C.R. Bard Inc: Medical Device Recall in 2023 - (Recall #: Z-1700-2023)

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:

Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G

Product Classification:

Class II

Date Initiated: April 20, 2023

Date Posted: June 14, 2023

Recall Number: Z-1700-2023

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: 5760 devices

Code Information:

a) REF 52810G, UDI/DI 00801741136870, Lot Numbers: JUGW1445

Distribution Pattern:

Worldwide

Voluntary or Mandated:

Voluntary: Firm initiated