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Aesculap - safety alert

Official notice

19 Mar 2025

Last checked

19 Mar 2025

Medium riskFDA

An official FDA notice concerns Aesculap - safety alert. An official FDA notice concerns Aesculap. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-03-19. Recall numbers: Z-1308-2025. Check the official notice for the complete list. Published 2025-03-19.

What to do now

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

Units affected

19,979

Recall number

Z-1308-2025

Official notice

2025-03-19

The hazard

An official FDA notice concerns Aesculap. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-03-19. Recall numbers: Z-1308-2025. 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

96223

Recall Numbers

Z-1308-2025

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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. Contact: Aesculap Inc.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-1308-2025

Event id

96223

Units affected

19,979

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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