No image published for this recall

No image published for this recall

Coloplast Titan Pump Assembly, Catalog Number 5177701400; inflatable penile Prosthesis - safety alert

Official notice

19 Apr 2023

Last checked

19 Apr 2023

Medium riskFDA

An official FDA notice concerns Coloplast Titan Pump Assembly, Catalog Number 5177701400; inflatable penile Prosthesis - safety alert. An official FDA notice concerns Titan Pump Assembly, Catalog Number 5177701400; inflatable penile Prosthesis. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2023-04-19. Lots: 8904177. Recall numbers: Z-1360-2023. Check the official notice for the complete list. Published 2023-04-19.

What to do now

The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.

Units affected

9

Recall number

Z-1360-2023

Official notice

2023-04-19

The hazard

An official FDA notice concerns Titan Pump Assembly, Catalog Number 5177701400; inflatable penile Prosthesis. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2023-04-19. Lots: 8904177. Recall numbers: Z-1360-2023. Check the official notice for the complete list.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Lots

8904177

Event Ids

91800

Recall Numbers

Z-1360-2023

Checked manually this time?

The app alerts you when a new official recall is published — no searching, no checking back.

Turn on recall alerts

Affected products

Product 1

Titan Pump Assembly, Catalog Number 5177701400; inflatable penile Prosthesis

Units affected

9

Risk / hazard

An official FDA notice concerns Titan Pump Assembly, Catalog Number 5177701400; inflatable penile Prosthesis. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2023-04-19. Lots: 8904177. Recall numbers: Z-1360-2023. Check the official notice for the complete list.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · MN · Minneapolis

Affected area 1

US · United States · MN · Minneapolis

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Coloplast. Contact: Coloplast Manufacturing US, LLC.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-1360-2023

Event id

91800

Units affected

9

Status

active

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
Something wrong on this page?

Related recalls

US
No image published for this recall

a product listed in the official notice - safety alert

High riskFDA2 Dec 2020
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA6 May 2015
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA27 Apr 2016
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA5 Nov 2014
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA29 May 2013

Weekly recall digest

Get next week's recalls before you need them.

One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.

The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.

This recall was published 19 Apr 2023. The next one won't wait for you to search.

RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.