The Recall Desk
HighFDA (Devices)·Z-2539-2019·Announced 2019-09-18

Stryker Recalls Berchtold Chromophare F528 Surgical Lights Due to Assembly Defect

Stryker is recalling 946 Berchtold Chromophare F528 surgical lights because the back cover of the light head was insufficiently assembled and could fall off.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a risk-of-harm product (medical device) where injury has not yet been reported, fitting the criteria for a High severity score.

Plain-English summary

Stryker Communications is recalling 946 units of Berchtold Chromophare F528 Surgical Lights. These medical lights are used in hospital treatment rooms to provide localized lighting for detecting and treating disease, injury, and disability.

The recall was initiated because the back cover of the light head was insufficiently assembled and could potentially fall off the light. The affected serial number ranges are 83180-69712678 to 83180-88970377.

Distribution was nationwide, including to Puerto Rico, as well as government/military distribution. Foreign distribution included Argentina, Austria, Australia, Belgium, Bulgaria, Canada, China, Colombia, Denmark, France, Germany, Hong Kong, India, Indonesia, Italy, Japan, Kazakhstan, Korea, Kuwait, Lithuania, Mexico, Netherlands, Philippines, Poland, Russia, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Taiwan, United Arab Emirates, United Kingdom, Uruguay, and Vietnam. The source text does not specify instructions for consumers or healthcare facilities on how to proceed with the recall.

The recalled product

Product
Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment rooms. They provide localized lighting focused on the patient s body for detecting and treating disease, injury, and disability. The surgical lights may only be
Affected units
946

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Serial number ranges: 83180-69712678 to 83180-88970377

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 2 recalled by Stryker Communications under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →