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Minicap disconnect cap with povidone-iodine

Official notice

10 May 2023

Last checked

10 May 2023

High riskHealth Canada

An official Health Canada notice concerns Minicap disconnect cap with povidone-iodine. Baxter Corportation is issuing a recall for certain lots of the Minicap. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. Baxter is expanding the urgent medical device recall to include all lots of Minicap Disconnect Caps, product code 5C4466P, that expire on or before May 31, 2024. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. Recall start date: February 01, 2023 Published 2023-05-10.

What to do now

Contact the manufacturer if you require additional information.

Recall number

72674

Official notice

2023-05-10

The hazard

Baxter Corportation is issuing a recall for certain lots of the Minicap. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. Baxter is expanding the urgent medical device recall to include all lots of Minicap Disconnect Caps, product code 5C4466P, that expire on or before May 31, 2024. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. Recall start date: February 01, 2023

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.

Recall Numbers

72674

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Affected products

Product 1

Affected products - Minicap Disconnect Cap With Povidone-Iodine, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 5C4466P

Risk / hazard

Baxter Corportation is issuing a recall for certain lots of the Minicap. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. Baxter is expanding the urgent medical device recall to include all lots of Minicap Disconnect Caps, product code 5C4466P, that expire on or before May 31, 2024. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. Recall start date: February 01, 2023

Where it was sold

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

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Baxter Healthcare, Minicap Disconnect Cap With Povidone-iodine.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type I

App estimate

high

Recall details

Recall number

72674

Classification

Type I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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