Recall database

Catheter, Urethral recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–2 of 2 recalls

Class IIOngoingZ-2998-2026

Hollister Ulc recalls Onli 17cm Hydrophilic Urethral Intermittent Catheter

Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might lead to genitourinary trauma or bleeding.

Urethral Catheter
Process control

Hollister UlcSep 2, 2026

Class IIOngoingZ-1061-2026

HANGZHOU BEVER MEDICAL DEVICES CO., LTD. recalls BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip

Labeling error, Incorrect expiration date

Urethral Catheter
Labeling Change Control

HANGZHOU BEVER MEDICAL…Jan 21, 2026