GUNTHER TULIP RETRIEVAL SET (2021-04-08)

Starting date:

April 8, 2021

Posting date:

April 22, 2021

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-75439

Last updated:
2021-04-22

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  Reason
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  Affected products

Affected Products 

GUNTHER TULIP RETRIEVAL SET

Reason

Cook Inc. has identified that these lots may contain an 0.038" wire guide instead of the specified 0.035" wire guide, resulting in an incompatibility with the supplied dilator (dilator cannot be advanced over the wire guide).

Affected products