FDA Recall Open, Classified

LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.

Recall: Z-1998-2025 · Initiated May 21, 2025

Recall

Recall Number
Z-1998-2025
Event Number
96729
Firm
Jolife AB Scheelevagen 17 Ideon Science Park Lund Sweden
FEI Number
3005445717
Product Code
DRM
Status
Open, Classified
Root Cause
Employee error
Initiated
May 21, 2025
Posted
June 20, 2025

Description

LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.

Reason

Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.

Action

On 05/21/2025, the firm send via certified mail an "URGENT: MEDICAL DEVICE RECALL" Letter to customers informing them that demonstration LUCAS devices were given to customers for use without the proper labeling. These demonstration units are not maintained in a clinically usable state and are not to be loaned to customers or used in a clinical setting. Customer are instructed to: 1. Immediately check their internal inventory to locate the product listed on the attached business reply form, stop usage, and remove them from their point of use. 2. Return the enclosed business reply form by email to [email protected] to confirm receipt of this notification. 3. Upon receipt of the completed business reply form, Stryker will contact customers to arrange for the return and replacement of the affected product(s). 4. Maintain awareness of this communication internally until all required actions have been completed within their facility. Keep this communication close to the affected items until replacement. 5. Inform Stryker if any of the subject devices have been distributed to other organizations. If so, provide contact details so Stryker can inform the recipients appropriately. Any questions or concerns, contact Customer Service +1 800 787 9537, option 2, from 8:00 AM to 7:00 PM (Eastern Time), Monday Friday or by email at [email protected].

Distribution

U.S. Nationwide distribution in the states of IN, MI, OH and TX.

Quantity

5 units