No image published for this recall

No image published for this recall

Aesculap Implant PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU - safety alert

Official notice

6 Oct 2021

Last checked

6 Oct 2021

Medium riskFDA

An official FDA notice concerns Aesculap Implant PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU - safety alert. An official FDA notice concerns PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-10-06. Recall numbers: Z-2578-2021. Check the official notice for the complete list. Published 2021-10-06.

What to do now

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

Units affected

80

Recall number

Z-2578-2021

Official notice

2021-10-06

The hazard

An official FDA notice concerns PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-10-06. Recall numbers: Z-2578-2021. 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.

Event Ids

88327

Recall Numbers

Z-2578-2021

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Affected products

Product 1

PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU

Units affected

80

Risk / hazard

An official FDA notice concerns PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-10-06. Recall numbers: Z-2578-2021. 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 · PA · Center Valley

Affected area 1

US · United States · PA · Center Valley

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Aesculap Implant. Contact: Aesculap Implant Systems LLC.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-2578-2021

Event id

88327

Units affected

80

Status

terminated

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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