Hoffmann LRF-Hinge Coupling (2018-03-02)

Starting date:

March 2, 2018

Posting date:

April 3, 2018

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

Healthcare Professionals, Hospitals, General Public

Identification number:

RA-66312

• Reason
• Affected products

Affected products

HOFFMANN LRF-HINGE COUPLING

Reason

Stryker has become aware that some of the hinge coupling packaging may contain incorrect product. This issue was first discovered via customer complaint November 17, 2017 where it was reported that upon opening the 4933-0-800 [lot# 23745] it was discovered that the packaging contained product # 4933-1-011 [lot# 19865]. This Product Field Action (PFA) applies to all unopened/originally packaged products.

Affected products