated
- Published 2015-08-26
On 2015-08-26 the FDA classified a Class II recall of Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 14 Fr, (30/box), Product Code 51614 by C R Bard, citing potential breach of the sterile barrier packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2386-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-07 |
| Published | 2015-08-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | C R Bard |
| Distribution | US |
Product
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 14 Fr, (30/box), Product Code 51614. Intermittent catheter.
Reason
Potential breach of the sterile barrier packaging.
Identifiers
| code_info | Lot Number 73600003, 73600006, 7360007, 73600011, 73600012, 73600013, 73600016, 73600017, 73600020, 73600021, 73600024,…Lot Number 73600003, 73600006, 7360007, 73600011, 73600012, 73600013, 73600016, 73600017, 73600020, 73600021, 73600024, 73600080, 73600081, 73600082, 73600095, 73600096, 73600097, 73600123, 73600124, 73600125, 73600126, 73600144, 73600145, 73600163, 73600164, 73600167, 73600181, 73600196, 73600217, 73600218 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2386-2015%22
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