No image published for this recall

No image published for this recall

Baxter Healthcare Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis - safety alert

Official notice

27 Nov 2024

Last checked

27 Nov 2024

Critical riskFDA

An official FDA notice concerns Baxter Healthcare Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis - safety alert. An official FDA notice concerns Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2024-11-27. Lots: /Serial. Recall numbers: Z-0375-2025. Check the official notice for the complete list. Published 2024-11-27.

What to do now

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

Units affected

151,020

Recall number

Z-0375-2025

Official notice

2024-11-27

The hazard

An official FDA notice concerns Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2024-11-27. Lots: /Serial. Recall numbers: Z-0375-2025. 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.

Lots

/Serial

Event Ids

95525

Recall Numbers

Z-0375-2025

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Affected products

Product 1

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis

Units affected

151,020

Risk / hazard

An official FDA notice concerns Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2024-11-27. Lots: /Serial. Recall numbers: Z-0375-2025. 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 · IL · Deerfield

Affected area 1

US · United States · IL · Deerfield

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Baxter Healthcare. Contact: Baxter Healthcare Corporation.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

critical

Recall details

Recall number

Z-0375-2025

Event id

95525

Units affected

151,020

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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