FDA Recall Open, Classified

Chromophare Surgical Light System , REF CH00000001

Recall: Z-1506-2024 · Initiated February 8, 2024

Recall

Recall Number
Z-1506-2024
Event Number
94199
Firm
Stryker Communications
FEI Number
3002975342
Product Code
FSY
Status
Open, Classified
Root Cause
Employee error
Initiated
February 8, 2024
Posted
April 9, 2024
Address
571 Silveron Blvd, Flower Mound, TX, 75028

Description

Chromophare Surgical Light System , REF CH00000001

Reason

Due to insufficient mounting force the stability of surgical light system cannot be guaranteed.

Action

On February 19, 2024, Stryker issued a Urgent Medical Device Recall notification via XXX. In addition to notifying consignees about the recall. Stryker asked consignees to take the following actions: Inform individuals within your organization who need to be aware of this action. 2. Check your internal inventory to locate the product listed in the product affected grid. If affected product is found, segregate and do not use the product. 3. Complete and sign the enclosed Business Reply Form on Attachment A and return to [email protected]. 4. A Sales Representative or Field Service Technician will be in contact with your facility to schedule a service visit to perform the recall activities. 5. Maintain awareness of this communication internally until all required actions have been completed within your facility. Response is required.

Distribution

US: None OUS: Chili

Quantity

1 unit