CLASS II ONGOING Device recall · Reported 14 Jun 2023 · FDA Enforcement Report

Magic3 Go Intermittent Urinary Catheters, pediatric recalled

C.R. Bard is recalling Magic3 Go Intermittent Urinary Catheters, pediatric. The recall was initiated on 20 Apr 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesa) REF 52810G, UDI/DI 00801741136870, Lot Numbers: JUGW1445

Quantity recalled5760 devices

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1700-2023
FDA event ID: 92082
Recalling firm: C.R. Bard, Covington, GA
Classification: Class II
Status: Ongoing
Recall initiated: 20 Apr 2023
FDA classified: 8 Jun 2023
Reported: 14 Jun 2023
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Sterility
Device type: Heart & Vascular Devices

Timeline

20 Apr 2023	Recall initiated by company
8 Jun 2023	Classified by FDA	+49 days
14 Jun 2023	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

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

Where it was distributed

Worldwide

Questions about this recall

Why was it recalled?

Which lots are affected?

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

Where was it sold?

Worldwide

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 92082

This product is part of a recall event; the main page for the event is HydroSil Go Intermittent Urinary Catheters recalled by C.R. Bard.

Reported	Class	Recall	Company	Reason	Where
14 Jun 2023	CLASS II	HydroSil Go Intermittent Urinary Catheters recalled by C.R. Bard	C.R. Bard	Sterility	GA
14 Jun 2023	CLASS II	Magic3 Go Intermittent Urinary Catheters, Female recalled by C.R. Bard	C.R. Bard	Sterility	GA
14 Jun 2023	CLASS II	Magic3 Go Intermittent Urinary Catheters, male recalled by C.R. Bard	C.R. Bard	Sterility	GA

More recalls from C.R. Bard

All 123

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Device	CLASS II	Products that contain the Pericare Wipes: *Bardex¿ I.C recalled	C.R. Bard	Other	Nationwide
16 Sep 2026Device	CLASS II	Products that contain the Pericare Wipes recalled by C.R. Bard	C.R. Bard	Other	Nationwide
16 Sep 2026Device	CLASS II	Products that contain the Pericare Wipes recalled by C.R. Bard	C.R. Bard	Other	Nationwide
16 Sep 2026Device	CLASS II	Products that contain the Pericare Wipes recalled by C.R. Bard	C.R. Bard	Temperature Abuse	Nationwide
16 Sep 2026Device	CLASS II	Products that contain the Pericare Wipes recalled by C.R. Bard	C.R. Bard	Temperature Abuse	Nationwide

Other Heart & Vascular Devices recalls

All 6,199

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Device	CLASS II	Getinge PVC Thoracic Catheter, Soft PVC Right Angle recalled	Atrium Medical	Potency & Assay	Nationwide
16 Sep 2026Device	CLASS II	Products that contain the Pericare Wipes: *Bardex¿ I.C recalled	C.R. Bard	Other	Nationwide
16 Sep 2026Device	CLASS II	Products that contain the Pericare Wipes recalled by C.R. Bard	C.R. Bard	Other	Nationwide
16 Sep 2026Device	CLASS II	Products that contain the Pericare Wipes recalled by C.R. Bard	C.R. Bard	Other	Nationwide
16 Sep 2026Device	CLASS II	Getinge PVC Thoracic Catheter, Firm PVC Straight recalled	Atrium Medical	Potency & Assay	Nationwide