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Baxter corporation reusable blood pressure cuffs

Official notice

11 Apr 2025

Last checked

11 Apr 2025

Medium riskHealth Canada

An official Health Canada notice concerns Baxter corporation reusable blood pressure cuffs. Baxter Corporation is issuing a voluntary product recall for reusable blood pressure cuffs because the product is labeled "not made with natural rubber latex," however, there is a latex-containing rubber band located around the product Instructions For Use (IFU). Baxter is requesting the return of unopened affected blood pressure cuffs in their packaging. Recall start date: March 20, 2025 Published 2025-04-11.

What to do now

Contact the manufacturer if you require additional information.

Recall number

77253

Official notice

2025-04-11

The hazard

Baxter Corporation is issuing a voluntary product recall for reusable blood pressure cuffs because the product is labeled "not made with natural rubber latex," however, there is a latex-containing rubber band located around the product Instructions For Use (IFU). Baxter is requesting the return of unopened affected blood pressure cuffs in their packaging. Recall start date: March 20, 2025

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

77253

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Affected products

Product 1

Affected products - Cuff, Adult, Lot or serial number - 24-314 & lower, Model or catalogue number - 5082-25 5082-01H 5200-01 4500-02 5082-01 5082-22 5082-22H 5082-43

Product 2

Affected products - Blood Pressure Cuff - Adult - Nylon, Lot or serial number - 24-314 & lower, Model or catalogue number - DS44-11

Product 3

Affected products - Connex Spot Monitor (7300 Series), Lot or serial number - 24-314 & lower, Model or catalogue number - 73WT-B

Product 4

Affected products - Welch Allyn Spot Vital Signs 4400, Lot or serial number - 24-314 & lower, Model or catalogue number - 44WT-B 44XT-B

Product 5

Affected products - Cuff, Child, Lot or serial number - 24-314 & lower, Model or catalogue number - 5082-24 5082-21 5082-42 5082-02

Product 6

Affected products - Cuff, Large, Adult, Lot or serial number - 24-314 & lower, Model or catalogue number - 5082-16 5200-02 5082-26 5082-23 5082-23H 5082-44 4500-03

Product 7

Affected products - Cuff, Infant, Lot or serial number - 24-314 & lower, Model or catalogue number - 5082-03 5082-08

Product 8

Affected products - Gs 777 Int'D Diag Sys W/Panop/Stp, Lot or serial number - 24-314 & lower, Model or catalogue number - 77791-2MPX

Product 9

Affected products - Connex Spot Monitor (7400 Series), Lot or serial number - 24-314 & lower, Model or catalogue number - 74CE-B 74MT-B 74MX-B 74CT-B 74CX-B 74ME-B

Product 10

Affected products - Connex Spot Monitor (7500 Series), Lot or serial number - 24-314 & lower, Model or catalogue number - 75MT-B 75MX-B 75CX-B 75ME-B 75CE-B 75CT-B

Product 11

Affected products - Cuff, Newborn, Lot or serial number - 24-314 & lower, Model or catalogue number - 5082-07

Product 12

Affected products - Cuff, Thigh, Lot or serial number - 24-314 & lower, Model or catalogue number - 5082-45 5082-11 5082-77 5082-78

Product 13

Affected products - Vital Signs Monitor Core, Lot or serial number - 24-314 & lower, Model or catalogue number - 75RT-B

Product 14

Affected products - Gold Series DS66 Trigger Aneroids, Lot or serial number - 24-314 & lower, Model or catalogue number - 5098-30 5098-27 5098-28 5098-29

Product 15

Affected products - Silver Series DS45 Integrated And Pocket Aneroids, Lot or serial number - 24-314 & lower, Model or catalogue number - DS45-11 DS45-12 DS45-11C DS45-MC

Product 16

Affected products - Platinum Series DS58 Hand Aneroids, Lot or serial number - 24-314 & lower, Model or catalogue number - DS58-PD DS58-11 DS58-MC

Product 17

Affected products - Bronze Series DS44 Integrated And Pocket Aneroids, Lot or serial number - 24-314 & lower, Model or catalogue number - DS44-09 DS44-11C DS44-MC

Risk / hazard

Baxter Corporation is issuing a voluntary product recall for reusable blood pressure cuffs because the product is labeled "not made with natural rubber latex," however, there is a latex-containing rubber band located around the product Instructions For Use (IFU). Baxter is requesting the return of unopened affected blood pressure cuffs in their packaging. Recall start date: March 20, 2025

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: Welch Allyn, Baxter Reusable Blood Pressure Cuffs.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

77253

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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