Health product recall

Cardinal Health Presource Kits

Last updated

Summary

Product
Cardinal Health Presource Kits
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

SBA30LBNHE

Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

26-0939A

Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

SAN30LPGBD

Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

SBA30LBNHF

Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

SBA30LBYCC

Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

SBA30LBRMB

Arthrogram Pack

More than 10 numbers, contact manufacturer.

SOP30AR25C

Obstetrics And Gynaecology (Ob/Gyn) Packs

424981

07-5687A

Myelogram Pack

326116

27-5687A

Safety Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

SOP30LP11C

Safety Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

SOP30LP01C

Safety Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

SOP30LPHRC

Safety Lumbar Puncture Packs

More than 10 numbers, contact manufacturer.

SOP30LP06C

Issue

Cardinal Health Presource® has identified various kits that may contain a component impacted by the welmed, extension tubing sets component. that advisory was issued to inform customers of a product condition identified in certain lots and to provide inspection and use instructions to help ensure affected product is identified prior to patient use.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Health products - Medical devices - Orthopaedics
Companies
Cardinal Health 200, Llc Also Trading As Cardinal Health
3651 Birchwood Drive, Waukegan, Illinois, United States, 60085
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82747

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