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Aspen Surgical Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101 - safety alert

Official notice

3 Jul 2024

Last checked

3 Jul 2024

Medium riskFDA

An official FDA notice concerns Aspen Surgical Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101 - safety alert. An official FDA notice concerns Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2024-07-03. Lots: 389571. Recall numbers: Z-2221-2024. Check the official notice for the complete list. Published 2024-07-03.

What to do now

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

Units affected

1,900

Recall number

Z-2221-2024

Official notice

2024-07-03

The hazard

An official FDA notice concerns Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2024-07-03. Lots: 389571. Recall numbers: Z-2221-2024. 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

389571

Other

UDI-DI 00840113214006

Event Ids

94778

Recall Numbers

Z-2221-2024

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Affected products

Product 1

Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101

Units affected

1,900

Risk / hazard

An official FDA notice concerns Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2024-07-03. Lots: 389571. Recall numbers: Z-2221-2024. 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 · MI · Caledonia

Affected area 1

US · United States · MI · Caledonia

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Aspen Surgical. Contact: ASPEN SURGICAL.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-2221-2024

Event id

94778

Units affected

1,900

Status

active

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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