C.R. Bard Inc: Medical Device Recall in 2023 - (Recall #: Z-1701-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818

Product Classification:

Class II

Date Initiated: April 20, 2023

Date Posted: June 14, 2023

Recall Number: Z-1701-2023

Event ID: 92082

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.

Status: Ongoing

Product Quantity: 308520 devices

Code Information:

a) REF 71808, Lot Numbers: JUGU9026; b) REF 71810, Lot Numbers: JUGT9154, JUGU9053, JUGV9130, JUGV9133; c) REF 71812, Lot Numbers: JUGT0236, JUGT1689, JUGT2702, JUGU1955, JUGU1968, JUGV9158; d) REF 71814, Lot Numbers: JUGT3326; e) REF 71816, Lot Numbers: JUGU9023; f) REF 71818, Lot Numbers: JUGT0288, JUGU9022

Distribution Pattern:

Worldwide

Voluntary or Mandated:

Voluntary: Firm initiated